12 days of POIS in a row

[LAPOISSE]

I'm a french man of 28 years old experiencing POIS for about 5 years. I found out my symptoms was correlate to ejaculation about 2 years ago and discovered the Syndrome about 6 month ago.
My symptoms are basicly :

Intense fatigue with sensation that my legs cannot support my body
Intense brain frog ; I just cannot think clearly, i'm confuse and unable to fonction in work or social context.I feel like i am 10% of my metal faculties which is very very frustrating

After seeing 10 doctors saying me it was no corelation with ejaculation and psychic fatigue, i saw a shrink who gave me SSRI (DEROXAT, molecule is paroxetine).

I was depressed and it help me a lot with my depression and with the POIS. Fort six month, I had basicly no symptoms any more but they came back with the time.

I tried to quit several time but each time, I got POIS symptoms and depression symptoms back in a very hard version. Now it's been 2 years i take it and the effect is decreasing.

Recently, I was able to control my POIS having O the friday evening in order to be OK by tuesday.

Today it's been 12th days with POIS in a row and i had an O just one time last friday.I think my POIS is getting more severe.I had some sex relation with my girl friend avoiding O but I figured maybe the control was not perfect and my libido with so high and my orgasm are so intervaled that there is some losses inside my body causing POS without O??

Anyway, I dont know what to do anymore and I'm kinda desesperated ; If I continue avoiding, I'll lose my friend and my job.I need to function at least 3 days in a week or i'm lost.

I seriously thinking about doing the Animus protocol ; I don't care about the risk, if I dont do something, i'll get crazy or worse. I just would like Animus to confirm he has since operation no more symptoms wich should lead to the fact that semen is the cause.

I believe POIS has a complicated mechanism wich may have an allergic cause and an hormonal consequence (dopamine, serotonine, testosterone, progesterone).The vitamines has some kind of action in the hormonal balance. Anyways, we need some scientific research really fast to understand that mechanism scientifically .If we are 200 or 500 persons in that forum and in NSF, it will never work out. If there is 0,01% of the male population experiencing POIS, we should be 350 000 people trying to find together a solution. I believe there is a lot of persons that experiencing our condition but doesn't know they have POIS. I needed 4 years to find out because I had sex or masturbating every day  ; Consequently it was very difficult to notice any correlation and go on internet to explore. We are 75% engineer or scientist in here, we represent just the portion fo POIS people that are trying to understand ; I believe there is so much others and maybe we should try to communicate to them.

If 100 000 persons in the world speak about POIS to their docs, maybe the will take it more seriously. Maybe we should communicate in more generalistic forum, medical forum, etc

I?m sorry if my message is confused; I?m in a very bad POIS, I?m sure you all can understand.

[0002ppdnuos]

We here genuinely know how it feels to be on POIS.
Try the remedies suggested in this forum, and get some relief if not cure.

[kurtosis]

We are 75% engineer or scientist in here, we represent just the portion fo POIS people that are trying to understand ; I believe there is so much others and maybe we should try to communicate to them.

If 100 000 persons in the world speak about POIS to their docs, maybe the will take it more seriously. Maybe we should communicate in more generalistic forum, medical forum, etc

I?m sorry if my message is confused; I?m in a very bad POIS, I?m sure you all can understand.

Hi LAPOISSE,
The problem with communicating is that other sufferers simply do not recognise they have POIS. Some just feel "under the weather". Indeed, we can't even say for certain what POIS is so it's possible that some men have had POIS like symptoms but it has been treated with testosterone, anti-depressants which greatly reduce their libido and or other treatments we can't even speculate about. POIS like symptoms can be caused by pituitary adenomas depending on which hormone is secreted.

[vetrofragile79]

Hello Lapoisse, I'm 32 years old and I suffer from pois since I was 16 years. The doctors do not recognize this disease there is nothing to do, I have also made use SSRI drugs such as citalopram and efexorr but did not improve . I was just very tired and less anxious, but without emotion. It 's been hard to stop SSRIs, but I made it, has for many years that I look for someone with the syndrome and I'm happy to be here on this forum. Never reach the 100,000 users, it is impossible . But each of us can do our best to let everyone know about this disease

[LAPOISSE]

I'm just saying if we all put a post on internet in different languages(maybe 20% of the french can read/write in english) linking ejaculation/orgasm + fatigue/cognitif symptoms to POIS and NORD donation program, maybe we get 3000 person willing to pay 10? each. I 'll do it in many forums as soon as I can.

I saw a sexologist in France who will try to convince a allergologist to launch some reserach program here, but as well, if i'm alone, there is no real interest for them.

[Daveman]

I'm just saying if we all put a post on internet in different languages(maybe 20% of the french can read/write in english) linking ejaculation/orgasm + fatigue/cognitif symptoms to POIS and NORD donation program, maybe we get 3000 person willing to pay 10? each. I 'll do it in many forums as soon as I can.

I saw a sexologist in France who will try to convince a allergologist to launch some reserach program here, but as well, if i'm alone, there is no real interest for them.

We have a French thread  also http://poiscenter.com/forums/index.php?topic=118.0

I alo want to get the description of POIS symptoms in as many languages as we can on this forum. I want to make a thread just for that.

We are getting good hits on Google now, and they will only get better “AS MORE PEOPLE START TO POST OVER HERE”.

With Observer’s article in El Mundo, we got a good number of new visitors and contributors, even if they are all not vocal.

So excellent idea.

I will open the Multi-lingual POIS SYMPTOMS Thread today or tomorrow, starting with English. Then anyone who wants can jump in and copy the symptoms into their own language.

[LAPOISSE]

OK perfect...i'll do it in French

[Daveman]

OK perfect...i'll do it in French

The new thread presenting typical symptomology for POIS has been created http://poiscenter.com/forums/index.php?topic=498.0 . The idea is to have these symptoms translated to as many other languages as possible to take advantage of Google and search engine linking… widen the exposure to as many as possible.

It is a write only thread, so any translations should be sent to Demografx or I via PM. We will get the translation posted to the thread.

[fidalgo]

I can do in portuguese...

[Daveman]

I can do in portuguese...

Send me your translation via PM and I'll post it to the thread.

Thanks.