I think anyone commenting on Cass research should have their expertise to do so established very clearly before any weight at all is placed on their opinion.
The Cass project, or approved researchers seeking to access health records and GRA status information under strict legal oversight for approved purposes is not ‘fascist’. What an insult to the millions of victims of fascism.
The Cass review is not going to be making any kind of opinionated judgement on the concept of child transition. My understanding is that they are simply looking to discover what has happened over time (judging by the health records) to children who have medically transitioned and this group will include some of those who will have as adults gone on to get a GRC. (Not all children who transition will want to get a GRC.) When they have this info they will make it public.
All of which is urgently needed information to inform and improve the quality of care for children, because the physical and emotional consequences of taking medical or surgical transition can be so severe and permanent. And because currently they can be decided by children who can’t possibly be expected to understand the full meaning of what they are giving up. And what they are taking on in terms of health problems. I think it’s a misapplication of Gillick competence.
That’s also another argument for the GRA to be updated to allow research using data from people who do get GRCs. It sounds like it’s not possible research for researchers in general to apply to do that (because only allowed for the Cass review ones for next 5 years. Why is that?). Isn’t that in itself an argument for GRA reform?
Adults who live as transmen or transwomen may or may not medically and/or surgically transition as part of that and they may or may not get a GRC at some point in their lives.
Enabling GRC data to be used in research would allow comparisons of outcomes to be made between those adults who get GRCs and those who don’t and to look at what medical interventions they may (or may not) take on in the course of their lives relative to the GRC application.
Having publicly-available research data on all of that could better inform trans adults impartially about their options, could inform better ways of the state supporting trans adults who want to change their legal status. Research evidence could also inform making sure the health care provided to trans adults is as safe and effective as possible at supporting their needs and could be used to look at where that could be done better.
So banning research on the data of people who get GRCs in fact means that researchers lose an important comparison group for all of the groups under the very wide ranging ‘trans umbrella’. Which means all trans people lose out on important information.
Taking an anti-research position calling for a whole community not to support it, in fact asking people to just stop short of putting ‘tanks on the lawn’ to actively try to prevent it happening, seems incredibly selfish and individualistic, not to mention intimidating, whatever way you look it.
It seems a very odd position for anyone to advocate that a caring, inclusive, health-conscious community ever would want to adopt.