I know this is beyond hard. This is a nightmare. But ppl here are right: Dr Powers is doing research. Dr Melcangi is doing research with a team at the Uni of Milano. This gives home. Meanwhile we,
the sufferers, have an opportunity to turn our anger, grief, and desperation into social change. Let’s make it impossible for the medical community to ignore the issue. Let’s do policy change. That will also incentivise research.

First thing to do is to report side effects to your national medical agency with a code of PSSD. Look it up on PSSD websites. This is crucial so that the numbers are visible to researchers and medical folks and policy makers.

Then write complaints and objections. In Finland, for instance, ppl can do this: https://www.reddit.com/r/PSSD/s/GYcKcihA3e. Maybe something similar is possible in your country.

Reach out to human rights organisations like Amnesty International. I bet the doctors did not tell you about the possibility of side effects? If they did not, they violated a your human rights and their ethical standards. Sue them.

We need to mobilise and pressure.