Puberty Blocker Ban: Invited Expert Submission

I was an academic expert invited to submit expert opinion & evidence to the Autumn 2024 closed consultation on the legal and criminal ban on puberty blockers. I’m one of the experts that Wes has claimed to have listened to in agreeing to make this ban permanent.

Here is my submission:

Proposed changes to the availability of puberty blockers

Question 1: Do you agree with making it permanent?

Strongly disagree.

The current policy has had very significant negative impacts and consequences for trans children, adolescents and their families. It is not evidence based and does not centre the rights, health or well-being of the children and adolescents who are directly impacted.

Question 2: Positive impacts

Absolutely zero. It has had devastating consequences for many trans children, adolescents and families.

Question 3: Negative impacts

As an academic and researcher specialising in transgender children’s health and well-being, I need to highlight my grave concerns with the unevidenced and risky decision to criminalise access to puberty blockers. The law has already led to significant severe harms/negative consequences, with significant risks to the young people directly impacted. Three items are important to note 1) Consequences of denial of blockers 2) Higher risk of alternative medical pathways 3) Wider healthcare differentials.

  1. Consequences of denial of blockers

The current criminalisation of puberty blockers has not considered the serious consequences of denial of blockers to trans adolescents who feel endogenous puberty would be intolerable. Recent research has been conducted with UK trans adolescents using and seeking access to puberty blockers, and their families. These articles were not considered by the Cass Review as they were published in 2022 (the Cass Review only looked at literature published pre-2021). At this point the government needs to take stock of all modern evidence, including that published post 2021. This more recent research highlights the reasons for trans adolescents and supportive families seeking access to puberty blockers. This research substantiates the importance of puberty blockers in safeguarding and protecting trans youth happiness, self-esteem, mental health, and in enabling trans youth to stay in school, socialise with their friends, enjoy their adolescence. It also touches on the known harms where trans youth are forced through a puberty they find intolerable, including drop out from school, not wanting to leave their room, disconnecting from friends, not wanting to leave the house, stopping wanting to speak in public, anxiety, depression, self-harm, losing hope, suppressing food intake to prevent pubertal development, no longer wanting to be alive.

There are highly significant risks to the well-being and happiness of trans youth denied access to healthcare interventions such as puberty blockers. Being forced through a puberty that is deeply traumatic, when there is an effective and safe medication to prevent that, is a deeply significant interventions in a young person’s bodily autonomy, necessitating a very high barrier of justification, a justification that is simply not present in the case of puberty blockers. The known harms of forcing trans adolescents through endogenous puberty against their will have not been considered in making the decision to criminalise puberty blockers. Any policy in this area needs to draw upon effective risk assessments of the known dangers of not having access to puberty blockers.

  • Higher risk of alternative medical pathways

When it comes to abortion, it is recognised that criminalisation does not prevent abortion, it merely prevents safe abortion, pushing individuals towards less safe routes to healthcare. There are clear parallels with criminalisation of puberty blockers, with clear evidence already apparent of adolescents and supportive families being pushed to less safe routes to healthcare. The risks of forcing individuals into less safe options have not been considered in making this law.

Many adolescents and families impacted by the current ban feel that being forced through unwanted endogenous puberty is entirely intolerable and inconceivable, and will navigate any other option to ensure that does not happen. Some are looking to flee the country, literally being driven out of their home by a criminal ban on essential healthcare that is more draconian than anywhere else in the democratic world. Some are applying for asylum, due to being persecuted by their government just for being trans. Some are needing to travel abroad every three months in order to access healthcare outside of the UK. This is a significant financial burned on supportive families, and a significant burden and stress on those adolescents who should be able to access healthcare locally, who should be able to spend their weekends having fun with their friends rather than travelling outside of the UK to maintain their right to bodily autonomy and a happy adolescence. Others are likely accessing the Black market, with risks especially related to a lack of blood hormone monitoring and medical oversight. Many are switching from puberty blockers to non-criminalised alternative medication that has a similar impact on preventing puberty, medication that is known to have greater side effects than puberty blockers. In the decision to criminalise puberty blockers, a medication known to be safe, there has been zero consideration of the risks of the alternative medication that youth are now switching to. Other adolescents are going directly to oestrogen or testosterone, at an earlier age than they would have chosen to do if puberty blockers were available. The current criminalisation is having very significant impacts on the healthcare options and pathways that trans youth are accessing. It is not stopping trans youth from accessing affirmative healthcare, merely pushing youth towards options that are less safe.

  • Wider healthcare differentials

A significant impact of criminalisation is a very significant rise in trans children, trans adolescent and supportive family distrust of healthcare providers including GPs. Adolescents and supportive families forced into less ideal paths to healthcare to avoid criminalisation also now have significant reasons to avoid engagement with their local GP. I am deeply concerned about the wider health impacts, both short and long-term, of having a population who are avoiding routine healthcare interactions with their GP and other healthcare providers, related to current criminalisation. This is and will continue to feed into wider healthcare differentials and poorer healthcare outcomes far beyond trans health.

References on puberty blockers (peer reviewed journal articles)

Horton, C. (2022). Experiences of puberty and ‘puberty blockers’ – Insights from trans children, trans adolescents and their parents. Journal of Adolescent Research.

Horton, C. (2022). “I didn’t want him to disappear” Parental decision-making on access to puberty blockers for trans early adolescents. Journal of Early Adolescence.

Question 4: Benefits

It is extremely dangerous and damaging – making it permanent would magnify and entrench the current harms.

Question 5: Risks and risk mitigation

There is no way of mitigating the current risks. It is deeply dangerous and damaging.

Question 6: Impact on protected groups

It is evidently directly discriminatory against those with the protected characteristics of gender reassignment. The same medication, with the exact same purpose (preventing puberty), is considered safe and not criminalised when used by other groups. The argument that it is not discrimination because use for preventing puberty in trans youth has a separate (outdated) psychiatric diagnosis label is not a credible argument. The same medication, the same purpose (preventing puberty), fine for an individual who is not trans, a criminal offense if they are trans. Absolutely direct discrimination.

Looked after children/children in care are being disproportionately negatively impacted by the current criminalisation. The impact of the current criminalisation is being unevenly carried. There are systemic inequalities in which adolescents are being forced to medically de-transition and forced through a endogenous puberty they find intolerable. I am particularly worried about those least able to circumnavigate current criminalisation, especially looked after children. Whilst many other youth with supportive families find some alternative route to avoid being forced through an intolerable puberty, looked after children, even those with supportive carers, are least able to find a route through. The burden of this criminalisation, and its heavy expected negative impacts on trans youth, is falling most heavily on those who are already disadvantaged through being in the care system. Criminalisation is a very blunt instrument for healthcare, and it is particularly blunt in its impact on trans youth in care who desperately need to avoid being forced through an endogenous puberty. There need to be pathways for individualised healthcare, without the law providing a blanket barrier to providing individualised healthcare to each child and adolescent.

Question 7: Additional evidence

As an academic and researcher specialising in transgender children’s health and well-being, I need to highlight my grave concerns with the unevidenced and risky decision to criminalise access to puberty blockers. In addition to the severe harms/negative consequences, and significant risks of criminalising access to puberty blockers outlined above, I will here highlight five serious flaws and miscalculations that have influenced this poor policy, relating to 1) puberty blocker effectiveness 2) safety 3) erosion of child rights and healthcare ethics 4) Pathologisation & mental health led approaches to trans healthcare 5) Government interference in healthcare.

  1. Puberty Blocker Effectiveness.

Puberty blockers are extremely effective at their primary purpose – stopping puberty. Their effectiveness is well studied and not in doubt. Supposed concerns about a lack of evidence of the ‘benefit’ of puberty blockers fail to engage with a critical question. Are they effective at stopping puberty (answer – yes – this is beyond doubt). Trans healthcare scholars and gender service users are very clear that the key purpose of puberty blockers is to prevent endogenous puberty, preventing the progression of unwanted secondary sexual characteristics. Puberty blockers are not expected to resolve ‘gender dysphoria’, where gender dysphoria is a psychiatric diagnosis under the DSM-V that proxies being trans. Puberty blockers are not expected to lead to an improvement in mental health and well-being, they are intended to prevent the catastrophic decline in mental health and well-being that is known to occur when trans youth are forced through a puberty they find intolerable. Discussions on a lack of evidence of puberty blockers resolving gender dysphoria or improving mental health are, at best, a severe misunderstanding of trans youth healthcare. Their purpose is to prevent puberty, and at this they are undoubtably highly effective.

  • Safety

Puberty blockers have been used and studied in different populations for many decades, including use in trans adolescents since 1988. There is no evidence of significant safety concerns when used in trans or non-trans patients. The medication does not work any differently in trans compared to non-trans patients, having the exact same purpose in preventing puberty. There can be different reasons for wanting to prevent puberty (for precocious puberty it is to delay puberty to align with ones peers, for trans adolescents it is for bodily autonomy and preventing progression of a puberty they find intolerable and incompatible with their bodily aspirations, for some cancer treatment it is to remove sex hormones that impact on their cancer). The reasons for stopping puberty are different, but the medication is equally safe. Here the medication is permitted for all uses to prevent puberty in cis (non-trans) people, and is only deemed unsafe for trans people. There is zero evidence that puberty blockers work in a different manner in trans versus cis bodies. There is zero evidence that the same medication, for the same purpose (preventing release of endogenous sex hormones), is somehow safe in cis people an unsafe in trans people. There has been no documented evidence of serious risk in use of this medication, certainly nothing to justify criminalisation.

The known risks of puberty blockers can be monitored and minimised as part of standard endocrine care. Bone health can be monitored, with exogenous sex hormones provided before bone health is compromised, alongside recommendations for exercise and vitamin supplements. There is simply no evidence of any serious safety concern.

The only current suggested harms of puberty blockers for trans youth fall into a category of ‘speculation and pseudoscience’. The Cass Review includes an unevidenced statement speculating that puberty blockers may change the outcome, preventing trans children from shifting into cis identities in adolescence. Trans scholars and healthcare professionals have raised very significant concerns about the Cass, as written in peer reviewed academic publications and scientific commentaries. The Cass Review’s unevidenced speculation on blockers potentially keeping trans children as trans is a gross misunderstanding of existing scholarship on this topic. There is no such evidence that trans children denied puberty blockers become cis youth, or that puberty blockers have any impact on identity. This speculation of a psychological impact of puberty blockers on identity is entirely unsubstantiated, and is in fact directly contradicted by modern evidence that shows trans children frequently grow into trans adults, regardless of healthcare provision or denial. There is zero credible evidence that puberty blockers, a medication used on cis children without any anticipated impact on their gender identity, will have any impact on identity in trans people.

The second speculated ‘risk’ of puberty blockers, is the suggestion that there are ‘unknown’ impacts on brain development. Again, this is entirely unevidenced and speculative. Puberty blockers have been used for many decades, including for trans youth since 1988, with no recorded negative impacts on brain development. Speculation should not be substantiating a highly unusual decision to criminalise a medication. Especially when that speculation is only used to criminalise use of a medication in a highly persecuted minority, while leaving the same medication available to all other populations.

  • Erosion of child rights and healthcare ethics

The current criminalisation of puberty blockers runs in the face of core concepts of child rights, bodily autonomy and healthcare ethics. Decisions on this topic need to bring ethics and healthcare rights into much greater focus. This also needs to consider the reality that puberty blockers are supposedly criminalised apart from for youth under a proposed NHS trial. This trial is not yet designed nevermind launched, with youth being forced to navigate alternative routes to healthcare while waiting for said trial. There are also very significant ethical concerns about the proposed trial, in a UK gender service that has long been critiqued for severe ethical failings. Many many families will not force their child through a service and trial that has significant ethical failings, and currently criminalisation is one tool being used to coerce children into such an unethical trial.

I am also deeply concerned that the proposed criminalisation on puberty blockers is being pushed through without effective and meaningful listening to the adolescents most directly impacted, and their caregivers and Doctors. I am concerned that the latest policy proposal document dismisses the need for further stakeholder consultation, claiming that the Cass Review itself “include(ed) extensive stakeholder engagement with those with ‘lived experience’”. Any engagement with trans communities in the UK will quickly reveal a very widespread belief that Cass Review stakeholder engagement did not meaningfully inform the final report, with community, academic and professional critiques of the Cass process and outcomes extensive, well-documented and growing. Trans communities and trans adolescents have a right to a seat at the table in influencing trans healthcare policy, and this current criminalisation is yet another in a long series of processes where lived experience voices are not being heard or listened to. If the government has any care for trans children and young people, there needs to be a process of committed rebuilding of faith with trans communities, including a commitment to ensuring lived experience specialists are given a seat at the table in informing trans healthcare policy and legislation. 

Current policy documents fail to even recognise the scale of the impact on trans youth. Several documents convey the impression that youth currently accessing puberty blockers are unlikely to be forced to medically de-transition. In reality, the vast majority (over a thousand) trans adolescents currently in receipt of puberty blockers at the point of the introduction of the ban found themselves immediately without any legal route to continue their prescription, and facing an immediate risk of medical de-transition, a forced medical de-transition known to have significant psychological and well-being risks. There has been no estimation of the scale of impacts on trans children who have entered into puberty in the months since the criminal ban, and no estimation on the psychological toll, fear and distress of trans children approaching puberty. The government has taken no effort to understand the experiences and impacts on trans children and adolescents.  

  • Pathologisation & mental health led approaches to trans healthcare

I am also deeply concerned that the proposed policy document references the “importance of ensuring that children and young people impacted by the order can access appropriate support”. Noticeably this does not specify what ‘support’ is effective and appropriate for a child or adolescent who is being forcibly medically detransitioned or who is being coerced through a puberty they find intolerable. This oversight, and the failure to consider what is “appropriate support” in lieu of affirmative healthcare is a fundamental and deep rooted flaw in this whole approach. There is no approach to support for trans adolescents with more evidence of effectiveness than affirmative healthcare, including access to puberty blockers and HRT. The government is criminalising the best currently available healthcare. There is no evidence that alternative medication to treat the symptoms of denial of trans healthcare (including anti anxiety and anti depression medication, or psychotherapy) is effective for trans youth wanting to avoid distressing pubertal changes. I am deeply concerned that the government policy is paying lip service to “support” to those children and adolescents affected by criminalisation, whilst having no evidence-based support to offer.

In managing the ‘risks’ to trans children and adolescents denied affirmative healthcare, the current consultation places significant emphasis on ‘access to mental health services’. There is significant evidence of pathologisation of trans identities in this approach. Trans children and adolescents, when supported and provided access to affirmative healthcare, may not ever need access to mental health services. The assumption that mental health services are needed by trans children and adolescents is worrying, especially when the mental health need to be managed, is the need directly caused by a UK government ban on essential healthcare. The NHS is supposed to have switched from the view of transness as a mental health disorder as categorised in older healthcare standards, through to acknowledgement that trans-ness is not a mental health condition but a natural part of human diversity, as categoried in the World Health Organisation’s ICD-11. The NHS is yet again failing in its supposed commitments to depathologisation of trans identities, proposing mental health led care for trans young people. This is an extremely dangerous and harmful approach.

  • Government interference in healthcare

I am very concerned about political interference in healthcare, especially when targeting a persecuted minority. There needs to be an exceptionally high bar of justification for political interference in healthcare, especially for use of a blunt instrument like a criminal ban on a medication only when used by a minority population. Trans scholars and communities have long flagged the serious injustices, misunderstandings, and structural violence in navigating healthcare services that fail to provide equitable healthcare to trans people. Here, the government has taken a step to criminalise an aspect of healthcare that is strongly supported by many healthcare professional bodies worldwide. Doctors are being prevented from making individualised decisions with their patients. The law is a very crude tool and politicians stepping between Dr and patient need to be very confident that the risk clearly merits this intervention, bearing in mind also the expected risks of criminalisation. In this case the risk of puberty blockers is entirely unsubstantiated, indeed they are deemed safe for every other population group, and are deemed safe enough for an NHS trial. The statement in the equality and impact assessment that this criminalisation does not directly discriminate against people with the protected characteristic of gender reassignment is entirely uncredible. The policy very clearly directly discriminates against use of puberty blockers only when used by trans adolescents. Children using them for the exact same purpose (preventing puberty), are not criminalised, if they are not trans. The risks of criminalisation are already very clear and growing by the day, pushing trans adolescents towards routes that are known to be less safe than puberty blockers. The policy does not stand up to scrutiny as necessary or evidence based. It is not driven by any understanding of trans adolescents nor care for their rights and well-being. It is not informed by engagement with trans healthcare experts. It will certainly go down in history as an example of government persecution of trans communities. Healthcare should be individualised and evidence based, with no room for prejudice. Criminalisation of a medication only when used by trans adolescents is a very clear example of prejudice informed healthcare.  

References

On failings in the Cass Review (peer reviewed journal article)

Horton, C. (2024) The Cass Review:  Cis-supremacy in the UK’s approach to healthcare for trans children. International Journal of Transgender Health

On failings in the Cass Review (commentary)

Horton, C. and Pearce, R. (2024) The U.K.’s Cass Review Badly Fails Trans Children, Scientific American

Pearce, Ruth (2024) What’s wrong with the Cass Review: A round up of commentary and evidence. Blog post.

Horton, Cal (2024). “Social transition, puberty blockers and the Cass Review”, What the Trans Podcast: https://whatthetrans.com/social-transition-puberty-blockers-and-the-cass-review-podcast-transcript/

On ethical failings in trans healthcare services in the UK (peer reviewed journal articles)

Horton, C. (2021) “It felt like they were trying to destabilise us”:  Parent assessment in UK Children’s Gender Services, International Journal of Transgender Health

Horton, C. (2022). “Of Course, I’m Intimidated by Them. They Could Take My Human Rights Away”: Trans Children’s Experiences with UK Gender Clinics. Bulletin of Applied Transgender Studies.

Horton, C. (2022). De-pathologising diversity: Trans children and families’ experiences of pathologisation in the UK. Children and Society.

On the need for child voice and child rights in healthcare research and policy (peer reviewed journal articles)

Horton, C. (2024) The importance of child voice in trans health research: a critical review of research on social transition & well-being in trans children. International Journal of Transgender Health

Horton, C., Pearce, R., Veale, J., Oakes-Monger, T. C., Pang, K. C., Pullen Sansfaçon, A., & Quinney, S. (2024). Child rights in trans healthcare – a call to action. International Journal of Transgender Health, 25(3), 313–320.

On the need for depathologisation of healthcare (peer reviewed journal article)

Horton, C. (2022). De-pathologising diversity: Trans children and families’ experiences of pathologisation in the UK. Children and Society.

Question 8: Data gathering

There is no way to gather meaningful data on those trans children, adolescents and supportive families directly harmed by this law without trust. Currently the UK government hold no such trust amongst impacted communities, who view this current criminalisation as a direct attack on trans children’s rights, lives and well-being. Without trust building, people will continue to be afraid to engage with government or NHS related data collection on this topic. Trust needs to be earned through removal of this harmful attach on trans children and adolescents, through ensuring lived experience experts are given an influential and respected seat at the table in government and NHS policy spheres, and through enacting policy that is actually guided by listening to and ensuring the best interests of trans children and young people.

Question 9: Satisfaction with consultation

Very little faith that this consultation will be listened to, or that the harms to trans children will carry weight in the eyes of those making decisions.

Latest Evidence on Puberty Blockers

In 2020 I summarised the then published research on puberty blockers in a blog. That blog post remains a comprehensive overview of the pre 2020 literature, with relevance to discussions today.

There has been a significant body of research on puberty blockers published since that 2020 blog, that I will summarise and keep updated here. I’ve been meaning to update that blog, 4 years later. I was given encouragement by the latest overstep by the Charity Commission.

Yesterday the UK Charity Commission insisted that UK Charities revise their communication on puberty blockers with due regard for the findings of the Cass Review. This Charity Commission recommendation is problematic for two major reasons. Firstly, the Cass Review was heavily biased, an exemplar of prejudice impacting on healthcare policy, and has been widely condemned by trans communities, by healthcare experts worldwide and by academic researchers. The Charity Commission has no business stepping into this realm of academic criticism, and should not be preventing UK charities from highlighting the areas where the Cass Review deviated, for ideological reasons, from the evidence base. UK charities should not be coerced by the Charity Commission to endorse and disseminate medical advice they know to be deeply flawed. (Ruth Pearce has also done a blog on the Charity Commission’s latest advice to UK charities).

Secondly, regardless of any view on the reliability of the Cass Review, the Cass Review presents a snapshot of scientific evidence review at one point in time. The Cass Review drew upon a systematic review that looked at evidence published before April 2022 (and omitted some evidence published before that). The Cass Review was very clear that the science and evidence base underpinning trans youth healthcare is evolving and growing, and that approaches need to be atuned to new evidence as it is published. Science does not stand still. We need to continue to track and report on new evidence as it becomes available. Charities and others advising and supporting trans youth need to ensure they are representing current literature and current knowledge on puberty blockers, including considering the numerous peer reviewed academic studies published since April 2022.

This blog summarises all the literature published on puberty blockers since my last blog (written in early 2020). Many of the more recent of these articles were not considered by the Cass Review. The Cass Review examined articles published before April 2022 – articles published since that date are starred to highlight the evolving evidence base in this field.  

(note: The April 2022 cut-off date was used variably by the Cass Review. April 2022 was stated as the cut-off date for inclusion of studies in the York systematic literature review – however the Cass Review did include more recent studies that were critical or ambivalent about gender affirmative care, whilst ignoring more recent studies that presented positive findings on gender affirmative care).

On effectiveness

Mejia-Otero et al. (2021) “Effectiveness of Puberty Suppression with Gonadotropin-Releasing Hormone Agonists in Transgender Youth. Found that puberty blockers were effective at blocking puberty, and as effective in trans youth as in cis youth with precocious puberty.

On mental health

*Chen et al. (not yet published). This study was presented at WPATH 2024. It highlighted the different mental health trajectories of trans youth. It emphasised that for trans youth with childhood support, family support, affirmation, low levels of gender minority stress, they have good mental health from childhood, and that good mental health is maintained through puberty blocker and gender affirming hormone treatment. For these youth, puberty blocker treatment would not lead to an improvement in mental health but a retention and protection of that good mental health. This is a very important distinction and highlights that looking for ‘mental health improvements’ is the wrong metric for this cohort. Similarly it highlighted a group with persistent mental health challenges, throughout gender affirming treatment. It concluded that gender affirmative healthcare is an important component of healthcare, but not expected to eradicate mental health challenges, especially for trans youth facing hostility, hate and persecution, and for youth with co-existing challenges linked to elevated rates of mental health. Overall, amongst youth receiving gender affirming healthcare, good mental health was more likely in trans youth with less loneliness, less gender minority stress, higher parental acceptance and higher emotional support.

* Kuper et al. (not yet published). This study was presented at WPATH 2024. It examined the outcomes for trans youth receiving testosterone and oestrogen. It noted that large improvements in body dissatisfaction were seen as the primary goal of treatment. This is an important clarification of a key goal of gender affirming care. It noted modest improvements in mental health and quality of life, which were also impacted by gender minority stress. They noted that this sample is in Texas where there are very significant socio-political stressors and state persecution, which is likely impacting on mental health measures. This study again emphasises that mental health does not operate in a vacuum, and that looking for improvements in mental health may be an unhelpful metric in a context where trans youth face severe and chronic stressors.

 *McGregor et al. (2024) “Association of Pubertal Blockade at Tanner 2/3 With Psychosocial Benefits in Transgender and Gender Diverse Youth at Hormone Readiness Assessment”. It compared 40 trans adolescents receiving blocker at tanner 2 or 3 to 398 trans adolescents who had not accessed a puberty blocker. It found those who accessed a puberty blocker had lower anxiety, less depression, less stress, and were significantly less likely to report any suicidal thoughts.

*Horton (2022) [My article] “Experiences of Puberty and Puberty Blockers: Insights From Trans Children, Trans Adolescents, and Their Parents”. Three major themes are presented, relating to pre-pubertal anxiety; difficulties accessing blockers; and, for a minority who were on blockers, experiences of relief and frustration. It highlighted the increase of anxiety in the years before puberty, and the role of confidence that puberty blockers would be available in assuaging that anxiety. This is one of the only pieces of modern research that actually centres trans children’s voices and perspectives on puberty blockers.

Chen et. al (2021) “Psychosocial Characteristics of Transgender Youth Seeking Gender-Affirming Medical Treatment: Baseline Findings from the TYC Study”. It compared the well-being of 95 trans adolescents just before accessing puberty blockers (mean age 11) to the well-being of 316 trans adolescents just before accessing HRT (mean age 16). A vast majority (93%) of the youth just about to start HRT had not been able to access puberty blockers. This study compared the two groups. Amongst the group about to access puberty blockers 28% showed depression, 22% anxiety, 23% lifetime suicidal ideation and 7.9% a past suicide attempt. Amongst the group about to access HRT group, the vast majority of whom had not been able to access puberty blockers 51% showed depression, 57% anxiety, 66% suicidal ideation and 24% a past suicide attempt. The study may indicate a decline in well-being over adolescence for trans youth who are not able to access affirmative healthcare, pointing to possible benefits of accessing gender-affirming treatment earlier in life. 

*Tordoff et al. (2022) “Mental Health Outcomes in Transgender and Nonbinary Youths Receiving Gender-Affirming Care”. The study looked at 104 trans youths. It found that receipt of gender-affirming care, including puberty blockers and gender-affirming hormones, was associated with 60% lower odds of moderate or severe depression and 73% lower odds of suicidality over a 12-month follow-up. Given this population’s high rates of adverse mental health outcomes, these data suggest that access to pharmacological interventions may be associated with improved mental health among TNB youths over a short period.

Wittlin et al. (2024) “Mental Health during Medical Transition in a US and Canadian Sample of Early Socially Transitioned Transgender Youth“. Looked at anxiety and depressive symptoms among transgender youth at 3 stages: before youth had begun puberty blockers; after they had begun blockers; and after they had begun hormone therapy, comparing them to samples of cis youth. In this sample of transgender youth who sought and received gender-affirming medical care, participants experienced stable and relatively low levels of psychological distress across stages of medical transition and across time. There was one exception: transgender girls showed increased, followed by decreased, parent-reported depressive symptoms over time. In contrast, cisgender girls showed increases in internalizing symptomatology (with the exception of parent-reported anxiety) as they got older, and cisgender boys showed decreased self-reported anxiety and increased, followed by decreased, parent-reported depressive symptoms. By mid-adolescence, levels of anxiety and depressive symptoms among transgender girls and transgender boys generally fell between those of cisgender girls and cisgender boys.

On quality of life & well-being

Fontanari et al. (2020) “Gender Affirmation Is Associated with Transgender and Gender Nonbinary Youth Mental Health Improvement”. Survey of 350 Brazilian trans youth. Having accessed multiple steps of gender affirmation (social, legal, and medical/surgical) was associated with fewer symptoms of depression and less anxiety. Furthermore, engaging in gender affirmation processes helped youth to develop a sense of pride and positivity about their gender identity and a feeling of being socially accepted.

Carmichael et al. (2021) “Short-term outcomes of pubertal suppression in a selected cohort of 12 to 15 year old young people with persistent gender dysphoria in the UK”. Research of 44 trans youth. Overall patient experience of changes on GnRHa treatment was positive. It identified no changes in psychological function. Bone mass density was as expected.

Becker-Helby et al. (2020) “Psychosocial health in adolescents and young adults with gender dysphoria before and after gender-affirming medical interventions: a descriptive study from the Hamburg Gender Identity Service”. Followed 75 German trans youth from baseline through to 2 years later. 21 had no medical interventions. 11 had puberty suppression only. 32 had gender affirming hormones only. 11 had gender affirming hormones and surgery, predominantly mastectomy. At baseline all groups had high anxiety and low quality of life scores. For the puberty suppression group, quality of life measures at follow up after 2 years matched German healthy norms. Clinicians’ ratings of global functioning (CGAS) indicated good functioning levels at follow-up. Rates of anxiety and depression were still elevated.

*Horton (2022) [My article] ““I Didn’t Want Him to Disappear” Parental Decision-Making on Access to Puberty Blockers for Trans Early Adolescents”. This looked at how 30 parents of trans children navigate decisions about puberty blockers, and what factors those parents see as important for their children’s health and well-being. Parents regarded puberty blockers as protective of short and long term mental health. They felt puberty blockers enabled and sustained adolescent well-being and quality of life, enabling trans youth to focus on education, socialising, friendships, enjoying their adolescence. Parents expressed frustration at an excessively onerous process for providing consent, in particular the practice of asking adolescents at the point of accessing puberty blockers to consider the impacts of other medical interventions like HRT and surgery. Parents felt the process of taking consent should acknowledge that taking puberty blockers for a trans adolescent is not a more significant decision than a decision to proceed through endogenous puberty. Parents expressed dismay at the way in which evidence of safety and effectiveness for cis youth was disregarded (the same drugs do not work differently in trans youth). Parents also commented on they fact that they would never engage in a Randomised Control Trial of puberty blockers, highlighting significant practical and ethical flaws.

Impact on bodies and future surgery

Van de Grift et al. (2021) “Timing of Puberty Suppression and Surgical Options for Transgender Youth”. Looked at the impact of puberty blocking medication for trans people who later pursue surgical transition. They found that trans masculine adolescents receiving early puberty blockers were less likely to need chest surgery. Trans feminine adolescents receiving early puberty blockers were more likely to require a different type of bottom surgery to trans feminine adolescents who had not received early puberty blockers.

*Boogers et al. 2023 “Time Course of Body Composition Changes in Transgender Adolescents During Puberty Suppression and Sex Hormone Treatment”. Study compared trans girls on puberty blockers to cis boys and trans boys on puberty blockers to cis girls. Trans girls experienced ongoing lean mass decrease and fat mass increase compared to cis boys during 3 years of PS while in trans boys smaller changes compared to cis girls were observed that stabilized after 1 year.

On body image and body satisfaction

‘Bodily satisfaction’ or ‘appearance congruence’ are recognised as a critical outcome or benefit of access to puberty blockers.

*Chen et al. (2023) “Psychosocial Functioning in Transgender Youth after 2 Years of Hormones”. It monitored the impact of 2 years of HRT on 315 trans adolescents (mean age 16). During the study period, appearance congruence, positive affect, and life satisfaction increased, and depression and anxiety symptoms decreased. Increases in appearance congruence were associated with concurrent increases in positive affect and life satisfaction and decreases in depression and anxiety symptoms. The authors note that two trans youth died by suicide during the study period.

Kuper et al. (2021) “Body Dissatisfaction and Mental Health Outcomes of Youth on Gender-Affirming Hormone Therapy”. This study was not specifically on puberty blockers. But highlights that bodily satisfaction is a key measure that is changed through gender affirming hormones.

Grannis et al. (2021) “Testosterone treatment, internalizing symptoms, and body image dissatisfaction in transgender boys”. This study was not specifically on puberty blockers. It examined the well-being and bodily satisfaction of trans boys who had not received puberty blockers, comparing those who accessed Testosterone to those who had not yet accessed Testosterone. Those who had been through puberty without puberty blockers had high bodily dissatisfaction, anxiety and depression. Those on testosterone had reduced bodily dissatisfaction, with lower depression and suicidality. Group differences on depression and suicidality were directly associated with body image dissatisfaction

Articles on the rates of satisfaction with treatment and rates of continuation of gender affirming healthcare after puberty blockers

*Van der Loos et al. (2022) “Continuation of gender-affirming hormones in transgender people starting puberty suppression in adolescence: a cohort study in the Netherlands”. 720 people were included, of whom 220 (31%) were assigned male at birth and 500 (69%) were assigned female at birth. At the start of GnRHa treatment, the median age was 14·1 (IQR 13·0–16·3) years for people assigned male at birth and 16·0 (14·1–16·9) years for people assigned female at birth. Median age at end of data collection was 20·2 (17·9–24·8) years for people assigned male at birth and 19·2 (17·8–22·0) years for those assigned female at birth. 704 (98%) people who had started gender-affirming medical treatment in adolescence continued to use gender-affirming hormones at follow-up. Age at first visit, year of first visit, age and puberty stage at start of GnRHa treatment, age at start of gender-affirming hormone treatment, year of start of gender-affirming hormone treatment, and gonadectomy were not associated with discontinuing gender-affirming hormones. Most participants who started gender-affirming hormones in adolescence continued this treatment into adulthood. The continuation of treatment is reassuring considering the worries that people who started treatment in adolescence might discontinue gender-affirming treatment.

*Cavve et al. (2024) “Reidentification With Birth-Registered Sex in a Western Australian Pediatric Gender Clinic Cohort”. From those seen at this Australian clinic between 2014 and 2020, 1% of trans adolescents accessing medical treatment including puberty blockers later reidentified with their assigned sex when followed up in 2022.

*Van der Loos et al. (2023) “Children and adolescents in the Amsterdam Cohort of Gender Dysphoria: trends in diagnostic- and treatment trajectories during the first 20 years of the Dutch Protocol”. This Study looked at the pathways of children who received puberty blockers over a 20 year period. Of all 266 AMAB who started GnRHa at our center, 9 (3.4%) discontinued treatment. Six (2.3%) ceased treatment because of abating GD. In 2 AMAB (0.8%), GnRHa treatment ended due to psychological or social issues hindering transition. In 1 individual (0.4%), GnRHa was discontinued due to compliance issues. Of all 616 AFAB, 5 (0.8%) broke off GnRHa. In 3 (0.5%), remission of GD led to discontinuation. In 2 (0.3%), GnRHa was suspended due to compliance issues. Of 707 eligible VUmc participants using GnRHa, 93% subsequently started GAH. The majority of people who had not yet started GAH did so for protocol reasons respectively. They were either too young or had not used GnRHa for the required amount of time.

*Masic et al. (2022) “Trajectories of transgender adolescents referred for endocrine intervention in England”. Not very informative.

*Butler et al. (2022) “Discharge outcome analysis of 1089 transgender young people referred to paediatric endocrine clinics in England 2008–2021”. Looked at pathways of those who had accessed endocrine services. 999/1089 (91.7%) continued identifying as gender variant. 90/1089 ceased identifying as gender variant. 58/1089 (5.3%) stopped treatment either with the gonadotropin releasing hormone analogue (GnRHa) or gender-affirming hormones (GAH) and reverted to their birth gender: <16 years (20/217; 9.2%); ≥16 years (38/872; 4.4%). Subdividing further, 16/217 (7.4%) <16 years ceased GnRHa and 4/217 (1.8%) after GAH. Of those ≥16 years, 33/872 (3.8%) ceased GnRHa and 5/872 (0.6%) GAH. At discharge, 91.7% continued as transgender or gender variant, 86.8% sought ongoing care through NHS GICs. 2.9% ceased identifying as transgender after an initial consultation prior to any endocrine intervention and 5.3% stopped treatment either with GnRHa or GAH, a higher proportion in the <16 year compared with the ≥16 year groups. 

On impact of puberty blockers on future sexual functioning

Van der Meulen et al. (2024) “Timing of puberty suppression in transgender adolescents and sexual functioning after vaginoplasty“. Looked at 37 transfeminine individuals treated with a gonadotropin-releasing hormone agonist (puberty suppression), estrogen, and vaginoplasty (penile inversion technique or intestinal vaginoplasty) in the Netherlands, between 2000 and 2016. Experiences regarding sexual functioning and difficulties were assessed with a self-developed questionnaire ~1.5 years after genital gender-affirming surgery and compared between early (Tanner stage G2-3) and late (Tanner stage G4-5) treatment with puberty suppression. Following surgery, 91% of transfeminine individuals was able to experience sexual desire, 86% experienced arousal, and 78% could attain an orgasm. Seventy-five percent of transfeminine individuals who had not experienced an orgasm pre-surgery were able to experience one post-surgery. Of all participants, 62% reported having tried penile-vaginal intercourse post-surgery. The majority reported the presence of one or multiple sexual challenges. There were no significant differences in postoperative sexual function or sexual difficulties between groups treated with early versus late puberty suppression. This study found that post-vaginoplasty transfeminine individuals after both early and late suppression of puberty have the ability to experience sexual desire and arousal, and to achieve orgasms. Outcomes are comparable to previous findings in those who started treatment in adulthood.

Articles examining how puberty blockers impact on other aspects of health

Strang et al. (2021) “Transgender Youth Executive Functioning: Relationships with Anxiety Symptoms, Autism Spectrum Disorder, and Gender-Affirming Medical Treatment Status”. The study looked at executive functioning in 124 trans youth. 21 % of non-autistic and 69 % of autistic transgender youth had clinically elevated EF problems. Autism, anxiety and depression were all associated with lower executive function. Those on just puberty blockers for a year or less saw no impact on executive function. Being on puberty blockers without HRT for more than a year was slightly associated with low executive function. Being on gender-affirming hormones was associated with better executive function. It noted that experiences of stress, rejection and gender minority stress are likely to negatively impact on executive function.

*Valentine et al. (2022) “Multicenter Analysis of Cardiometabolic-related Diagnoses in Transgender and Gender-Diverse Youth: A PEDSnet Study” The study found that GnRHa were not associated with greater odds of cardiometabolic-related diagnoses.

Perl et al. (2021) “Blood pressure dynamics after pubertal suppression with gonadotropin-releasing hormone analogs followed by estradiol treatment in transgender female adolescents: a pilot study”. This research found that being on puberty blockers for trans feminine adolescents did not impact on blood pressure.

Perl et al. (2021) “Blood Pressure Dynamics After Pubertal Suppression with Gonadotropin-Releasing Hormone Analogs Followed by Testosterone Treatment in Transgender Male Adolescents: A Pilot Study”. This research found that being on puberty blockers for trans masculine adolescents had some impact on blood pressure, with this effect disappearing when on testosterone.

Russel et al. (2020) “A Longitudinal Study of Features Associated with Autism Spectrum in Clinic Referred, Gender Diverse Adolescents Accessing Puberty Suppression Treatment”. The research found that for autistic trans youth, being on puberty blockers did not affect their social responsiveness. (?)

Articles related to bone health

*Van der Loos et al. (2023) “Bone Mineral Density in Transgender Adolescents Treated With Puberty Suppression and Subsequent Gender-Affirming Hormones”. This looked at people average age 28, who had been on affirming hormones for an average of 11-12 years, having started affirming hormones at 16, after previously being on puberty blockers from tanner 2-3. Trans girls had lower bone mass than cis boys before the start of puberty blocker treatment. The study provided evidence that bone mineral accrual is temporarily suspended by the use of puberty suppression but, due to an increase during GAH treatment, BMD catches up with pretreatment levels at long-term follow-up, except for the lumbar spine in individuals assigned male at birth. The study concluded that treatment with a GnRH agonist followed by long-term gender-affirming hormones is safe regarding bone health in transgender persons receiving testosterone, but bone health in transgender persons receiving estrogen requires extra attention and further study.  Estrogen treatment should be optimized and lifestyle counseling provided to maximize bone development in individuals assigned male at birth. [Note this is yet another study inappropriately using Z scores compared to assigned sex which other lit (see earlier blog) has found are not the most useful way of studying bone density for this population]. Whilst this article predominantly compares trans people to the bone density of their assigned sex, when comparing trans people to their affirmed sex it notes “At follow-up, when participants were in their late 20s (around 28 years), the majority had z scores within the normal range when using reference data of the affirmed gender”.

Navabi et al. (2021) “Pubertal Suppression, Bone Mass, and Body Composition in Youth With Gender Dysphoria”. Found that reduced bone density of trans adolescents on puberty blockers was related to insufficient Vitamin D. Found that trans adolescents on puberty blockers need to take vitamin D. (This is standard healthcare). 

*Bachrach et al. (2023) “Bone Health Among Transgender Youth: What Is a Clinician to Do?” provides advice for clinicians on how to advise trans youth and families on managing bone health relating to puberty blockers.  

Articles related to research ethics on puberty blockers

*Ashley et al. (2023) “Randomized-controlled trials are methodologically inappropriate in adolescent transgender healthcare”. Outlines why RCTs are inappropriate, unpractical and unethical for puberty blockers.

*Moscati et al. (2023) “Trans* identity does not limit children’s capacity: Gillick competence applies to decisions concerning access to puberty blockers too!”. Outlines why being trans does not override important medical ethical principles of decision making.  

Articles related to height

Schulmeister et al. (2021) “Growth in transgender/gender-diverse youth in the first year of treatment with gonadotropin-releasing hormone agonists”. It looked at impact on rates of growth in height. It followed 55 trans adolescents who started blockers at average age 11, 62% at tanner 2 and 29% at tanner 3.  Pre-pubertal cis children grow at average 6.1 cm a year (range 4.3 – 6.5). Trans children who started puberty blockers at tanner II grew at a median of 5.3cm a year (range 4.1 – 5.6cm). Trans children who started puberty blockers at tanner III grew a median of 4.4cm a year (range 3.3 – 6.0cm). These rates are slightly lower rates of height growth than pre-pubertal youth. Trans children who started puberty blockers at tanner IV grew a median of 1.6cm a year (range 1.5 – 2.9cm), at a lower rate of height growth than pre-pubertal youth. In summary, trans adolescents on puberty blockers at tanner 2 and 3 continue to grow in height at similar rates to pre-pubertal children. Trans adolescents on puberty blockers at tanner 4 grow in height at slower rates. More information on the timing of affirmative healthcare and impacts on height will be valuable for those who desire a height in ranges typical for cis men and women.

*Boogers et al. (2023) “Transgender Girls Grow Tall: Adult Height Is Unaffected by GnRH Analogue and Estradiol Treatment”. This study looked at how gender affirming healthcare affects the height of trans girls. In the Dutch population, cis men reach a mean adult height of 183.8 cm, which is more than 13 cm taller than cis women (170.7 cm)  This study looked at 161 trans girls who started puberty blockers before age 16 and started oestrogen at an average age of 15 or 16 years old. The cohort were at different tanner stages when starting blockers (Tanner 2 – 5). The mean duration of puberty suppression 2.4 years. Individuals had an average growth velocity of 5.3 cm/year in the first year of treatment. This decreased to 3.5 cm/year in the second year.  When starting oestrogen at 15 or 16 they were either treated with estradiol at a regular dose (2 mg), with high growth-reductive doses of estradiol (6 mg) or with ethinyl estradiol (EE, 100-200 µg).

Growth velocity and bone maturation decreased during GnRHa, but increased during GAHT. Adult height after regular-dose treatment was 180.4 ± 5.6 cm.  Growth velocity in the first year of GAHT was 2.8 cm/year, which decreased to 1.4 cm/year in the second year. From the start of GAHT, height increased by 5.9 cm to an adult height of 180.4cm.

The high dose estradiol group mostly had 1.5 years on regular dose before moving to high dose. Compared to regular-dose treatment, this group reduced adult height by 0.9 cm (179.5cm).

The EE group reduced adult height by 3 cm (177.4cm). High-dose EE resulted in greater reduction of adult height than high-dose estradiol, but this needs to be weighed against possible adverse effects.

Individuals who started affirming hormones at a lower bone age reached an adult height that was 1.6 cm/year lower than those who started hormones at a higher bone age.

Potentially earlier initiation of estradiol in transgender girls (before age 15-16) might result in shorter adult height.

Willemsen et al. (2023) “Just as Tall on Testosterone; a Neutral to Positive Effect on Adult Height of GnRHa and Testosterone in Trans Boys”. This study looked at 146 transgender boys treated with GnRH analogues and testosterone who reached adult height. Adult height was on average 172.0cm. Trans boys who started pubertal suppression at a young bone age were significantly taller. PS and GAHT do not have a negative impact on adult height in transgender boys and might even lead to a slightly taller adult height, especially in those who start at a younger age.

*Ciancia et al. (2023) “Early puberty suppression and gender-affirming hormones do not alter final height in transgender adolescents”. This study found that trans boys and trans girls height aligned with cis peers of their assigned gender rather than affirmed gender, with puberty suppression and gender affirming hormones not impacting on height. This study was for trans boys starting puberty suppression at average age 12, and trans girls starting puberty suppression at average age 13 (I couldn’t see the age of starting affirming hormones as I can’t access the full article).

Science does not stand still. We need to ensure we are up to date with the latest research in this field. Charities and those supporting trans children and young people need to keep informed about the latest evidence, and ensure the most accurate, up to date, and comprehensive evidence is made widely available, for informed decision making.

Is this an abusive relationship?

(or why I won’t be responding to another government consultation on trans healthcare).

Just weeks after having submitted an invited response (invited as an academic expert) to a government consultation on making a legal ban on puberty blockers permanent, ANOTHER government consultation on trans healthcare has today been launched.

This one is on adult trans healthcare services. There are many reasons to approach this consultation with concern. The consultation itself provides a link to the incredibly biased and prejudice-ladden letter from Dr Cass which is a driver of this current review.

I cannot even remember how many government consultations related to trans rights or trans healthcare I have completed over the past 8 years. It is far far far beyond a joke.

And each public consultation takes the same form. The new NHS adults services consultation even provides a link to an analysis and summary of responses to the 2017 consultation. Reading the executive summary of that analysis is very telling and illustrative of the problem. In the 2017 consultation, responses were divided into three groupings:

  • Current, former or prospective user of gender identity services (30.15% of respondents)
  • Individual member of the public (26.8% of respondents)
  • Clinician (16.75% of respondents)

The 2017 consultation responses summarises very succinctly the differences between these responses (worth reading on pages 2-6). In short, the current and former users of gender identity services provided detailed and meaningful suggestions on how services could be reformed and improved. Clinician respondents, who were, mostly GPs, broadly didn’t know what to do with trans people and didn’t want to have responsibility. Members of the public felt being trans was a mental disorder and wanted services to be made significantly worse for trans people. The consultation presented all of these contrasting views, with the views of actual trans people in one grouping (glossing over nuances in actual recommendations re different ways of improving trans health), while views that were ambivalent or fundamentally opposed to trans well-being and healthcare rights were given equal weighting to those of actual service users.

This pattern has then repeated time and time again since 2017.

This pattern will be repeated in this new NHS consultation. Although now the anti-trans lobby is much more organised and assertive, so I expect even more volume of anti-trans submission, including from transphobic clinicians and medical professionals, and including from those purporting to be prospective service users (or concerned family members of service users).

This pattern of public consultation for minoritized healthcare is extremely abusive.

Every consultation response is a huge amount of effort to do well. It is a significant extraction of labour from already exhausted trans people, including from those of us who are called to respond as trans-supportive researchers or on behalf of civil society.

It is abusive to ask us for consultation after consultation after consultation. Every single one we respond defensively, knowing that the purpose of the consultation is not to improve services and respect rights, but to justify an ever further roll back of those rights, and ever more severe degredation of those services.

It is abusive to ask trans folks to engage in yet another consultation where the views of those fundamentally bigoted about trans existence are given equal weight.

It is abusive full stop.

This particular consultation is where I personally draw a line. It is not acceptable.

I expect adults trans healthcare will be made worse in the coming years, building upon Cass. I expect this public consultation, including the thousands of responses from profoundly anti-trans individuals and lobby groups, will be used to justify that degregation of essential healthcare. To justify the inclusion of ever greater rights violations in our healthcare. To justify ever greater encroach into the reasons to deny care to those of us who are the wrong kind of trans.

Esteemed trans healthcare scholar Dr Ruth Pearce wrote all the way back in 2018 (about another consultation on trans health conducted about us yet without us), that “we respond not with hope or optimism, but in fear. This is the power you wield over us”.

Over the past years I have responded to more government consultations on trans topics than I can count. Every single submission I have written, not out of hope, but out of fear. Out of a feeling of responsibility to use my relative privilege to at least try and change the outcomes, to raise my voice to highlight the current injustices and the harms of abusive practice.

But we are clearly not being listened to. Time and time again we are not being listened to.

How long do we keep collaborating in the same pattern. How long do we keep gas-lighting ourselves?

Today I’m saying no.

I refuse to remain in any part of this extremely abusive relationship.

I refuse out of principle to engage in any way with a consultation that is equally interested in the views of non-service users, that does not have really basic ethical commitments to trans depathologisation, dignity and healthcare rights, that does not have trans leadership and trans power at its centre.

I refuse to respond defensively while having zero hope that my words and my time are going to change the outcome. In this case, as before, I fundamentally don’t believe my inputs will in any way change the outcome. Quite the opposite – I believe my words and my submission, alongside those of others submitted and hard-worked-on out of a feeling of responsibility to our communities, will provide the government/NHS with a veneer of respectability, that they asked and listened to all views.

Listening to all views is not good enough. I literally cannot stomach another consultation that will be written up as “here’s what trans people want, however here’s what doctors and members of the public want, so we are therefore going to make trans healthcare worse”. It is not good enough. I am out.

I’m not saying that stepping out of this consultation will be enough to change the outcome. I’m not saying there is a clear path to trans justice.

But I’m at least not going to waste my time on another heartless and fundamentally flawed process.

Today I will choose to do something better with my time.

I hope we can at some point be more coordinated and demanding, standing together in solidarity and power, saying we will not engage with processes that are fundamentally dehumanising and abusive. Most folks I know right now are too worn down by all the loses, by all the pain, by all the energy expended on heartless consultations, to have the energy and reserves to try and take back any power.

Maybe that is one of the ways forward. For now we take time, we rest, we refuse to respond defensively, we let go of the fleeting hope that our submission will be enough to change power structures that continue to inflict harm after harm.

We focus our time and energy on ways to keep ourselves and those who are suffering afloat through these tough times.

We state clearly and in unison that when the government and the NHS decide they believe in our humanity, when they have an ounce of care for justice and equality, when they recognise that anti-trans views are not welcome in consultations on our healthcare, then we have plenty of ideas to share on the meaningful reform of trans healthcare. But until that approach is made in good faith, and with trans people in positions of authority – we have better things to focus on. We focus on surviving the anti-trans hate that continues to grow in the UK, including in senior leadership in the government and NHS.

.

WPATH 2024: Part Two

On the 3rd full day of WPATH 2024, there was one session that I wanted to write up in slightly more detail, as it is very relevant to those working with or supporting trans children and young people. (My original WPATH 2024 blog is available here). The session was titled “New long-term research on adolescent gender-affirming medical care”, with 5 presenters, three from the US, and two from the Netherlands.

I wanted to share my notes on these presentations here. First a big caveat – my notes and interpretation may not be 100% correct, I have not confirmed this post with the presenters of these studies, and these studies have not yet been finalised, peer reviewed or published. Therefore, the data in this study may change before acceptance into the formal literature. At WPATH, within the trans room, there was a discussion on the challenges of knowledge that is of vital importance to trans communities and families of trans kids being paywalled behind expensive and hard to attend conferences. Recognising the very slow timelines of academic publishing, there was a discussion on a duty to share early preliminary results not only with the clinicians and researchers who are able to attend WPATH, but also with the very interested and directly affected trans and family of trans kids communities, currently trying to defend our healthcare from attack, for whom new research is most important. In the trans room at WPATH we talked about our responsibility and duty of care as trans researchers with half a foot in clinical spaces to share information with those who cannot access. As part of this commitment I’m writing this blog.  

First Dr Diane Chen (she/her) presented on trajectories for mental health in the four years following gender affirming hormone initiation. She highlighted the six existing studies that examine psycho-social outcomes in US-based trans youth receiving oestrogen or testosterone (Allen; Achille; Kuper; Tordoff; Chelliah; Chen). These studies have generally found that aspects of mental health improve following initiation of gender affirming hormones. These studies have limitations including that they only follow youth for average of one year after treatment initiation, that they only focus on (internalising) areas like anxiety or depression, and the one article (by the presenter Chen et al) that looked at individual trajectories found significant individual variation around the average change in outcomes. For that study the presenter showed graphs showing, on average, a steep improvement in appearance congruence, a shallow reduction in depression and anxiety, and a shallow improvement in positive-affect and life satisfaction over 2 years. The individual dots show significant variability, suggesting a focus on the average experience may hide difference trajectories between sub-groups. The new study being presented here aims to look at potential distinct trajectories between sub-groups.

The new study (by Chen et al, not yet published), looked at data for 217 youth, average age 16 (range 11-20), 60% trans-masc, 34% trans-femme, 4% non-binary, 80% socially transitioned at baseline, 7.6% received gender affirming care in early puberty (defined as puberty blockers at tanner 2 or 3 or HRT at tanner 3). The study looked at internalising data on (anxiety/depression), at externalising (aggression, risk taking), experiences of gender minority stress, and parental acceptance. Data were collected at baseline, year 1, year 2, year 3 and year 4 [They applied latent growth curve modelling / growth mixture modelling for statistical analysis]. They presented graphs distinguishing three sub-groups that follow distinct pathways across the 4 years. 25% of trans youth in their study were identified as a ‘consistently low’ group who had low levels of anxiety/depression/risk-taking behaviours at baseline who continued to have low levels of anxiety/depression/risk-taking behaviours. 56% were classified as having ‘declining’ levels of anxiety/depression and consistently low levels of risk-taking behaviours, with levels of anxiety and depression slightly above a clinical diagnosis at baseline, later declining to slightly below clinical thresholds. 18% were categorised as elevated, having persistently high levels of anxiety/depression/risk-taking behaviours at baseline and later in study.

From further data analysis they discovered:

95% of youth who accessed early affirmative care were in the categories of consistently low (53%) and ‘declining’ levels of mental health problems, with only 5% of these youth in the category of having persistently high levels of anxiety/depression/risk-taking behaviours.

[Talking about ‘low’ and ‘declining’ as positive descriptors in a study on mental health at times feels a little counter intuitive, given we think of high mental health, or improving mental health as a good thing, whereas here we want to see low and declining mental health problems).

The youth who had consistently good mental health, or improving mental health had the following characteristics in common:

Less loneliness

Less gender minority stress

Higher parental acceptance

Higher emotional support

The study highlights that provision of HRT is not a magic cure to the mental health challenges of trans youth who are isolated, unsupported and facing anti-trans hostility and gender minority stress inside and outside of their homes.

Among youth with high levels of anxiety/depression/risk-taking behaviours at baseline, those with higher levels of baseline parental support were more likely to see improvements in their mental health.

Protection from gender minority stress, reduced isolation, emotional and social support, and parental support are all protective factors for trans youth mental health.

18% of the sample continued to have high levels of anxiety/depression/risk-taking behaviours throughout the study and this portion of trans youth would benefit from more targeted mental health support as well as support to reduce gender minority stress and isolation.

Next Dr Laura Kuper (they/them) presented preliminary findings of 5 – 8 year outcomes of the trans youth longitudinal survey. The study began in 2014 including annual youth and parent report surveys. It looked at quality of life, anxiety, depression, body dissatisfaction. Recently added new measures of gender dysphoria, socio-political stress and decision regret scale.

Wider study now includes 738 youth. At baseline ages 6-18 (mean 15), 64% assigned female at birth, 34% assigned male at birth. A few youth are now in year 9 of the study, most are currently in years 2-7 of the study (new enrolments to the study are being added each year).

Presented data on 267 youth and 317 parents who completed survey on access to treatment. The study looked at those who had started and at some point stopped treatment with oestrogen or testosterone. [For this presentation exact numbers were not provided and the graphs were hard to read precisely so there is a likely margin of error in the percentages I’ve given below – you’ll need to wait for publication of the proper research for the accurate numbers]

10% of those who had ever started oestrogen had at some point stopped oestrogen. The reasons for stopping oestrogen were examined. 1 was because was satisfied with the changes and didn’t need further oestrogen; 2 experienced unwanted changes; 2 had a change in their experience or understanding of gender; 2 stopped due to difficulties accessing oestrogen; 1 for other reasons. Just under half who ever stopped taking oestrogen ended up re-starting taking oestrogen. Youth and parents were asked the question re starting taking oestrogen “It was the right decision”. Around 70% of youth strongly agreed, 5% agreed, 2% neither agreed nor disagreed, 2% strongly disagreed. 60% of parents strongly agreed, 20% agreed, 2% neither agreed nor disagreed, 2% strongly disagreed. Youth and parents were asked the question re starting taking oestrogen “I regret the choice that was made”, and “the choice did me/my child a lot of harm” with the same findings (vast majority strongly disagreed, with only around 2% strongly agreeing).

32% of those who had ever started testosterone had at some point stopped testosterone, significantly higher than the portion who ever stopped oestrogen. The reasons for stopping testosterone were examined. 16 were because were satisfied with the changes and didn’t need further testosterone; 8 experienced unwanted changes; 8 had a change in their experience or understanding of gender; 2 had legal barriers to access; 23 (the largest portion) stopped due to difficulties accessing testosterone; 19 for other reasons. Just under half who ever stopped taking testosterone ended up re-starting taking testosterone, with several going through multiple points of stopping and re-starting. Youth and parents were asked the question re starting taking testosterone “It was the right decision”. Around 154 of youth strongly agreed, 8 agreed, 2 neither agreed nor disagreed, 1 (hard to read graph) disagreed, 1 (hard to read graph) strongly disagreed. 145 parents strongly agreed, 32 agreed, 7 neither agreed nor disagreed, 2 disagreed, 3 or 4 (hard to read graph) strongly disagreed. Youth and parents were asked the question re starting taking testosterone “I regret the choice that was made”, and “the choice did me/my child a lot of harm” with the same findings (vast majority strongly disagreed, with only around 1% strongly agreeing).

Dr Kuper then moved on to present findings on a 5 year longitudinal study of trans youth receiving oestrogen or testosterone. The study currently includes data for 558 youth at baseline, 431 at year one follow up, 275 at year two follow up, 163 at year three, 115 at year 4, 59 at year 5. The declining numbers at later years of follow up is because new youth keep being recruited into the study (not linked to drop out). [They applied linear mixed effect modelling to the dataset for statistical analysis].

Graphs were presented showing a significant and steady decrease in body dissatisfaction over 5 years time for both those on oestrogen and those on testosterone (with the same pattern for both). A graph of depressive symptoms showed a steady decrease in depression scores over the 5 years. The slope and change in depression was similar for both those on oestrogen and those on testosterone, but with those on testosterone having slightly higher depression at baseline and at current measure than those on oestrogen. Both groups were over the point for mild depression and near the level for moderate depression at baseline, and fell to at or just over the point for mild depression at current measure. Graphs showed some improvements in anxiety over time. Quality of life scores improved steadily over time for both groups.

Overall conclusions were:

Strong satisfaction with decision to receive treatment from youth and parents

Large improvements in body dissatisfaction, seen as the primary goal of treatment

Modest improvements in mental health and quality of life, which were also impacted by gender minority stress. They noted that this sample is in Texas where there are very significant socio-political stressors and state persecution, which is likely impacting on mental health measures.

This research also underscores the unsuitability of having mental health improvements as a key justifier for gender affirmative healthcare – especially for those youth who (through social support) have low levels of mental health at the start of puberty. Those youth do not see improvements in mental health, they see their good levels of mental health retained through medical transition. Reviews like the Cass review critiqued affirmative healthcare for not showing puberty blockers not having a significant enough boost to mental health – this is clearly the wrong variable to be tracking.   

Next Dr Kristina Olson presented on trans youth satisfaction with care. She presented existing knowledge on youth satisfaction with care, including the high levels of continuity of care, with the assumption that trans youth would not continue to take active efforts to continue healthcare that they did not want to continue. Also low rates of detransition to live as cis amongst trans youth who commence gender affirming healthcare. We also know there are cases of detransition / dissatisfaction, whilst noting that these two concepts are different and distinct.

This new study aimed to assess levels of satisfaction and regret following puberty blockers and HRT, and to assess continuity of care. Looked at trans youth project, more than 300 socially transitioned binary trans youth recruited between ages of 3 and 12 in years 2013-2017. Mostly US trans youth with some Canadians. Youth followed up every 1-2 years. Study has now been ongoing for 7 – 11 years. Youth have answered questions on average 3.8 times, and parents have answered questions on average 5.8 times. This study presents data from 2023 questionnaires, given to all youth who are currently 12+ and to one parent.

On average the cohort had socially transitioned at 6-7 years old. On average they had started blockers 5 years before the survey, at 11 years old. On average they had begun HRT 3.5 years before the survey, at 13 years old. This cohort, supported in childhood, has had good levels of mental health throughout childhood and into adolescence, with slightly elevated anxiety, matching well-being of cisgender peers.

269 were aged 12+ and had started gender affirming medical care and were eligible for this survey. 220 or 82% completed the survey. For the 18% who did not fill in this specific survey, the research team do have continuity of care medical records. Where data is provided by a youth and their parent, the data tables only show the youth report. Where youth data is not available, the parent reported data is provided.

215 reported on their experience with puberty blockers (160 direct from youth and 55 from parental report). Satisfaction was rated from 1 not at all happy to 7 extremely happy. Satisfaction was rated 6.4 average for youth and 6.7 average from parents. Regret was rated from 1 no regret to 7 strong regret. Regret was 1.5 for youth and 1.3 for parents.

170 reported on their experience with oestrogen or testosteone (119 direct from youth and 51 from parental report). Satisfaction was rated 6.5 average for youth and 6.9 average from parents. Regret was 1.4 for youth and 1.0 for parents.

Very high levels of satisfaction and very low levels of regret

Also asked participants if they would have preferred to receive healthcare treatment at a different time, with options: ‘wish earlier’, ‘correct age’, ‘wish later’, ‘wish never’. 2% of youth wished never to have received puberty blockers, 2% wished to have never received hormones, 1 parent in the sample wished never to have received puberty blockers. 18% of youth (4% parents) wished they had received puberty blockers earlier and 74% youth (86% parents) felt they had received them at the right time (in a sample receiving puberty blockers at average age 11). 34% of youth (19% parents) wished they had received oestrogen or testosterone earlier and 53% youth (75% parents) felt they had received them at the right time (in a sample starting oestrogen or testosterone at average age 13 years old.

From the overall sample, 97% have continued to access gender affirming medical care to this day. 2% have stopped accessing gender affirming medical care.

Overall – very high levels of satisfaction, very low rates of regret,

Only 9 individuals out of 220 sample (4%) experienced regret. 8 (3.6%) experienced regret for blockers, 3 (1%) experienced regret for hormones. From these 9 2 individuals (1%) expressed regret for both blockers and hormones. 4 of the nine stopped all treatment, 1 in the process of stopping treatment, 4 have continued to take blockers or hormones. From the nine expressing regret, about half regret ever starting treatment, about half regret a specific side effect or complication or regret not skipping straight to hormones without time on just blocker.

A majority of youth continue to express high satisfaction with care many years later. This cohort seems to align closely with their cisgender peers on mental health, well-being, and on rates of change of gender identity. Important to note that the access to gender affirming medical care that has accompanied this cohort, is harder to access today for their younger peers, with increasing barriers to trans healthcare across and beyond the USA.

Next Dr Marijn Arnoldussen from the Netherlands. The presentation was titled “gender related and psychological outcomes in adulthood after early gender related medical transition in adolescence”. Studies from the Netherlands tend be of interest, because they were an early supporter of a limited form of gender affirming care, with puberty blockers prescribed to a 13 year old trans boy starting in 1988, and with decades of follow up studies. Studies from the Netherlands also come with some significant baggage, in a highly controlled and potentially pathologizing and psychologically invasive model of care, where folks were expected to conform to a very defined stereotype of trans-ness to receive care. The narrowness of the model of expected transness has relevance to some of their outcomes. Knowing the UK children’s GIDS model sought to replicate the Dutch model, and knowing very closely just how abusive, invasive and harmful the UK approach to trans children has been, makes me approach data from the Dutch clinic with a significant degree of concern, especially where clinicians report data without asking centring the views of their patients, or where clinical control, coercion and pathologisation is apparent.

 The study aim was to describe long term gender outcomes, treatment regret, reflections on gender related medical care, and psychological outcomes for trans adults who received gender affirming medical care, including puberty blockers, during adolescence. The study focused on trans adults who took puberty blockers during adolescence and who started gender affirming hormones over 9 years ago. 145 service users were eligible, of whom 72 participated. This is clearly a pretty high drop out rate. In the UK service, high drop out rates are sometimes an indication of service users not having confidence in clinical research.

From the 72 participants, 51 (71%) were transgender men, 20 (28%) were transgender women. 1 (1%) non-binary. The binary focus of the cohort is perhaps unsurprising if, as was certainly the case in UK children’s clinics, non-binary transitions were not supported or permitted. Interesting that this  cohort who started medical transition in adolescence a decade ago, has significantly more trans men than trans women – when this phenomenon is noted in current youth it is blamed on tiktok which clearly did not exist a decade ago. This cohort started puberty blockers at an average age of 14.85 (range 11.47-17.97) and hormones at an average of 16.67 (range 13.93-18.46) and are followed up at average age 29.1 (range 25-36.29 year old). The oldest in this cohort are 36 years old. Hardly new treatment.  

94.4% had not experienced any change in their gender identity over time from starting blockers at  average age 14 to now being on average 29 years old.

83% (60 people) had not experienced any regret or doubt about their gender affirming medical.

17% (12 people) had experienced some form of doubt or regret – however:

For 2 people (3%) this was occasional thoughts what their life would be like if they hadn’t had medical transition, doubts rather than regrets.

3 people (4%) regretted the chosen surgical technique in genital surgery

4 people (5.6%) regretted either genital surgery or surgery to remove reproductive organs. This figure in particular need to be considered against two important realities – one, stating a desire for ‘full’ transition was in many places considered a key eligibility criteria for any form of medical transition, closing down possibilities for a less binary transition pathway, and two in the Netherlands until very recently surgical transition was deemed necessary for eligibility to change your legal gender and to access various state protections or rights as a trans person. I would assume that where there is pressure to engage in surgical transition, incidents of regret is arguably more likely.

2 people (2.8%) regretted becoming infertile and being unable to preserve sex cells

1 person regretted the hormones and surgery they received.

From the 72 patients followed into average age 29, only one stated a regret of hormones.

The cohort were asked about their ability to make decisions in adolescence. A significant majority, 50 people (69.4%) felt they were capable to make decisions at an even younger age then they were permitted to do under the Dutch model (where they received blockers at average age 14 and hormones at average age 16). 17 people (23.6%) felt they were at the right age for their decisions. 5 people (6.9%) felt they were too young, with these people particularly mentioning the impact on their fertility.

Overall, 98.6% of people were satisfied with their social and medical transition overall. 15% had some doubts or regrets, with this particularly related to aspects of surgical transition. 1 person regretted hormones and surgery. 93% felt, on reflection, they were capable to take decisions on medical transition during adolescence.

Finally in this session there was a presentation from Dr van der Meulen from the Netherlands entitled “sexual dysfunction after early endocrine treatment: long-term study in transgender adults”.

This session had elements of exoticisation and pathologisation of trans people that I found uncomfortable. I’ll share some of the results here. A study on 70 trans adults, comparing those who medically transitioned in early puberty (tanner 2 or 3) with those who medically transitioned in later puberty (tanner 4+). They were average age 29 during this research. For the 50 trans masculine participants, 18% medically transitioned in early puberty, for the 20 trans feminine participants 40% transitioned in early puberty.  

Amongst the groups of adult participants (average age 29), they were asked about experiences of sexual disfunction. For trans men 18% reported a problem with low sexual desire (80% reported no problem with sexual desire), and low sexual desire was reported for 22% of those who transitioned in early puberty compared to 17% for those who transitioned in late puberty. 16% of trans men reported too much sexual desire (64% reported no problem with too much sexual desire) and too much sexual desire was reported for 11% of those who transitioned in early puberty compared to 17% for those who transitioned in late puberty. 4% of trans men reported low sexual arousal (96% reported no problem with sexual arousal) and low sexual arousal was reported for 11% of those who transitioned in early puberty compared to 2% for those who transitioned in late puberty.; 24% reported difficulty orgasm (74% reported no problem orgasm) and difficulty to orgasm was reported for 33% of those who transitioned in early puberty compared to 22% for those who transitioned in late puberty.

For trans women 20% reported a problem with low sexual desire (60% reported no problem with sexual desire), and low sexual desire was reported for 38% of those who transitioned in early puberty compared to 33% for those who transitioned in late puberty. 0% of trans women reported too much sexual desire (100% reported no problem with too much sexual desire). 20% of trans women reported a problem with low sexual arousal (65% reported no problem with sexual arousal) and low sexual arousal was reported for 0% of those who transitioned in early puberty compared to 33% for those who transitioned in late puberty.; 35% reported difficulty orgasm (65% reported no problem orgasm) and difficulty to orgasm was reported for 0% of those who transitioned in early puberty compared to 58% for those who transitioned in late puberty.

Overall sexual disfunction was relatively low amongst these trans adults who medically transitioned in adolescence. There was no significant difference in sexual disfunction between those who medically transition in early puberty compared to those who sexually transition in late puberty. [Research on this topic surely, SURELY needs to better centre the voices and priorities of trans adults, and the multiple factors beyond early or late medical transition that likely impact on experiences – and surely some comparison to cis people’s experiences of sexual disfunction would make such research somewhat less exoticising and othering…]

A few follow up questions were held. One questioner stressed the importance of timeliness of publication of all the above new data – especially in contexts where healthcare is under attack. Another questioner asked about the mental health of neurodivergent populations, asking if datasets could be considered to see where autistic youth fitted on the mental health trajectories, noting the greater mental health challenges and [Is there a term like gender minority stress that applies to the stresses of navigating a neurotypical world?] that are carried by autistic youth that will not be ameliorated by gender affirmative care. There was also some discussion on what outcome indicators are best to track to monitor the impacts of gender affirmative healthcare, with panelists commenting that a narrow focus on mental health is probably not the right indicator.

I didn’t share any of my own research this time at WPATH, but given the WPATH content was very significantly dominated by US and Dutch research, I’ll end by sharing my contributions to the literature on puberty blockers here:

“I Didn’t Want Him to Disappear” Parental Decision-Making on Access to Puberty Blockers for Trans Early Adolescents – available here.

Experiences of puberty and puberty blockers: Insights from trans children, trans adolescents, and their parents – available here.

WPATH 2024

At the end of 4 days of trans health presentations from researchers, clinicians and community advocates from across (parts of) the world, I wanted to capture some of my key learnings and reflections. The conference took place the last week of September, in Lisbon, Portugal. This is my first WPATH (a conference of the World Professional Association for Transgender Health). A majority of trans communities have no access to WPATH information, yet WPATH learning is important to many trans people and families. I’ve always appreciated those (especially Ruth Pearce) who try to make conference information available to those unable to attend. I note the significant barriers to attendance for those without an employer or institution to fund expensive attendance fees and travel, to those with disabilities or caring responsibilities unable to travel, for those without a visa to come to Europe, to those facing other barriers to attendance.

Overall vibe

The overall vibe was better than I had expected, although my expectations were drawn from hearing really poor experiences at past WPATH conferences. I found overall the tone of trans positivity, depathologisation, treating trans people as equals, centring research and healthcare ethics, was better than I had expected. However, there were still a portion of content and conversations where biases were clearly on display. I particularly noticed these biases in the very frequent exclusion of non-binary existence, on the continued pathologisation, mistreatment and exoticisation of trans children, and on a very significant domination of a US and white perspective, with notably limited representation from global majority populations. I gather only 3 attendees were from Africa (out of 1,445 registered in-person attendees). I also am scratching my head to think if there was even a solitary reference to the experiences of trans children in care in the presentations I attended – I don’t think there was.

The event had a trans chill out room where trans attendees could step away from the main event to decompress and reflect. It was noticeable that few trans attendees spent time there in the first days of the conference, with the fullness of the room growing over time, as trans researchers, clinicians and advocates encountered more challenging content and interactions. On the third day I heard one person reflect that despite WPATH improvements, it is noticeable just how many trans people are sat in the trans space burnt out by negative engagements by day three of four. I myself had a number of negative and hostile encounters, and a number of presentations that I could not sit through, finding some content taxing or upsetting, particularly where content demonstrated abusive clinical or research practices towards trans children. There were a number of other challenges at the conference, with no encouragement of sharing pronouns (apparently pronoun ribbons were lost in shipping), not being able to find gender neutral toilets on the first evening, and apparently some staff policing of toilet usage which was rather surprising in a trans health conference.

There were also a large number of encounters and presentations that were an absolute delight. I met a huge number of people from across different countries and disciplines who deeply care for improving equality and justice for trans people of all ages and situations. I heard some research that shows where we should be in terms of ensuring research and healthcare is centring the rights and needs of trans communities. One clear highlight was an opportunity to connect with TPATH, the trans professional association for transgender health, including an opportunity to connect with some Portuguese trans folks who were not able to attend the conference.

 Session structure

 The session included plenary speeches, symposia, oral abstracts and posters. I will write about each in turn.

Plenary sessions.

On each day there were two plenary sessions, that were hour long speeches to the full audience, from one or two speakers, with a moderator. The plenary speakers were appointed by the WPATH president. Three were related to surgery, which I won’t engage with here as its not an area I focus on or know a lot about. A broader reflection was that at times the plenaries overall were a source of pathologisation, erasure of non-binary people, dehumanisation, exoticisation, and demonstration of clinical control over trans communities. There were several sessions where, if one had a bingo card of common areas of biases and indicators of cis-supremacy, one might have ticked off many exemplars. The speakers also privileged a white, cis, US/European, abled, and clinical position. Of the plenary sessions, the one I enjoyed the most was the opening plenary, delivered capably by an American, the US state representative for Montana, Zooey Zephyr. It was a powerful and moving speech, capturing the challenges that we currently face. I particularly resonated by the words (that I am paraphrasing), that when anti-trans laws are passed, when communities face state persecution, the harm comes severe and fast, whilst processes to overturn such harms are drawn-out and slow. Those words certainly resonated with my experience in the UK, where the harms of recent criminalisation of adolescent healthcare has indeed been severe and fast. The speech and presentation was excellent, but very US centred for an opening plenary. I wouldn’t expect anything less than US centred content from a US state representative, so this US centring is more a question for WPATH leadership than for the presenter. Why would a WPATH opening plenary would be so US centred. The tendency for WPATH (the World association) to act as US-path on holiday does appear to continue to be on display. However, this opening plenary was at least very strongly trans-positive, centring trans rights, calling attention to the abuse, control and persecution of trans communities, including trans children. The other plenaries alas did not all maintain this important commitment on trans-positivity, rights and justice. Several centred a clinical perspective grounded in assumptions of clinician control over trans lives. The plenary on trans children was particularly problematic and disappointing, presenting to a wide audience some older concepts and research that are problematic and outdated, centring and justifying clinical control over trans children. There were times across the plenaries where trans community and service user voice and perspectives were absent, with speakers prioritising a cis, adult, white, global North, clinician perspective. 

I was disappointed to have the plenary on puberty blockers delivered by stakeholder from the Dutch clinics, whose model does not centre trans child and adolescent rights. The presentation itself summarised older research (some of which is problematic) and failed to update the audience on newer research findings from other countries. It was a really lost opportunity to update general attendees on the most up-to-date research on puberty blockers. I also wish we could hear more from Dutch trans communities and service users, particularly child service users, on the Dutch approach. My own research has centred the experiences of service users in the English Children’s Gender Service, which aimed to replicate the Dutch model. My own experience and my research with that service has demonstrated widespread clinical abuse and harms to trans children in that service. (My research, including on experiences in gender clinics, experiences of childhood social transition, experiences with puberty blockers, and on pathologisation and cis-supremacy in healthcare can all be found here).

I hope the next WPATH can better centre child rights, trans rights, an ethics of depathologisation and equality in future plenary sessions, ensuring that any presentations from clinicians centre some fairly basic ethical commitments.

Parallel sessions

Across the conference there were 14 different sessions (hour long time slots), during which attendees had to choose between 5 parallel options, 3 of which were usually symposia and 2 of which were oral abstract sessions. That meant there were a total of 70 hour long sessions, that we could attend only 14 of. The sessions we could attend are recorded and available to watch on catch-up, and I’ll certainly check in on some of the ones I missed in coming weeks. Here I’ll comment on some of the symposia of oral abstract sessions that I attended.

Symposia

On being a target

There was an excellent session on trans researchers being a target of hate and harassment. Unsurprisingly it featured two UK researchers, talking about the amount of targeted hate that comes with being a trans researcher in the UK. We need to find better ways of supporting trans researchers. And we need our institutions to step up, both to protect trans researchers from external abuse, and to ensure research spaces and universities are actually safe from organised transphobia.

Trauma-informed approaches to care

This session talked about trauma informed approaches. I’ve not heard much discussion of this before, and certainly not on how to ensure child and adolescent care is trauma informed. I noted particularly the discussion on how certain mindfulness techniques are inappropriate and triggering rather than relaxing for those living with trauma. I recognised this in myself (I find mindfulness unbearable), but wasn’t aware this was a more general phenomenon. There has been a big recent focus on mindfulness in schools in the UK, and I wonder how this is being experienced by children living with trauma, which will include a lot of trans children.

Evolution of gender expression care

This session focused on the support that trans people, and especially younger trans children, may benefit from in areas of their life not related to medical care. The presenters are including the term ‘gender expression’ care to capture support with social transition, gender expression and finding gender joy, as distinct from and running parallel to medical transition support.

New long-term research on adolescent gender-affirming medical care

This session was excellent, with three important presentations from the US, from Diane Chen, Laura Kuper and Kristina Olson. I will write up some more detail on these three presentations soon as they are very timely and relevant. This is now written up as a separate blog post here.

Preserving evidence-based trans healthcare for adolescents in Europe and North America

This included presentations on how clinicians are navigating care restrictions and challenges to care. It included a focus on the UK, USA, Croatia, as well as discussion on upcoming guidelines from Switzerland, Germany and Austria. It included discussions of clinical care on the defensive, and how to ensure services that are under attack are shifted to the most defensible positions. I would have liked a more significant focus on how to ensure ethical principles and child rights within services that are under attack. I would have liked more explicit discussion of the impacts on trans children of a shift into defensive practice, which often includes bringing in or maintaining approaches that are not in a child’s best interest. I would have liked more consideration of how to ensure child rights and prioritised while operating under defensive practice, and more explicit acknowledgement of the harms, and more proactive work to ameliorate such harms. I’d also like more discussion of how a shift to defensive practice can provide a cover for coercive and harmful practices beyond what might be 100% essential. And how those shifting to defensive practice need to be more rather than less accountable to criticism of their practices. We also need to consider whether shifting to the most defensible positions actually appeases or reduces criticism from trans-hostile actors – in the UK this was certainly not the case, every shift to the defensive led to more attacks on care. I think a ethical and rights based defense of care is stronger than any effort at appeasement. (This session clashed with another session on “Research-based, ethical, lifesaving: findings from a long-term satisfaction study on pediatric gender affirming care” that I hope to catch up on later.

Centring Gender Diverse Young Children’s Voices and Experiences in Clinical Care and Research

A tool developed by Zucker (1977) was presented, with discussion of its cisnormative flaws and failings. The presentation then talked about experience of modern research using this tool. I don’t understand using an outdated and inappropriate tool developed by Zucker with modern trans children. I didn’t stay for the full presentation so perhaps I misunderstood something. I worry about research practices that do not centre trans children’s well-being and do not protect from research related harms. In my experience every question asked to a trans child by a professional, of any type, is an example of that child being treated differently. Children notice when their identity is treated differently. They notice when they are being studied. All research needs to consider the potential for children feeling shame. I returned to the session later for a discussion on the use of dolls to help children display their gender. I was probably not in the best head space for the doll discussion. Again, I was prompted to ask myself how many cis children are asked to dress a doll in a meaningful outfit under adult stranger/professional scrutiny. How do those trans children feel. I’m sure this can be done in a really positive way, and I don’t doubt the researchers presenting who seemed lovely do this in a positive way. But there was also suggestion of sharing this approach and these dolls much more widely. I didn’t stay for the whole session. I hope there was also significant discussion on the many trans children who do not want to dress dolls while under adult scrutiny, on the children who don’t want to be treated differently just because they are trans. I hope there was discussion on the ways in which a doll dressing exercise can be done really badly by the wrong facilitator, how it could be experienced by a child as being a subject of adult curiousity of how different and weird they are compared to their siblings and peers who are not asked to do this task. I worry about any initiative that en masse treats trans children in a different way to cis children, and anything that is not individually determined and centred. The younger children who I have known most closely would have hated being asked to dress a doll to present themselves, especially at a point in time early in transition where their clothing and expression is being most extremely scrutinised and judged and commented on by those around them. For all of these tools, I guess the context and the intent is really important. In a really safe environment, where children are not already feeling hostility and judgement and shame, perhaps a doll dressing challenge could be a source of gender joy for some children. How do we know which environments are safe for this? How do we know which children will enjoy it? How do we offer this as one of very many, many, fun activities, and ensure children do not feel compelled to engage as part of defending their existence to the adults around them. Given the choice of a coordinated doll dressing activity and a game of tag or watching a movie, a majority of the trans kids I know best would choose tag or watching a movie. In my experience, younger trans children, especially those early in transition, are very very tuned in to any areas of their life where they are treated differently or scrutinised. How do we ensure that activities that treat them differently do not make them feel like there are being judged or assessed, or make them feel they need to perform to meet adult expectation or approval.

Oral abstracts

Engaging Family

There were several presentations on engaging with families. It is interesting to see the work that is being done with families who help them to better understand and support their trans children. One reflection that I had, was on how can support services better recognise a diversity of support needs amongst parents.

From my own experience I wonder about the targeting. In my experience the parents and carers who show up, who are reachable with interventions, are less likely to benefit from basic trans 101 education and support with things like ‘ambiguous loss’. As a trans person and a parent in such spaces, I have found some ‘support’ to be really upsetting, and I know plenty of cis parents who have felt the same – who have needed support in managing state oppression and the minority stress of being a family facing overt anti trans abuse and hate, who have found sessions focused on ambiguous loss or trans 101 a world away from the support that they actually need.

On the topic of ambiguous loss I also wonder how we can better recognise the way in which rhetorics of ambiguous loss provide some parents with a cushion that enables them to gain emotional support from trans-ignorant cis communities – for that parent, moving away from a rhetoric of ambiguous loss also means moving away from their available emotional support network. That support network needs to be replaced by a trans-positive support network, and I’d really be interested in seeing how support for parents can focus less on trans 101 or on dealing with ambiguous loss, and more on building trans positive emotional support networks, reducing the isolation of supportive parents/carers, and on providing meaningful support to help families facing state persecution, helping parent/carers emotionally stay afloat whilst engaging in constant advocacy for child rights and whilst facing harassment, isolation and abuse.

Especially in context where oppression is high and rising, I would love to see more focus on how to ensure supportive parents and carers can not fall apart under the strain. Of course, the trans-hostile and trans ignorant parents are also very important – I would just not assume that they are the parents who will voluntarily walk through the door. Unless you have other means of reaching such parents (eg direct referral from the GP, or targeted outreach with a less supportive parent building on a connection with a more supportive parent), I wouldn’t assume you are ever meeting those parents.     

I would also like to see more consideration within those facilitating and organising parent/carer support groups of how to ensure the spaces do not expose parents/carers to an excessive amount of anti-trans opinion. In my experience those spaces work best when they are a good mix of parents who have become strongly supportive and educated, who are actively fighting for trans children’s rights and those parents who are new and managing their own learning curve. I have noted a tendency for the facilitation of these spaces to have shifted towards younger, non-parent and trans facilitators. I have also noted a growth in space for parents to discuss at length their own transphobic assumptions, where facilitators perhaps want every parent to have their say and don’t feel able to police any minimum standards of respect. The last ‘support’ group I attended I was directly called a ‘traitor to feminism’ for being a non-binary person in a facilitated group discussion without any backup.

(as well as being a toxic work environment for a younger trans facilitator) this ‘let everyone speak their mind’ approach is also driving away those parents who are more supportive. The cis parents who are attending in search of a safe space away from a trans-hostile world are encountering yet more trans hostility in those facilitated support spaces, and many are stopping attending. I myself more often than not find such spaces traumatising rather than reinvigorating, and I know many cis parents who feel the same. If the more supportive parents, who are looking for support on trans advocacy and dealing with transphobia get deterred from support groups, then that is a huge loss to those new parents who usually learn a lot of trans positivity and how to better support their children from parents who have walked the same path. I would be interested to hear more research that recognises the diversity of positionality within parents groups (including the existence of trans parents in those spaces), how to ensure those spaces are overall safe spaces for all parents (whilst providing some space for parents sharing their worries), and a mechanisms for more targeted approaches where a trans 101 isn’t the starting point for all families, with an emphasis on the support required beyond trans 101.

I always find the topic of ‘ambiguous loss’ a bit triggering. Clearly some parents do experience it, and need some therapeutic support with it. I wish there was more recognition of the diversity of ambiguous loss. In my experience a majority of parents experience ambiguous loss, which when you dig deeper is about a loss of safety. Especially for white families in countries and areas not particularly affected by violence or conflict, parents have an expectation of safety for their child. When they realise their child is trans, parents can have a reaction of fear, that their child is not going to be safe, in the present or in the future. This loss of expected safety is something that parents can find emotionally upsetting. In a world where there isn’t much language, parents can fall to a language of ‘grief’ to explain this loss. For some parents who I know, the language of grief is a mis-application, describing something that is different to grief. I’d like to see more focus on loss of safety as a concept, including helping parents to re-examine and re-conceptualise what they are feeling, especially where their feelings are not really about grief.

Clearly some parents also feel something like grief. One presenter mentioned an initiative on creative writing to help parents process their emotions. They included a description of a parent writing a eulogy. I am not a counsellor and don’t know how best to help parents who feel that way. I do worry about how much acceptance or space we should give for a grief narrative in more general or plenary spaces. It is clearly offensive. I also worry about the impact of giving space to a grief narrative on those parents and carers who have actually lost a child. Parent support spaces should be a safe space for those parents too, and I think more care should be taken over how ‘ambiguous loss’ is dealt with, including ensuring there are spaces for parents who want to talk about a loss of safety without having to hear other parents talk about ‘grief’ for a still alive child.

Law, Policy and Ethics

This included a presentation on the reasons why a proposed NHS research trial on puberty blockers is unethical, as well as evidence on the negative impacts of US healthcare bans.

Community engagement

This was a fantastic session, centring trans led research including from India, centring trans-led community designed research, the roles of community initiatives in steering research or clinical practice, and the importance of gaining service user trust.

Other conversations

I had many other interesting conversations. In many countries it was shocking to me to hear just how very far ahead of the UK in terms of treatment and support for trans children and adolescents they are. Folks from many countries expressed concern and solidarity on just how bad the UK is right now, seeing it as so very far behind acceptable levels of care, law and policy. I heard about interesting upcoming work, about current practice in the US, Canada, Australia, New Zealand, about support for trans youth in countries like South Africa and Vietnam, about upcoming research on disassociation, about initiatives to support folks under state violence. I met many awesome people who I hope to stay in touch with.

Gender Dysphoria and puberty blockers

In trans children’s healthcare there is so much intentionally bad science, so much science that fundamentally misunderstands (or chooses to misrepresent) trans experiences.

The quantity of bad science overwhelms – we challenge some, whilst other pieces of bad science slip through undetected.

I just this morning had my attention drawn to some fundamentally bad science (I read about it on the website transfemscience https://transfemscience.org/articles/puberty-blockers/ ) and realised that yet another bad faith move had somehow escaped my attention.

The Cass Review makes the claim that puberty blockers don’t reduce ‘Gender Dysphoria’. In recent discussions on this topic I have argued that this is likely both true and irrelevant. Puberty blockers shouldn’t be expected to reduce gender dysphoria, they don’t magically make trans kids feel better about their primary sexual characteristics. Instead they prevent the increase in gender dysphoria that can occur at puberty, if adolescents denied blockers are forced through the distressing development of unwanted secondary sexual characteristics. I have argued, including in recent media interviews, that puberty blockers shouldn’t be expected to reduce dysphoria, instead they prevent an increase in dysphoria at puberty.

HOWEVER. The term gender dysphoria has multiple meanings. One meaning refers to ‘physical gender dysphoria’, how we feel about our bodies, and particularly how we feel about the parts of our bodies that are impacted by sex hormones. A second meaning refers to ‘social gender dysphoria’, relating to our experiences navigating the world, including how we feel when we are mis-seen and misgendered. A third meaning references the diagnosis of ‘gender dysphoria’ from the Diagnostic and Statistical Manual of Mental Disorders, which has distinct definitions for children or for adolescents and adults, which operates as a proxy for a medical diagnosis of being trans.

In healthcare research a research question that is arguably valid and good faith is ‘does affirmative healthcare reduce physical and social gender dysphoria’. Asking this question about puberty blockers alone would be mis-placed (an error I thought the Cass Review was making) because puberty blockers don’t reduce physical and social dysphoria, they prevent it from getting worse.

However, this isn’t what they are talking about at all,

Let’s take a 2021 UK GIDS (NHS children’s gender clinic) research article on puberty blockers as an example (GIDS research has tended to be so filled with flaws, methodological, analytical, ethical and interpretive, that it is exhausting to read or critique, which is one reason the flaw highlighted in this blog has escaped me until today).

The 2021 article is titled: Short-term outcomes of pubertal suppression in a selected cohort of 12 to 15 year old young people with persistent gender dysphoria in the UK

The article talks about the purpose of blockers “used from early/middle puberty with the aim of delaying irreversible and unwanted pubertal body changes”. So we are talking about physical and social gender dysphoria, right? I’m pretty sure we’re not talking about identity…

The paper talks about measuring the intensity of Gender dysphoria. “The Utrecht Gender Dysphoria Scale (UGDS) is a self-report measure used to assess the intensity of GD validated for age 12+”. This is the only information on gender dysphoria provided in the article. If you don’t already know the Utrecht scale, you are left in the dark on what is being meant and measured here.

The article concludes that “Gender dysphoria changed little across the study”. Again, a finding that intuitively sounds predictable for physical and social gender dysphoria. I would expect them to remain the same (rather than worsen) if accessing puberty blockers. The idea we are talking about physical dysphoria appears to be reinforced by the next sentence “This is consistent with some previous reports and was anticipated, given that GnRHa does not change the body in the desired direction, but only temporarily prevents further masculinization or feminization”.

The article is not clear what is meant by gender dysphoria, and it includes several references to puberty blockers preventing secondary sex characteristics, so I do not blame past me for assuming we were talking about physical gender dysphoria.

BUT – then I went and looked at the measurement tool being used. The Utrecht gender dysphoria scale.

This is a simplified version of the Utrecht scale. It shows the measures that puberty blockers are being criticised for failing to improve:

1. I prefer to behave like my affirmed gender.
2. Every time someone treats me like my assigned sex I feel hurt.
3. It feels good to live as my affirmed gender.
4. I always want to be treated like my affirmed gender.
5. A life in my affirmed gender is more attractive for me than a life in my assigned sex.
6. I feel unhappy when I have to behave like my assigned sex.
7. It is uncomfortable to be sexual in my assigned sex.
8. Puberty felt like a betrayal.
9. Physical sexual development was stressful.
10. I wish I had been born as my affirmed gender.
11. The bodily functions of my assigned sex are distressing for me (i.e. erection, menstruation).
12. My life would be meaningless if I would have to live as my assigned sex.
13. I feel hopeless if I have to stay in my assigned sex.
14. I feel unhappy when someone misgenders me.
15. I feel unhappy because I have the physical characteristics of my assigned sex.
16. I hate my birth assigned sex.
17. I feel uncomfortable behaving like my assigned sex.
18. It would be better not to live, than to live as my assigned sex.

(The original, longer, and more misgendering version of the Utrecht is available here (trigger warning for a really outdated and offensive measurement tool). I would guess GIDS likely used the more offensive and outdated original version. I’ve put the simplified and more modern version above so readers don’t have to get the severe ick that comes from reading the original versions)

They are criticising puberty blockers for failing to show improvements across these 18 questions.

They are criticising puberty blockers for failing to cure transness.

How can we fight this level of bad science at every turn?

Why can’t they even be honest and clear? They could say ‘we expect healthcare to change young people’s answers to the above 18 questions. We consider it a shortcoming of puberty blockers that they do not lead to improved answers to the above 18 questions. We were hoping that puberty blockers would make people not trans. Without evidence of blockers making people not trans, we will not give them to trans youth. Our goal for trans healthcare is to make young people not trans’.

At least be honest about your anti-trans intentions, don’t hide it behind a measurement scale that only gender clinic measurement geeks will understand. Don’t hide beneath a term like gender dysphoria that has multiple meanings.

When stakeholders talk about the goal of NHS services being to ‘reduce gender dysphoria’, if they use the Utrecht scale, they mean, to make people not trans. When they say ‘to reduce gendered distress’ they mean make young people not trans.

When they measure gender dysphoria against the Utrecht scale, they are seeking to cure or reduce transness.

Puberty blockers are ineffective in making people not trans (reducing gender dysphoria according to the Utrecht scale). So, we need ‘talk therapy’, to make people not trans.

 It is conversion therapy all the way through. The conversion therapy is hidden in language of ‘gender dysphoria’ (a term that is used very differently in trans communities’). They know the term gender dysphoria has multiple meanings. It provides a perfect cover for conversive practices.

We need to reduce gender dysphoria they say.

We need to make children not trans they mean.

The level of bad faith, bad science and establishment transphobia is overwhelming. No amount of evidence that affirmative healthcare leads to reduced physical and social dysphoria will ever be enough – because this is not the measure they care about.

They just care about making trans kids into cis kids

This is all they ever care about.

Transphobia and transphobic bad science continues to enable harmful clinical policy and practice.

UK leading the way in transphobic state violence

Last night we learnt that the failing-fast UK government, in one of its very last actions, did something unprecedented, just to make life more un-liveable for transgender children and adolescents in the UK.

They enacted a very rare government power to block access to the only two remaining routes to doctor-prescribed UK-pharmacy-dispensed puberty blockers.

They used an emergency legal power that as far as I can see has only been used once before. That was in 1999 for a barely-known drug that had caused a number of deaths. Even then they went through several steps to gain medical authority scrutiny and approval of government use of emergency powers to enforce a ban, also considering the likely impacts on existing users of the substance (there was no significant use of the 1999 substance that was considered highly toxic).

Yesterday afternoon the UK government used this same rare power to place an immediate (starts 3rd June) emergency ban on puberty blockers a) from overseas prescribers and b) from NHS GPs in primary care.

Let’s start with the second one. The UK government has enacted draconian emergency powers to ban the medical prescribing of NHS GPs in primary care. GPs in primary care already only have ever prescribed puberty blockers as a harm minimisation strategy – where they know a trans adolescent is accessing from a source (eg grey market without any monitoring) and they recognise their duty of care to minimise harms and where the threat to that adolescent’s life is considered severe (adolescents who cannot conceive of living through the wrong puberty). The UK government has made this harm reduction care from NHS GPs illegal. This has now closed literally the last route to UK-prescribed puberty blockers.

The UK establishment has systematically closed every single UK route to puberty blockers. The GMC (the UK regulator of medical doctors) has used its powers against a series of trans positive doctors since the early 2000s (thereby deterring any other doctors from stepping forwards). The CQC has denied approval to any UK private practices seeking to support trans adolescents under the age of 16, meaning the UK registered private providers do not offer support to trans adolescents at the point of puberty. The NHS gender clinics maintained a tight monopoly, with one English and one Scottish clinic for under 18s. The former was closed in March 2024, and the latter has currently blocked routes to puberty blockers. The new English service (also covering Wales) has no route to access to puberty blockers. Every door has shut.

The primary target of the draconian emergency ruling is those who currently receive a prescription for puberty blockers from an overseas doctor. Currently, the vast majority (I would guess 98%) of UK trans adolescents on puberty blockers receive them from an overseas doctor’s prescription, that is dispensed in a UK high-street pharmacy. There must be high hundreds or low thousands of trans adolescents currently receiving puberty blockers via this route. This route will now stop working on the 3rd of June. High hundreds or low thousands of trans adolescents will be without any route to receiving their prescription in a UK pharmacy.

What are those adolescents meant to do? Now they cannot even go to their GP as an emergency and harm-reduction route. Those who cannot or will not consider grey market routes will literally be medically detransitioned, something known to be an actual medical and well-being risk, by the edict of a transphobic government. This will not be safe. This was never about safety.

The power to take this step is based on emergency measures that can only be enacted where there is a critical threat to immediate safety. The government waved this through with the claim “the Cass Review…”.

The Cass Review was a shambles of transphobic medical policy. The Cass review approach to puberty blockers was based on one clever trick.

If the Cass review had asked these two questions, the answers would have been very clear. 1. Are puberty blockers effective at blocking puberty (Yes, very clearly). 2. Are they safe at blocking puberty (Yes, very clearly, used since the 1960s for precocious puberty in children who are 6 or 7, used since the 1980s for trans adolescents, NO EVIDENCE OF HARM).

The trick played by the Cass Review is that they didn’t ask these questions. They instead asked, 1. Are puberty blockers effective at treating gender dysphoria? Shifting to this question allowed them to ignore the very clear evidence that they are extremely effective at blocking puberty. They claimed that effective puberty blockers should improve well-being which has never been the case. Puberty blockers are intended to maintain well-being, in stark comparison to trans adolescents without puberty blockers whose mental health, well-being, wish to live, and ability to succeed at school and socially tends to nose-dive at puberty). Unless you have an unethical study watching the kids who fall off a cliff in mental health without blockers then how do you prove they help prevent a decline in mental health? Shifting the question to whether they ‘treat gender dysphoria’ allowed the Cass Review to state the evidence of effectiveness was ‘inconclusive’.

Secondly, instead of asking whether the medicine is ‘safe’, they asked a narrower question, is it ‘safe in treating gender dysphoria’? This allowed them to disregard decades of studies that puberty blockers are safe when used in cis children. The drug is very clearly safe. It is still today (and next week) prescribed by the NHS for younger children who are not trans. There are no safety concerns. The medication is clearly safe.

The only way that the Cass Review was able to raise any safety concerns at all, was through transphobic speculation. They speculate, with zero evidence, that perhaps puberty blockers may ‘change the outcome’, keeping a trans child as a trans adolescent, when all they need is a good dose of their endogenous hormone and then they would turn out normal (cis). (See my recent podcast transcript that dives into this). The severe safety risk that the Cass Review speculates about, is the risk of still being trans. There are some other speculations, that are only proposed for trans adolescents (not for cis youth receiving the same medication for any other purpose, including endometriosis or early puberty). None of the speculations are evidenced. The Cass Review also references things like bone density, which is a minor risk that endocrinologists are well aware of and can be easily managed by a) monitoring bone density b) taking vitamin supplements c) not being on blockers without hormones for more than a couple of years. There is no evidence of actual risk or actual harm at all of trans adolescents using puberty blockers.

The actual risk is, of course, the opposite. There is a very real risk to trans adolescents who need puberty blockers and are denied them. In the last week I’ve spoken to two parents whose children no longer wanted to be alive because of starting to be pushed through a puberty that is distressing and humiliating for them. For adolescents who are deeply distressed by puberty, instead of being offered a safe and effective medication that can stop those changes, they are being offered a big pile of nothing. They are being offered the suggestion that perhaps they are not really trans, and perhaps the changes that they find traumatic are just want they really need to grow up cis. That is where we are with trans healthcare in the UK today. Trans children and young teens are being told, ideally you should convert yourself into a cis person, or we literally do not care for you, your life, your safety, your well-being.

High hundreds or low thousands of trans adolescents who are on puberty blockers, happy and healthy, will be forceably detransitioned by government edict, without medical supervision or support, starting on the 3rd of June. Some of these will turn in desperation to grey market sources, finding every route to UK pharmacy dispensing closed. There are risks to youth who are forced onto grey market sources, both in terms of ensuring the quality of medication that does not come from UK pharmacy, and perhaps even more so in terms of the risks associated with healthcare avoidance. Trans adolescents who are accessing grey market medication, having had every other route banned, will be reluctant to go to their GP for other health issues. There is a real risk of a whole generation of trans adolescents losing out of mainstream healthcare, and becoming at higher risk of the health impacts that occur when a portion of society is afraid of talking to their GP or health service. Communities who are afraid of talking to their healthcare providers (see undocumented immigrants) are likely to go to healthcare providers late when they have a routine health concern, are likely to wait until minor healthcare concerns become major, are likely to have significantly worse general healthcare outcomes. This is where we are heading today for trans adolescents in the UK. It is an absolute oppression. It is not about safety. It was never about safety.

The emergency legislation lasts for only 3 months, as the UK government is enacting an emergency power intended for a new and unexpected threat to life, not a power intended for a medication safely used since the 1960s. This temporality does not reassure me. Let’s look at the Labour Government’s reaction – are they going to condemn this transphobic intervention as dangerous and abusive government overreach into healthcare? I bet they will not. And if they do not, then I have no confidence that they will not extend this if they are in power come September.

In the name of ‘safety’ the UK government is making the UK more unsafe for trans adolescents. Transphobia is the biggest safety threat to trans adolescents, as to trans people of all ages. Trans children and adolescents can have a happy and safe and secure childhood and adolescence. But the UK government and the NHS is trying its utmost to take that happiness and safety and security away. We need to do better for trans young people. #TransRights #TransKidsShouldThrive #TransHappinessMatters

Ten Dangerous Cass Review Recommendations

The Cass Review final report has now been published. It has been received with jubilation by transphobic hate groups, by conversion therapy proponents, by those advocating against trans rights, by those who do not believe in the existence of trans children. The report has been praised and endorsed by all major UK media outlets, by MPs from the Conservatives and Labour, with both main parties committing to the fulfilment of all Cass recommendations.

The report has been met with horror and fear by trans communities, by trans healthcare professionals around the world, by families supporting trans children. Trans healthcare scholar Ruth Pearce has collated such responses here.

The Cass Review is biased and prejudice-driven in its design, delivery, analysis and approach to evidence, as documented in my peer reviewed analysis, published in the leading journal for trans healthcare.

In this short blog I will not revisit the very many methodological, conceptual, interpretive, evidencial and policy failings of the Cass Review. Instead I will here summarise and very briefly comment on ten significant recommendations of the Cass Review, each of which will cause significant harms to trans children. Here I am summarising ten of the recommendations that have me concerned, drawing from across the full 400 page report. These are not the recommendations that Cass has chosen to draw attention to in the 5 page summary document (these are analysed by Gemma Stone here) but are recommendations embedded across the longer Cass Review document. Each of the recommendations summarised below is built on a foundation of prejudice, ignorance, cisnormativity and pathologisation of trans lives, running in direct opposition to the evidence base, and running in direct contravention of an NHS duty of care to children’s rights, children’s welfare, healthcare equality and healthcare ethics.

These Cass Review recommendations have already been endorsed by powerful politicians from both the Tories and Labour. They have been endorsed by powerful healthcare stakeholders from BPS to BMJ, and there is significant high level commitment and motivation to quickly rolling these recommendations out into practice in the NHS. This roll out is a very significant safeguarding risk for trans children in England and Wales (where I refer to the NHS from here onward, it refers to the NHS in England and Wales).

  1. A current complete ban on NHS access to puberty blockers.

The Cass Review recommends a complete ban on access to puberty blockers outside of a research trial, with the research trial not yet developed. There is no current route to trans children accessing puberty blockers through the NHS. All previous access routes have been closed and no new children are accessing blockers. This is not labelled as a complete ban (although it is a complete ban currently in practice) as there is reference to a potential future research trial. NHS documents have been very clear that the current ban will continue even if the proposed research trial never commences. The trial has not yet been developed, and it is unlikely that such a trial would ever receive ethical approval to commence. Even if a trial does at some future point go ahead, it is likely to be highly restrictive and unethical.

2. Legitimisation of conversion therapy

The Cass Review recommends therapeutic practices that run counter to an affirmative approach that welcomes trans lives as equal to cis lives. The Cass Review endorses ‘exploratory therapy’, a re-branded title for conversive practices. The Cass Review is careful to avoid actively calling for conversion therapy, but Cass has appeared in the media since the report’s launch speaking against a ban on conversion therapy, highlighting that such a ban could impede the type of ‘therapeutic practice’ that Cass recommends.

3. Intrusive and abusive ‘assessments’

The old GIDS service was criticised for assessments (as part of gaining approval for transfer to endocrinology) that were abusive and intrusive. Cass recommends the new service takes this intrusive approach to questioning a step further. Here this is not even a discrete step in eligibility for endocrinology (as under 16s will never be eligible for medical intervention) but an ‘assessment’ for its own sake, enforcing a prolonged intrusion into trans children’s lives. Cass recommends that trans children are questioned on a bewildering range of intrusive topics, on sexuality, on masturbation, on porn viewing, on experiences of abuse, on family violence, on mental health, on anything and everything that could have influenced them to be trans. This type of expanded questioning deeply problematises transness, and is a deeply pathologizing and abusive approach for children who just happen to be trans. It is particularly harmful for the trans children who are without support, who are left feeling there is something deeply wrong or shameful about who they are to justify such ongoing intrusions. In the old GIDS intrusive ‘assessment’ was tied to referral to endocrine services, with at least a theoretical end in sight. In the new system I see no safeguards to protect trans children from intrusive assessments that never end.

4. An immediate removal of 17 year old access to adult healthcare clinics

The Cass Review recommended an immediate cessation of 17 year olds being able to access adult gender clinics (an approach that had been adopted following the huge delays in children’s services). NHS England immediately adopted and actioned this recommendation, pulling away hope from trans adolescents. Trans youth who have already been waiting for 5+ years for access to healthcare, who some of whom were counting the weeks to the 17th birthdays, have had this hope immediately pulled. Some 16 year olds are taking this news very hard. The NHS does not have any idea or concern for the well-being of trans adolescents who are left without healthcare.

5. Clinical control over social transition

The report recommends caution on social transition, proposing that showing respect and support for a trans child be considered an active intervention that necessitates engagement with clinical services, and by inference, clinical oversight. The process and timelines for gaining clinical permission to socially transition are unclear, but I can foresee children waiting years without clinical permission to socially transition, especially for younger trans children. Delays to social transition are harmful, shaming, and abusive, with a direct impact on trans children’s happiness and mental health. Delays to social transition are a form of conversion therapy. This approach will have particularly damaging implications for trans children in care, where care providers or foster carers may not feel able to support a child without clinical permission. It is also likely to increase delays and barriers to social transition in families who are lacking in trans-positivity, or where parents are divided in their supportiveness. My recent peer reviewed article on social transition synthesised all existing evidence on social transition, with a wide range of evidence of the benefits of social transition, and zero evidence on harm.

6. Potential restrictions for young adults

The Cass Review has already expanded into having a view on adult trans healthcare, proposing a Cass-style review of the evidence base supporting trans adult services. Given the major flaws and prejudices of the children’s Cass Review, any parallel endeavour in adult services is a very significant concern. The Cass Review talks in vague terms about changing the service for 18-25 year olds. This raises concern that this will lead to barriers to healthcare for young adults. It does not seem a coincidence that this vague recommendation aligns with the policy priorities of anti-trans actors who have long sought to restrict healthcare access for 18-25 year olds – indeed the Cass Review relies upon exactly the same flawed and misinterpreted studies on brain maturation that are used by anti-trans campaigners to advocate that trans adults are too young for mature decision making.

7. A ban on peer concordant puberty (with severe HRT restrictions even for 16 and 17 year olds)

Best practices worldwide for trans healthcare includes the option of trans adolescents taking HRT at the same time as their peers. There is growing evidence that peer concordant puberty is important for emotional well-being, physical health and educational attainment. For many trans youth, waiting until 16 to access HRT is too late, with implications for their mental and physical health.

The Cass Review recommends that even HRT at 16 and 17 be seen as an exception, with a majority denied any access to medical intervention until adulthood. The Cass recommendations to restrict HRT to 16 year olds also appear to make it harder for those who have accessed puberty blockers and HRT privately to transfer back into NHS services at 16, completely isolating trans under 18s who have gone private from returning to NHS healthcare. These approaches lead to significant inequalities between those who can access private healthcare and those who cannot, between those with or without the financial means to afford private healthcare until age 18.

8. Recommends CQC restrictions on private healthcare

The Cass Review recommends the Care Quality Commission intervene in private healthcare provision to ensure Cass recommendations are equally enforced in private healthcare. This ensures the Cass approaches, with their ban on puberty blocker access, their intrusive questioning, their ‘exploratory’ therapy, is the monopoly approach in the UK, preventing the development of any affirmative provision in private or non-GIC healthcare services. This is immediately a threat to any existing services who want to provide affirmative healthcare for trans 16 and 17 year olds outside of the Cass model. It also provides a more significant barrier to any future CQC registered private providers supporting trans under 16s. This guidance reinforces the monopoly of the Cass position.

9. Recommends Pharmaceutical Council intervention in overseas prescriptions

The Cass Review recommends the General Pharmaceutical Council takes action to prevent pharmacies from fulfilling gender affirmative prescriptions from overseas clinics. In a country where there are zero NHS or CQC registered healthcare providers prescribing for trans under 16s, action to prevent or deter pharmacies from fulfilling private prescriptions would close down the only current route to healthcare for trans under 16s. This would force desperate families into emigration or black market provision. Cass has no consideration of the NHS’s duty to adopt a harm reduction approach.

10. Problematisation of trans identities

The Cass Review has worsened pathologisation and problematisation of trans identities, legitimising those who seek discrimination under the banner of it being justified to ‘protect children’. The Cass endorsed problematisation of transness has implications for how trans children and trans communities are treated across our society.

The Cass Review reinforces a number of myths about likely parental, social, peer, abuse or porn related influences on a trans child’s identity. There is no acknowledgement that some children are trans and this is fine (or even to be celebrated). There is no recognition that being trans is a healthy part of human diversity. This message and the concerns around negative factors that can cause a trans identity in childhood can be devastating in sphere like family courts, social services, schools. It is likely to discourage parental support and provide legitimacy to abusive anti-trans families. These messages of a trans child being created through outside influence can be particularly harmful in custody battles between affirming and rejecting parents. There is no consideration of the need to protect and safeguard the well-being of trans children.

Fear, hope and resistance

Last night I couldn’t sleep.

Today I can hardly breathe.

The weight on my chest and heart and spirit feels too much to bear.

In the UK right now, as a trans person, as a parent of a trans little person:

  • I do not feel safe
  • I do not feel hope
  • We do not feel safe
  • We do not feel hope

How do we protect those we care about from a society where there is so much hate. So much prejudice. So much injustice. So much indifference.

How do we endure such overwhelming oppression?

I’m trying to help my child stay afloat in the face of injustice and persecution. I’m trying to keep us afloat. But it is rough. It has been rough for years and keeps getting rougher. I am tired of the struggle. We are all so tired.

  • I can’t withstand this on my own.
  • My child can’t withstand this on her own
  • We can’t withstand this on our own.

We need community. We need solidarity. We need resistance.

I feel particularly isolated and alienated (and gaslit) when I see supposed allies participating in our oppression. Seeing a prominent LGBT org ‘welcome’ the Cass Review felt like a stab in the heart. Over the past few years I continue to feel let down by UK civil society. The child rights or LGBT or trans rights organisations who look the other way, who do not stand with trans kids, who minimise current harms

As we face and endure state violence, it hurts to see parts of civil society complicit in such violence.

We need ‘allies’ to call out state violence and systemic oppression. Instead too many are afraid to challenge the Cass Review – too afraid to challenge the opinion of a medical doctor, even when the approach and findings are so clearly wrapped in prejudice. Instead staying quiet or siding with our oppressors.

It is not good enough.

We are all sinking.

So many trans folks I know are struggling right now. I’m struggling. So many trans kids I know are struggling.

We need to acknowledge state violence. That is a very low expectation of our supposed allies.

We need to acknowledge systemic oppression and persecution.

We need to be talking about strategies of resistance.

Trans communities, and especially trans children, need to resist state violence in the UK right now. Trans kids need to resist and endure the violence endorsed and recommended in the Cass Review, the violence in government policy, in media discourse, in school policy, in hostile and abusive homes.

Now is not the time for complicity in such oppression.

Now is the time for reaching out to trans people who are scared and without hope. I have a lot of relative privilege, and I am scared and low on hope today.

Now is the time for those of us with any privilege or power to stand up and be counted. Now is the time to pull together, acknowledging state violence and oppression, and focusing on strategies of resistance.

It is not easy to resist state violence. Especially for a child.

It is not easy to support a child to resist state violence, especially when isolated and threatened.

We all need hope. We all need community. We need genuine solidarity.

None of that can come from denial or minimisation of current harms.

We need to acknowledge that the UK is a seriously hostile location for trans people and especially trans children. We need to talk about resistance and survival.

We need to support each other. We especially need to support the trans children we know and love, to withstand the many current injustices, and those we see on the horizon looming down on us.

Solidarity. Justice. Resistance.

Sending love to all who are struggling. Sending love to all who will help. We need each other.

Cass Review Final Report – Media Briefing

The Cass Review final report is released tomorrow. I’ve seen the summary and it is as expected.

After a 4 year process the Cass Review final report is a deeply depressing outcome. I have repeatedly, over many years, called for paediatricians to take a role in trans children’s healthcare. In other countries paediatrician-led care has helped shift trans children’s healthcare from harmful and pathologising conversive practices endorsed by those who treat transness as a mental health disorder, into modern, child-centred, trans-positive healthcare. In this, Dr Cass has failed.

The Cass final report fails to take any meaningful steps to improve the lives of trans children. It fails to depathologise trans lives. It fails to centre trans children’s rights. It provides a veneer of credibility to policies, practices and systems that are backwards, pathologising, abusive, and deeply damaging to trans children and young people.

The Cass final report repeats the failings of earlier Cass publications. I have published a peer reviewed analysis and critique of all earlier Cass related reports in the leading journal on trans health (the International Journal of Transgender Health). This analysis highlighted four major concerns with the Cass approach and outputs.

The Cass Review: Cis-supremacy in the UK’s approach to healthcare for trans children

These concerns relate to (1) prejudice; (2) cisnormative bias; (3) pathologisation; and (4) inconsistent standards of evidence.

Each of these concerns impacts the Cass Review’s approach to trans children’s healthcare, with negative repercussions for trans children’s healthcare rights and well-being.

Trans children face unbearable challenges at present in the UK. The scale of hurt, pain and trauma is hard to describe.

There is currently no accessible NHS healthcare for trans adolescents, in part due to the Cass Review. Newly proposed centres will not offer timely affirmative medical intervention, care that is recognised as essential and life-enhancing for many trans adolescents.

There is a real risk that professionals in new NHS centres will be emboldened to adopt pathologising conversion practices that cause immense harm. The Cass Review’s ‘caution’ on social transition will lead to more trans children enduring the harm, shame and trauma of delayed or denied transition, with significant consequences for trans children’s self-esteem and mental health. There is a growing body of global evidence on the benefits of social transition and no evidence of harm. Current guidance will deny many trans children the chance for a shame-free and joy-filled childhood.

Trans children face severe barriers to equality in education, with many experiencing trauma in UK schools.

Too many trans children face rejection and abuse at home, including from families who are mis-led into anti-trans practices by lobbying organisations who fundamentally reject the very existence of trans children.

Trans children face harm and injustice at every turn. The Cass Review’s final report does nothing to help trans children live happy, healthy, safe and confident childhoods.

I hope that those who actually care for trans children will take action today – calling out the dire situation for trans children in the UK and highlighting the failures of the Cass Review. I hope more people will stand up alongside trans children, resisting the most outrageous harms, and defending trans children’s rights.

Trans children have a right to safe, supported and happy childhoods.