Recent Posts

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21
What is POIS / Re: New POIS video by member Warrior - 2023-07
« Last post by Limejuice on September 26, 2023, 08:26:55 AM »
Thanks for creating these great/informative videos!  There just isn't much content on video platforms, especially personal testimonies, and your charisma and personability add an element that a forum post can't capture.  Pretty great that the videos have 1,000 views.
22
Auto-Immune Causes and Treatments / Re: LOW DOSE NALTREXONE
« Last post by Limejuice on September 26, 2023, 08:03:02 AM »
I have tried low dose naltrexone in the past (around 2015). Unfortunately after several months of taking the medication there was no improvement to POIS symptoms.

There is a new study ongoing at the University of Chicago (in conjunction with our funded study) and they've created survey for us to complete.  It only takes 5 minutes and here's the link

https://redcap.uchicago.edu/surveys/?s=NAC9A38LJLA9HW4E
23
General POIS Discussions / full regression after stopping all my meds
« Last post by gzbking on September 26, 2023, 06:14:37 AM »
since i have stopped my meds a 8 weeks now i have full even more pois symptoms rip the good times
24
General Alternative Causes and Treatments of POIS / Re: Got Cured
« Last post by mike_sweden on September 25, 2023, 07:31:31 AM »
Shame. Shame. Shame.

You guys must investigate how much shame is rooted in POIS.
I'm ready to get into polemics with anybody about the nature of POIS.

Shame might be a factor in your POIS but don't project it onto others.

It’s usually more helpful to express opinions as personal rather than generalized  (for example, in lw’s post):

Personal:
[Shame seems to be] “rooted in my POIS”.

vs.

Generalized:
[Shame seems to be] “rooted in POIS”.

True
25
Auto-Immune Causes and Treatments / Re: LOW DOSE NALTREXONE
« Last post by Frank on September 24, 2023, 07:41:21 PM »
I have just come across this video where Dr Mark Shukhman talks about treating sexual dysfunction with LDN. He discussed Post Coital Dysphoria (PCD) which has symptoms very similar to POIS.

https://ldnresearchtrust.org/dr-mark-shukhman%E2%80%99s-presentation-sexual-function-2016-ldn-conference

I hope to try this medication out.
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Thank you very much!
27
Hi Andre,

I see from your post at https://poiscenter.com/forums/index.php?topic=4400.msg47288#msg47288 that you have found an Italian doctor in Rome who receives patients with POIS.  If this doctor wants to be listed here on our POIS Doctors list, please send me his name and information. 

Thanks !
28
I have secondary pois at the age of 20 but the thing is i had an autoimmune syndrome before. Its GBS in 2017. Maybe autoimmune diseases causes pois.
29
General POIS Discussions / Re: Free Flow Discussion about POIS
« Last post by Luciferaspois on September 24, 2023, 06:26:41 AM »
I have a question guys.
Is this Pois like life threatening or dangerous?
Finally made an account here though. Happy to be the part of community. 😊
30
General POIS Discussions / My case and some questions regarding this pois
« Last post by Luciferaspois on September 24, 2023, 05:59:13 AM »
Hey there guys, i am luciferaspois here from asia.
My life was all good where i could O like many times and it helped me to feel relax and all for like many years until something terrible happened when i was just 20 years old.

Pois started as following symptoms back in 2020:-
Sneezing.
Speech impairment( i thought something was wrong).
Runny nose.
Confusion/brainfog.


I didn't give much a big deal to this as i thought its just a general malaise which is quite common and i was just continuosly enjoying the ride of Orgasms until 2022 when i developed new set of symptoms:-

1. Adrenal rush(it felt like i am on some weed or something making me restless for whole 2 days,felt like i am not engaged with environment)

2. Anxiety:- i get anxiety more often in pois now.

3. Sleep disturbances/insomnia:- It was terrible. The sleep disturbances made my night hell.

4. Palpitations:- started just few days ago.



So I have a question for you guys?
Is this pois really life threatening/dangerous as there are so many members here who have it for quite a long time like 40+ years, while i am all irritated within 3 years.


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