PSSD Foundation
Re: PSSD Hilfe Deutschland e.V.
Great work!
- Medical Student & Friendly poltergeist - Lexapro Sept '14. [Hx] [PSSD Lab] [r/PSSD] [Treatment Plan] - Add "Ghost" in replies so I see it 
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fema4psyciatrists
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Re: PSSD Hilfe Deutschland e.V.
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.
RIP Ali 23 years old
RIP Kevin Goodreau 28 years old
RIP Petar 23 years old
RIP Mary Koback 22 years old
RIP David Stofkooper 23 years old
RIP SadBoy
RIP Kata Balint 28 years old
RIP Kevin Goodreau 28 years old
RIP Petar 23 years old
RIP Mary Koback 22 years old
RIP David Stofkooper 23 years old
RIP SadBoy
RIP Kata Balint 28 years old
Association for PSSD
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.
So, what are your ideas in terms of making one for us PSSD suffererer's. Just to hear your ideas on this.
Re: Association for PSSD
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.
Fluoxetine 2008-13, PSSD thereafter
Condition worsened after 4 weeks on Setraline in 2014
Condition worsened after 4 weeks on Setraline in 2014
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Ciprofloxacin
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Re: Association for PSSD
The most logical post I have ever seen.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.
Re: Association for PSSD
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.
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.
Will there ever be a PSSD Foundation?
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'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.
Sertraline jan-jul 2018
Re: Will there ever be a PSSD Foundation?
I don't have idea why there is none too. High time.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.
Finding a cure is only a matter of time! Never quit!
Re: PSSD Foundation
Several topics merged. This is where all future PSSD foundation info will be posted.
- Medical Student & Friendly poltergeist - Lexapro Sept '14. [Hx] [PSSD Lab] [r/PSSD] [Treatment Plan] - Add "Ghost" in replies so I see it
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