Finally Cured From Post Finasteride Syndrome

Santosh

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The cause of AIDS are anti retroviral drugs?

A big majority yes. Then party drugs make a big chunk of the rest. Malnutrition and forced vaccines too (see Africa).

Unprotected sex was never a culprit, it's all a psy op.
 

A5510

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A big majority yes. Then party drugs make a big chunk of the rest. Malnutrition and forced vaccines too (see Africa).

Unprotected sex was never a culprit, it's all a psy op.
So millions of dollars was invested and spent to finish off people with HIV? 🤣

Instead of letting nature do its job
 

Mister

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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.



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.
Miller was right about allopregnanolone. A couple of months ago a new Melcangi study showed allopreg treatment helped to normalize a lot of inflammation markers.


And as I posted pages back too, PEA Palmitoylethanolamide could help us.

Also this summary made by that user about Miller's theory is very interesting: https://forum.propeciahelp.com/uplo.../c5414badedf443eaad1fbcdc695cd340151c206a.doc
 
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Cooper

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Ranges mean nothing, we've been living in a heavy metals filled environment for the past decades, clogging hormone receptors into oblivion and not even letting a 1000ng/dl level make you feel normal.

At the same time that I'm doing my heavy metal chelation protocol, I have my T levels average 2000-3000ng/dl at any given time of the day.

Only those levels make me feel like I used to, it's delusional to think you'll feel good at 550ng/dl.

Risk of death, heart condition ... they drop above 550ng/dl if your receptors are working well.
Let how you feel dictate how much testosterone is enough, no endocrinologist on earth will know the state of your receptors and what dose is right for you.

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.
View attachment 46332

View attachment 46333

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.


One of the more well known recoveries include this lawyer from the states who few years ago received IV methylprednisolone from the Mayo Clinic.




The below is why it worked for him.

Great stuff bro, i will read it again when i have time. Btw i tried oral Methylprednisolone around 12 to 24 mg for a week i think. It didn't cause any changes on me. Maybe the dose was low? I don't know...

How this theory can relate to gut and intestines? I think many i have local auto immune reaction/ inflammation.
 

A5510

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Great stuff bro, i will read it again when i have time. Btw i tried oral Methylprednisolone around 12 to 24 mg for a week i think. It didn't cause any changes on me. Maybe the dose was low? I don't know...

How this theory can relate to gut and intestines? I think many i have local auto immune reaction/ inflammation.
You need to have autoimmune neuropathy explored with your doc. Your igg and/or ige will likely be out of range high.

It is not known what autoantibodies will be involved in our case but have a look at the below link and attached image. Long covid patients possibly have high out of range antibodies to ACE2 also.

 

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A5510

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"Artificial induction of inflammation in prostate primary epithelial cells leads to hypermethylation of the SRD5A2 promoter and silencing of SRD5A2, whereas inhibition with tumor necrosis factor α inhibitor reactivates SRD5A2 expression."
 

Mister

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"Artificial induction of inflammation in prostate primary epithelial cells leads to hypermethylation of the SRD5A2 promoter and silencing of SRD5A2, whereas inhibition with tumor necrosis factor α inhibitor reactivates SRD5A2 expression."
So what do you suggest? You recommen any supplement, herb, med, etc?
 

Mister

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Interesting new (libido) recovery from DHEA, seems to be his only side effec left from PFS after 15 years.


Damn and he tried a lot too if you go look at his member story.

Tamoxifen
HCG
Testosterone
DHT
Casodex
Cyproterone
 

Santosh

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Interesting new (libido) recovery from DHEA, seems to be his only side effec left from PFS after 15 years.


Damn and he tried a lot too if you go look at his member story.

Tamoxifen
HCG
Testosterone
DHT
Casodex
Cyproterone

I have been promoting massive DHEA dose all along ...
 

Peatfan69

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Interesting new (libido) recovery from DHEA, seems to be his only side effec left from PFS after 15 years.


Damn and he tried a lot too if you go look at his member story.

Tamoxifen
HCG
Testosterone
DHT
Casodex
Cyproterone
If he just took high doses daily instead of once a week he could probably just cure himself permanently
 

Mister

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If he just took high doses daily instead of once a week he could probably just cure himself permanently
Androhard, ultrahard, 4-andro, etc are also DHEA products right?

I've seen multiple recoveries where people used this in cycles.

Here's a recovery with dermacrine sustain aka topical DHEA (and pregnenolone I think)


@Santosh What DHEA regimen do you suggest for PFS?
 

Santosh

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Androhard, ultrahard, 4-andro, etc are also DHEA products right?

I've seen multiple recoveries where people used this in cycles.

Here's a recovery with dermacrine sustain aka topical DHEA (and pregnenolone I think)


@Santosh What DHEA regimen do you suggest for PFS?

Try high dose transdermal and high dose oral, see which works best.

High dose as in 500mg+ of either per day.
 

Peatfan69

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Androhard, ultrahard, 4-andro, etc are also DHEA products right?

I've seen multiple recoveries where people used this in cycles.

Here's a recovery with dermacrine sustain aka topical DHEA (and pregnenolone I think)


@Santosh What DHEA regimen do you suggest for PFS?

Yes - but you need high doses to really make a dent. Oral R andro (androsterone) seems is no longer available but I think a user is selling it in bulk powder on the pfs discord
 

A5510

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A PFS guy has had success with low dose naltrexone. I think he says it's the one thing that's helped him consistently over the years.

Screenshot_20230104-234325_Chrome.jpg


Key is to super low dose it as Dr Healy says here (as PFS/PSSD/PAS metabolism is messed up) so 0.25 to 0.5mg and not to be taking it if you are on psychotropic drugs.

 

Mister

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Conclusion: These data suggest that the neurosteroid androsterone contributes to the regulation of sexual function in men.
 

Mister

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Tadalafil (Cialis) Improves Lean Mass, Increases Androgen Receptor Expression and Reduces E2 Levels in Men

Conclusions: Daily tadalafil improved lean mass content in non-obese men probably via enhanced insulin secretion, estradiol reduction, and improvement of endothelial function in vivo. The in vitro increased myogenin and androgen receptor protein expression in skeletal muscle cells suggests a translational action of phosphodiesterase type-5 on this receptor.

 

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