I don’t think it is nearly as bad as the video makes out, but it is a statement effectively aimed at reining in NHSE.
It talks about “artificial binary opposition between exploratory and affirmative approaches”, but the affirmative approach at a minimum hampers exploratory therapy and at worst prevents the child from being able to engage in it. NHSE will need to be absolutely clear about the approach therapists will take because any hint of affirmation in the final service specs will lead to the status quo with the new regional centres insisting they undertake exploratory therapy but in an affirming environment.
it talks about children and young people who “require” a medical pathway or medical intervention. Particularly in the absence of an evidence base for the medicalisation of children and young people, which ones “require” medical interventions and how will this be determined? Particularly when considering that this is an area of healthcare with no certainty and clinicians openly admitting this (eg episode 2 of the Tortoise podcast where Polly Carmichael witters on about thriving on uncertainty).
There appears to be a move away from social transition as a medical intervention (as NHSE have made clear it is). They seem to have gotten themselves into a muddle over clothes and hair after the unfortunate misinterpretation in some of the press (and picked up by the lobby groups) about restricting these. Social transition is more about the people around the child than the child themselves. The child already sees themselves as the opposite sex - it’s not about the hair or the clothes, it’s about other people embedding the child’s belief that they are the opposite sex by use of preferred name/pronouns etc. NHSE have made it clear this should only happen under certain criteria including a gender dysphoria diagnosis and under clinical supervision
Obviously you can’t change the child’s or their peer group’s use of name/pronouns/reinforcements, but as a medical intervention, a clinician can make a recommendation about how the adults in the child’s life should react to this. The Cass Review is saying: “The role of the professional is to facilitate parents/carers, children and young people to engage in an in-depth process of discussion and thinking around this decision…” which is quite different to the NHSE position.
If the service ends up the way the Cass Review has responded to the NHSE consultation, it will be fundamentally no different to the current service (other than the PB trial). They will be asking parents to effectively take a leap of faith despite their being no evidence base for what is being recommended, and their recommendation is still very much child led. I can’t see parents on the more cautious side buying it. Neither side trusts the NHS in this issue but ultimately, there is no middle ground and a decision will need to be made as to which direction to take.