PSSD Forum

Great work!

Great work! I have started running and running my first marathon campaign. I hope I can continue and do the next one for this PSSD foundation and our studies.

Guys i was noticing that some studies have been made on PFS. They have a good organization with a fundation,unfortunately we don't have any.
So, what are your ideas in terms of making one for us PSSD suffererer's. Just to hear your ideas on this.

How about making an association for Post SSRI syndrome which promotes research for all the symptoms we experience, not just sexual? I think thats why the PFS foundation is so great, it raises awareness of how complicated and varied what we term 'PSSD' can be.

omar90 wrote:How about making an association for Post SSRI syndrome which promotes research for all the symptoms we experience, not just sexual? I think thats why the PFS foundation is so great, it raises awareness of how complicated and varied what we term 'PSSD' can be.

The most logical post I have ever seen.

That's what i was talking about.
Maybe, even an official website for PSSD could be useful.
The studies seem to indicate that the problem is underestimated, there could be many others, and if things are like these it's important to spread the awarness.
I'm afraid that no one would have interest in the problem and no study will be run unless we make something.

Hello

I'm wondering why there isn't a PSSD Foundation yet... it would be so nice if there was one, so we can get more recognition, money and research so things can move a lot faster.

Please share your ideas, opinions and suggestions about making one.

Knifli wrote:Hello

I'm wondering why there isn't a PSSD Foundation yet... it would be so nice if there was one, so we can get more recognition, money and research so things can move a lot faster.

Please share your ideas, opinions and suggestions about making one.

I don't have idea why there is none too. High time.

Several topics merged. This is where all future PSSD foundation info will be posted.