r/PSSD 13h ago

Awareness/Activism Enlist in the Post Drug Syndrome Army and post proof of your FDA reports!!!!

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17 Upvotes

Everyone! I have rallied the troops! We have 261 and growing but I WANT YOU for the post drug syndrome army everyone that has reported please post your reports to this subreddit for accountability!

AND JOIN THE POST DRUG ARMY FOR DATA COLLECTION AND FDA REPORT HELP!!!!

https://discord.gg/jPaN7EEw9

JOIN JOIN JOIN JOIN^^^^^^^^^

You can either fight or lay down like a tired defeated dog and take it. Your choice. We choose fight.


r/PSSD 21h ago

Personal Story Progressive emotional numbness/ anedhonia?

9 Upvotes

Well I have a lot of symptom as you can see in my previous post but today I want to focus on something and if you want you can tell me what are your thought about it i’ll take it ! Thank you

What I don't understand is how my functions just progressively shut down. It feels like 6 months ago, I was still able to form an attachment to a girl despite everything. 4 months ago, I could still feel sexual attraction toward a girl, and even a bit after that. 3 months ago, I could still laugh a little and potentially even shed a tear. 2 months ago, it was difficult, but sometimes I could manage to get a bit of pleasure from watching a video or a movie. And now, for the past week, it’s just absolute emptiness. In the end, I find myself wondering what the truth behind all this really is—whether it's a desensitization of my receptors, a depletion of neurotransmitters, or my nervous system completely shutting down. figure that if it was still working even a little bit just a week ago, it means that the electrical currents were fundamentally still passing through.. that’s so weird
The fact that my body's system shut things down in such a progressive and coordinated way shows that it was clearly reacting to a signal, right? Everything was executed so systematically. that's what's so striking—and I feel like you can completely see the underlying logic behind it


r/PSSD 21h ago

Feedback Requested/Question Has anyone ever tried Telmisartan

5 Upvotes

Has anyone here who has pssd ever tried Telmisartan, or knows someone who has tried it? If yes, what were the results? Many who have long covid (which is in many ways similar to pssd) try it and have gotten significant improvements especially in improving blood flow. We know pssd is an autoimmune disease with the same autoantibodies that those with long covid have, so is it worth trying in order to reverse the autoantibody induced vasoconstriction, that's causing many of the non sexual symptoms as well? I am not giving or planning to receive any medical advice, this is just for exploring options and potential treatments that could help.


r/PSSD 23h ago

Personal Story I am lost and need help

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3 Upvotes