My employer will match my donations to the PFS foundation. I only committed to donate $20 a month at the time (I was considering $50/month and my employer will match up to $15,000/year). The PFS foundation had some trouble setting it up and said that it would be helpful if I could get an actual human to help out. I contacted the payment processor, Benevity, and they tried to contact the PFS foundation unsuccessfully who did not take their calls. But after many emails to the PFS foundation, they were unwilling to setup to receive payment from Benevity due to security concerns.
Hmm. Thatās interesting. Thanks for passing that along.
I think itās critical to be grouped in with women as well, rather than having it be perceived as something that only afflicts vain men who took risks to have artificially nice hair. In this day, itās actually considered acceptable to say that 50% of humanity is toxic because of their gender.
This should be called PES or whatever people could agree upon ā something that ruins the lives of men, women, and children equally.
Iāve always maintained that the best way to get the syndrome recognized is to stop attributing it to a drug. In doing so, we would also avoid Big Pharma interfering in research, as many have said lately. A neuroendocrine dysfunction syndrome.
Iāve always wondered how much resistance we would face if this condition wasnāt caused by pharmaceuticals. If it was just something that happened! Itās a shame that itās an undeniable fact for most of us that a drug caused it.
Interesting thought.
I think you almost need the right doctor to suffer from it. Then they will be motivated to understand exactly what it does or did to us. For all of the issues I see us dealing with it obviously seems like some sort of hormonal shift. But Im no doctor or scientist. But if it affects ejaculate size, sleep, mood, penis size, libidoā¦ And unfortunately a hormonal shift like that sounds extremely difficult to change. Not losing hope. It could be one area of our system which needs surgery to fix plus meds. But who knows. Im sorry you canāt work. Ive been lucky and am doing alright. Not 100% but pretty good.
Facts! I agree with your statement! At the end of the day, we are guessing what our problems are based on limited research (unfortunately). We need research done to realize the full set of our issues.
This is very important indeed. Others have proposed the term PEDS - Post Endocrine Disruption Syndrome. I think there is a thread about this topic.
It should be our primary goal to unite all PEDS sufferers on the same forum so that our numbers go up, and I think our admins are working towards that. This of course will be challenging since the different demographic groups experience PEDS differently and have different concerns, as others have noted. I donāt know if it would be feasible to create separate sub-forums on PH for PAS/PSSD patients, or teenagers, or womenā¦
The other thing that will be very useful for our cause, which will be helped and highlighted by including women, is to stop associating PEDS in men with erectile dysfunction primarily. This condition is first and foremost a loss of sexuality which is a lot more than ED. Those of us who are severely affected are all but asexual, which is a malaise of oneās āsoulā, not oneās sex organs.
I disagree.
Sure. I keep forgetting there is debate about this. My apologies.
P.S. I still havenāt told you my theory of emotions?
It sounds stupid. Can we go to Muskās Twitter and leave a message together? Ask him how he can safely take Propeciaļ¼
How about Joe Rogan?
At least he knows about finasteride harm.
How did he know
Steady diet of DARPA nanobots and blood boys
Also child sacrifices. One for each hair
He does sleep like 3h per night or something.
Not sure how he slept before his transplant, but one could always speculate.
Isnāt that Trump who sleeps for like 4 hours a night?
Maybe both. I read this article a couple of years ago when he slept 4 hours.
Looks like he have increased to 6 hours now though.
Try to PM himš