Ok same symptoms, plus no libido and I didn’t have a problem with appetite. My symptoms were heavily cognitive, felt like I had a negative IQ. How much transdermal DHEA, how often do you take it?
Also does this effect your natural hormone output?
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Finally Cured From Post Finasteride Syndrome
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Also does this effect your natural hormone output?
Remaining is some cognitive stuff but honestly it’s all gotten better that it’s hard to tell if I even have symptoms left.
Not sure like I said, random experimentation with manganese, copper, molybdenum, thiamine.. but I wouldn’t recommend supplementing manganese or molybdenum they have their own sides and can be highly toxic supposedly
I don't think it poses too much of a problem.
I really couldn't care less, by definition if you supplement hormones it's because you don't have enough in the first place.
I am not PFS you moron. All those treatments cured other PFS people. What proof? Go to the Whatsapp PFS chat and ask them. You have no idea how many people i have helped. That is something that you can't understand. Hide your profile more, like the insecure person you are.
You are a person that deserves to be ignored. You are full of negativity as we can see from your last sentences. How old are you? You sound like a kid.
I feel silly replying to a bitter, hateful person like you. Don't reply to me. I am blocking you. Im not gonna waste my time.
This conversation is over.
Go spread your darkness somewhere else.
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Nice job martyring yourself and adding emphasis with the bold text, Shakespeare.
Unfortunately you still haven’t addressed my initial claims, which was to ask you to stop spreading your nonsenses. I am quite clear in that.
Not sure how that is “spreading darkness”, but you clearly have some sort of issue.….
Not sure how I am full of negativity as I posted clearly I made it out of PFS after a four year ordeal. That should give positivity. I simply highlighted in my “last sentences” your irrational behavior on forums and your shotgun approach to treatments. Not quite sure how that is emblematic of being a “kid”, but I’m approaching my 40s.
Anyway, onward gentlemen.
We have to be open to the fact that PFS, although being caused by a single agent, may be multifactorial in its solution and its evolution, as it causes a myriad of symptoms.
It's not out of this world to think it would cause liver and gut issues.
Some people on propeciahelp have had massive success with dry fasting.
Merry Christmas, whatever. There are 24 hours in a day.
View: https://www.reddit.com/r/IAmA/comments/jgrcj/as_requested_iama_28_year_old_female_with/?utm_source=share&utm_medium=android_app&utm_name=androidcss&utm_term=1&utm_content=share_button
^ this 'woman' has complete androgen insensitivity syndrome and is able to work which suggests lack of chronic fatigue, cognitive symptoms. In one of the comments under that post, she also says she has a high libido.
View: https://youtu.be/5vDVUPjBJiM
^ ^ she says she doesn't get armpit hair or body odour.
There’s a PSSD woman in a group chat I’m in who says she still grows body hair and still has body odor post PSSD (in fact she says she has more body hair) suggesting that PSSD may not be androgen insensitivity
One of the first SSRIs (Zimelidine) was pulled off the market for causing a recognised autoimmune condition (Guillain–Barré syndrome) of which its symptoms seem similar (but more severe) to those of PSSD.
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To be honest Androgen Receptor theory is not valid for %80 of the cases i've seen. Resulted of more damage and waste of years for me.
I tested it myself with blasting Test E. 500mg. Other guy that recommended it to me, recovered with it.
I didn't respond to the protocol. The guy had more sytemis androgenic issues like libido loss and clinical depression etc. I didn't have those. I explained all the little details and reasons of this in this thread, multiple times, if you wanna check it.
This diseases are mostly gut and auto immune related. For example another guy i know recovered %75 from PFS by juicing carrots, beets and apples daily.
Get tested for your gut first. High chance that it will show SIBO, Dybiosis and Inflammation. Those things can cause auto immune response to nearby organs by causing widespread inflammation and dysfunction. Lots of SIBO cases report sexual dysfunction as a symptom in Reddit for instance.
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I suspect PSSD and maybe PFS/PAS/long Covid is a mild form of guillain barre syndrome
Just have a look at the culprits below.
Zimelidine was one of the first SSRIs (the first in Sweden).
Some long Covid sufferers and a PSSD sufferer have noted marked improvements with the same treatments for Guillain Barre syndrome to the point where they can move on with their lives.
Wikipedia
"Guillain–Barré syndrome (GBS) is a rapid-onset muscle weakness caused by the immune system damaging the peripheral nervous system."
The penis is a muscle
I suspect the more accurate diagnosis is (mild) “chronic inflammatory demyelinating polyneuropathy” due to its potential long-lasting nature. Almost identical to Guillain–Barré syndrome but chronic as opposed to acute.
en.m.wikipedia.org
One of the more well known recoveries include this lawyer from the states who few years ago received IV methylprednisolone from the Mayo Clinic.
forum.propeciahelp.com
The below is why it worked for him.
en.m.wikipedia.org
Just have a look at the culprits below.
Zimelidine was one of the first SSRIs (the first in Sweden).
Some long Covid sufferers and a PSSD sufferer have noted marked improvements with the same treatments for Guillain Barre syndrome to the point where they can move on with their lives.
Wikipedia
"Guillain–Barré syndrome (GBS) is a rapid-onset muscle weakness caused by the immune system damaging the peripheral nervous system."
The penis is a muscle
I suspect the more accurate diagnosis is (mild) “chronic inflammatory demyelinating polyneuropathy” due to its potential long-lasting nature. Almost identical to Guillain–Barré syndrome but chronic as opposed to acute.
Chronic inflammatory demyelinating polyneuropathy - Wikipedia
One of the more well known recoveries include this lawyer from the states who few years ago received IV methylprednisolone from the Mayo Clinic.
Methyl steroids as a treatment for sexual symptoms
I’m a lawyer with 15+ years of difficult and challenging litigation experience (including 8 years for the U.S. government in Wash DC), not crazy or moronic. I’m posting here to encourage others to talk to their doctors about trying methyl steroids, which POSSIBLY totally cured my 100%...
forum.propeciahelp.com
The below is why it worked for him.
Progressive inflammatory neuropathy - Wikipedia
Attachments
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Motor unit recruitment - Wikipedia
The less motor neurons are activated, the less muscle fibres can be activated/contracted.
When you don’t use a muscle, you lose it
If something is up with the motor neurone (getting attacked) then its ability to recruit and activate as many muscle fibres as it can will be compromised.
Penile shrinkage
View attachment 46342
Motor unit recruitment - Wikipedia
The less motor neurons are activated, the less muscle fibres can be activated/contracted.
When you don’t use a muscle, you lose it
If something is up with the motor neurone (getting attacked) then its ability to recruit and activate as many muscle fibres as it can will be compromised.
Penile shrinkage
Long covid sufferers aka vaccinated people ?
Long covid isn't a thing, let's keep this topic on track and exclusively about PFS, thank you.
View: https://m.youtube.com/watch?v=h_LZSh9k-zU&feature=youtu.be
I'm also in a group chat with long Covid sufferers. Also some long Covid sufferers have seen significant recovery with BC007 which neutralises circulating autoantibodies.
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All autoimmune neuropathy. Thank me later
All linked to taking a medication :
SSRI
Propecia
Vaccine
No such thing as a virus having long term effects, let's keep it serious
HIV/AIDS?
Impotence can occur in autoimmune neuropathy.
'Alex Miller' - a proclaimed biologist who visited propeciahelp a few times (dunno if he had PFS himself) called it 23 years ago.
forum.propeciahelp.com
Research is going completely the wrong way. Baylor part 2 is flawed as they took sample sites from different areas on the genitals between PFS (base of scrotum) and controls (foreskin) before observing respective samples.
'Alex Miller' - a proclaimed biologist who visited propeciahelp a few times (dunno if he had PFS himself) called it 23 years ago.
Biologist Alex Miller - Why We Have PFS and How To Treat It
Alex Miller wrote a theory in 2009 about why we have PFS, it is believed that he too has PFS. The one thing that stood out to me was how afraid people were of his ideas and the responses he received seemed emotional and irrational. Alex presented the idea of allopregnanolone deficiency and how...
forum.propeciahelp.com
Research is going completely the wrong way. Baylor part 2 is flawed as they took sample sites from different areas on the genitals between PFS (base of scrotum) and controls (foreskin) before observing respective samples.
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The only reason people have AIDS is because they get on heavy antiretroviral meds as soon as they show HIV positive in a bloodtest.
You can show HIV positive in a bloodtest for at least 60 different reasons, one of them being being pregnant.
Again, let's be serious.
The cause of AIDS are anti retroviral drugs?
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