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Andrew Orr's avatar

It has only taken all the years from 2017 to have the documented email evidence revealing the FDA in the U.S. was then ( and presumably remains) ideologically captured from within , when the senior endocrinologist within the statutory bodyโ€™s policy determinations can advise support for puberty blockers in minors, after being informed by an empathetic โ€œ listening โ€œ by others. To not be wanting to pursue official blessing from the current โ€œ off labelโ€ status of the use of GnR agonists might be in the knowledge that there would be predictable difficulties in obtaining evidence for benefit, over potential harm. Our own TGA is likely, for the same reasons, to not be approached by the activists to obtain approval for use by the same gender affirming clinicians. Best not to test the regulatory bodies in both countries! . Bernard , I remain curious about any role which might have been played in the NHS Englandโ€™s challenge and closure of Tavistock. I donโ€™t recall any such discussion during the recent NAPP hosted webinar with Hillary Cass. We know our AHPRA is but an agency of government and only able to respond to complaints ( rather than act as an independent investigatory body) , perhaps a more proactive response might be expected from our TGA? Just a , likely naive, thought ?

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John Traffas's avatar

Just yesterday (8/2/24; https://www.city-journal.org/article/the-deposition-of-meredithe-mcnamara) Leon Sapir wrote of "Yale report" co-author Dr. Meredith McNamara: "The transcript of that deposition [in the case brought against an Alabama age-restriction law] reveals that McNamaraโ€™s many public and under-oath statements about her clinical experience are fundamentally misleading, if not outright falseโ€”and even perjurious."

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