u/Prudent-Process5377

Im wondering, this is important

Wondering this is important

Wondering

It’s so frustrating. It can’t be a councidence atp. Who is the health team? We need to at least try out a new team, and see if anything improves.

Is it possible to implement a sim 10 years feature? Madden has this feature and it makes it very nice to test settings or otherwise with.

Such as if parnate recovered you, what signs were there earlier on the first week or so of taking it? Such as energy moving inside your body or this little clues that you were going to recover.

He’s truly generational imo

I’ve been trying to find other people with a condition similar to mine, but almost every severe case I come across is related to PSSD, drug use, or medication withdrawal.
My case appears to have developed naturally, and my symptoms are extremely severe:
Near-complete inability to experience pleasure (music, food, hobbies, games, accomplishment, etc.)
Emotional numbness with almost no excitement, comfort, anticipation, or reward
Almost complete loss of libido and sexual pleasure
Feeling like my brain’s reward system is “offline”
Very little anxiety emotionally, despite obvious physical stress responses
Severe lack of motivation that feels neurological rather than psychological
I’ve been diagnosed with severe melancholic depression and am currently undergoing ECT after many medications failed.
I’m **not** looking for a diagnosis. I’m mainly wondering:
Did anyone else develop something this severe **without** SSRIs, recreational drugs, or another obvious trigger?
If so, what do you think caused it?
Did you recover, partially or fully? If you did, what helped the most?
Did your symptoms resemble PSSD despite never taking an SSRI before the onset?
I’ve felt pretty alone because almost every story I find has a medication trigger, and I’m trying to figure out whether there are others whose brains seemed to shut down naturally.
Any experiences would be greatly appreciated.

I’ve been trying to find other people with a condition similar to mine, but almost every severe case I come across is related to PSSD, drug use, or medication withdrawal.
My case appears to have developed naturally, and my symptoms are extremely severe:
Near-complete inability to experience pleasure (music, food, hobbies, games, accomplishment, etc.)
Emotional numbness with almost no excitement, comfort, anticipation, or reward
Almost complete loss of libido and sexual pleasure
Feeling like my brain’s reward system is “offline”
Very little anxiety emotionally, despite obvious physical stress responses
Severe lack of motivation that feels neurological rather than psychological
I’ve been diagnosed with severe melancholic depression and am currently undergoing ECT after many medications failed.
I’m not looking for a diagnosis. I’m mainly wondering:
Did anyone else develop something this severe without SSRIs, recreational drugs, or another obvious trigger?
If so, what do you think caused it?
Did you recover, partially or fully? If you did, what helped the most?
Did your symptoms resemble PSSD despite never taking an SSRI before the onset?
I’ve felt pretty alone because almost every story I find has a medication trigger, and I’m trying to figure out whether there are others whose brains seemed to shut down naturally.
Any experiences would be greatly appreciated.

I’m experiencing loss of cognitive function after my first bilateral treatment and I’m wondering if receiving cognitive function loss so soon means it’s likely or not likely that I will get permanent cognitive damage if I continue.

ects. The main issue has been a noticeable decline in memory recall, including difficulty remembering recent events from the past few days, recalling familiar information, remembering my ECT schedule, and briefly forgetting routine tasks. My overall cognition feels reduced, with difficulty thinking clearly, engaging with intense content, and processing information without discomfort. Attempting to think deeply or concentrate causes a constant mental/head pain sensation. Earlier after treatment, I also experienced significant sensitivity and pain in my temples/scalp, which has since improved, but the deeper mental pain and cognitive slowing remain. I have felt mentally foggy, with reduced ability to retrieve memories and a sense that my brain is not functioning normally compared with my baseline. These symptoms began after the bilateral ECT session and were noticeably different from my experience with unilateral ECT, where I did not experience comparable memory problems or head sensitivity.

Do these symptoms resemble closer to cases that have permanent cognitive damage, or just temporary cognition problems post ect? How quick should these resolve?