PSSD In Person Meet Up Event
PSSD In Person Meet Up Event
Anybody interested in having a PSSD In Person Meet Up Event? I'm actually serious about this. Would you be brave enough to reveal who you are and show up in person to a nice warm vacation spot like Disney World for a PSSD meeting? We can watch presentations on PSSD at Cinderella Castle. Then we can go ride Space Mountain and the tea-cups. Then at night time we can go to Downtown Disney or some strip clubs with backpacks full of supplements and go up to every girl possible and ask them if they want to bang. Each night would be a different experiment with a multitude of supplements and different girls. Maybe some of us would be fixed. I know it sounds ridiculous but life is really short and there has to be some way that we can gather and come up with ideas faster. There's HIV/AIDS in-person support groups and I imagine that must be quite embarrassing as well (and for some reason Magic Johnson is still alive and healthier than all of us...mindblowing huh?), so really...why not a PSSD in person support group at this point?
I was forced onto Prozac back in the mid 1990s as a minor giving me PSSD then either forced or coerced to take 40+ different psychiatric medications resulting in severe iatrogenesis.
Currently on 1125 mg Depakote Sprinkles, 3 mg Klonopin.
Currently on 1125 mg Depakote Sprinkles, 3 mg Klonopin.
Re: PSSD In Person Meet Up Event
PSSD is a very personal problem many people can barely even talk to their closest family members/partners about. Also i don't think that many people would be willing to spend hundreds of dollars to fly somewhere and talk about this in person when this forum works just fine. Between having expensive as hell blood tests and trying different substances i don't think too many people here have that much extra money laying around for this. Just my thoughts
Re: PSSD In Person Meet Up Event
Fuck yeah I would!
Re: PSSD In Person Meet Up Event
Ive often thought about how much I’d like to meeting up in person over a weekend and have a handful of panels/ chats on different pssd topics and hopefully a few experts on hands to join.
I’m not sure how serious you’d comments about taking a load of supplements and ‘testing’ these on random girls were, but if serious then I have to say that sounds a bit ridiculous. But in terms of a more serious meet up I’d be keen. We’re all around the world though, so probably a logistical nightmare and realistically money would be better spent on meds. If enough people were interested I’d be up for a conference call or something, and again - great if we could get an expert on the calll
I’m not sure how serious you’d comments about taking a load of supplements and ‘testing’ these on random girls were, but if serious then I have to say that sounds a bit ridiculous. But in terms of a more serious meet up I’d be keen. We’re all around the world though, so probably a logistical nightmare and realistically money would be better spent on meds. If enough people were interested I’d be up for a conference call or something, and again - great if we could get an expert on the calll
Re: PSSD In Person Meet Up Event
Seriously folks, I think it's a good idea.
We should all meet and demonstrate in front of pharmaceutical buildings, write letters to medical institutes, doctors, prosecutors etc.
Then we would get attention very quickly as the people at that time with the PFS syndrome.
But instead, the people would rather howl in the forum every day how bad you are. I think it's cowardly ...
We should all meet and demonstrate in front of pharmaceutical buildings, write letters to medical institutes, doctors, prosecutors etc.
Then we would get attention very quickly as the people at that time with the PFS syndrome.
But instead, the people would rather howl in the forum every day how bad you are. I think it's cowardly ...
June 2015 - April 2016 Fluoxetine
April 2016 - March 2017 Fluvoxamine
December 2017 9 days Trazodone
After Trazodone PSSD: loss of libido & spontaneous/night/morning erections, prostate/pelvic pain, genital numbness, lower sperm count, Anhedonia
April 2016 - March 2017 Fluvoxamine
December 2017 9 days Trazodone
After Trazodone PSSD: loss of libido & spontaneous/night/morning erections, prostate/pelvic pain, genital numbness, lower sperm count, Anhedonia
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Re: PSSD In Person Meet Up Event
You do realize there is female members here don't you? To say those comments were distasteful would do them an injustice. A man that would spew such stuff then call me cowardly.... yeah my ego is really hurt.
Write prosecutors? No law has been broken. Write doctors? That would get us as far as when people go to their own doctor and get that "I don't know." Write medical institutions? Ok Ill put aside the wrong use of the word as I think I understand what you meant. That could be a viable course of action but before could present anything we need to be able to quantify it first. Just saying "so and so feels this way" doesn't mean jack to the medical profession.
As to Kk88; would be nice in theory but sadly there is no experts. As far as doctors are trained we should not exist. People like to think that doctors don't WANT to understand us; that's just not the case. People need to stop and think that being a doctor is a job. Just like our jobs; we was educated or trained to do that specific job. When a issue arises we fall back on that education/training to know how to act. Yes we can adapt if the issue is out of the norm but most working people do not literally have life and death in their hands. Doctors are trained that SSRIs should work a certain way. They are trained that we should not/can not exist. How are they supposed to do their jobs (remember life and death) if suddenly they start questioning everything they were trained in.
Write prosecutors? No law has been broken. Write doctors? That would get us as far as when people go to their own doctor and get that "I don't know." Write medical institutions? Ok Ill put aside the wrong use of the word as I think I understand what you meant. That could be a viable course of action but before could present anything we need to be able to quantify it first. Just saying "so and so feels this way" doesn't mean jack to the medical profession.
As to Kk88; would be nice in theory but sadly there is no experts. As far as doctors are trained we should not exist. People like to think that doctors don't WANT to understand us; that's just not the case. People need to stop and think that being a doctor is a job. Just like our jobs; we was educated or trained to do that specific job. When a issue arises we fall back on that education/training to know how to act. Yes we can adapt if the issue is out of the norm but most working people do not literally have life and death in their hands. Doctors are trained that SSRIs should work a certain way. They are trained that we should not/can not exist. How are they supposed to do their jobs (remember life and death) if suddenly they start questioning everything they were trained in.
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Re: PSSD In Person Meet Up Event
I live in Atlanta. I’d like to meet up with anyone on here for a beer or a cup of coffee. I’m not interested in strip clubs or protesting doctors offices..... Either reply or send a direct message.
Warren
Warren
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Re: PSSD In Person Meet Up Event
I'm in Chicago. Would be down for a conference or a meet up of sorts. Can wingman effectively but will definitely not be looking to shag because I have a pregnant girlfriend (sperms still work).
Re: PSSD In Person Meet Up Event
Did you had sex with or without meds like Viagra,cilias.How much year is you on pssd?Did you wait to get aroused?alteredhomeostasis wrote:I have a pregnant girlfriend (sperms still work).
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Re: PSSD In Person Meet Up Event
I used cialis. I've had PSSD since mid June so its about 9 months now.
I haven't really been aroused since I got pssd. I still feel some arousal when we hook up, but without any contact or initiation theres no arousal.
I haven't really been aroused since I got pssd. I still feel some arousal when we hook up, but without any contact or initiation theres no arousal.
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