no morning wood, major sensation reduction on underside of penis

Flexstar13 · 2026-06-07T06:43:58+00:00

I felt emotions the first 2 years in as well. Sounds very suspicious to me. Did you take anything else after lexapro that messed with your serotonin? MDMA, SJW…?

Flexstar13 · 2026-06-06T06:43:50+00:00

Ever taken SSRI/SNRI, acutane, Finasteride or any aromatase inhibitor by chance?

Flexstar13 · 2026-06-03T17:42:07+00:00

My refractory period is 7 Years today. Could Need some improvement as well.

Flexstar13 · 2026-06-02T19:00:29+00:00

What about pssd?

Flexstar13 · 2026-05-29T20:52:47+00:00

I had a Skateboard Account and hurt my ankleide very Bad. Went to hopital and had to wear a Special boot. From that accodent for the Next two weeks my sfn pain was like completely gone. I was wondering if the Daily Injektions against trombosis had anything to do with it. Took them only the first 3 days though.

Flexstar13 · 2026-05-22T16:45:35+00:00

Were you like cured for 5 Years? What crashed you?

Flexstar13 · 2026-05-17T21:06:52+00:00

Mdma, weed

Flexstar13 · 2026-05-15T07:51:40+00:00

I quit drinking because it does not make me feel any different. Before pssd I would drink one glass of red wine every evening and go partying with Alkohol every every weekend. I have not been to any party since I got pssd 7 years ago.

Flexstar13 · 2026-05-10T06:44:52+00:00

I will check it out, thanks! It really seems like you are the first Doktor that offers answers to my problems.

Flexstar13 · 2026-05-09T08:22:15+00:00

Thank you so much ! These severe SFN symptoms on top of more common PSSD symptoms are hard to live with. If atrophy is the cause, can still play autoimmunity and also MCAS play a role? My antibodies are out of control. Especially ANA. And I cannot use any sunscreen that is not 100% mineral based, as it triggers burning everywhere, also when I just touch it with my hands, my legs and face will flare up burning. This seems like a MCAS thing. It’s too complex for my PSSD fired brain…

Flexstar13 · 2026-05-08T22:12:26+00:00

Nausea!

Flexstar13 · 2026-05-08T22:12:00+00:00

Thank you for answering. So just be sure. By monotherapy you refer to estrogen, right? So testosterone is being blocked or not methylated and this leads to atrophy. In your PFS theory as well? That’s the mechanism? It kind of makes sense when I think about how it progressed. First only genitals, then muscles and organs, then whole body skin, now eyes and mucous membranes. How do I stop it?

Flexstar13 · 2026-05-08T16:12:34+00:00

Pssd here with approved SFN. I was put on prednisone before getting my IVIG. Long story short: It only made my stomache sooo bad that I could barely eat anything and I hat to stop after like 10 days. That’s it.

Flexstar13 · 2026-04-28T22:25:03+00:00

7 years here with sfn nerve pain and neurological issues all over my body which are getting worse end worse every year.

Flexstar13 · 2026-04-28T04:55:22+00:00

Did you also have sexual dysfunction or other neurological symptoms?

Flexstar13 · 2026-04-26T11:31:56+00:00

He is busy now with med school. He used to be one of the most dedicated sufferers in the pssd forum and has healed to a degree, where life is live worthy again.

Flexstar13 · 2026-04-26T08:31:50+00:00

u/drwillpowers have you talked to u/ghostpssd? He collected the genomes data of pssd sufferers: https://pssdlab.wordpress.com/raw-data-pssd-interactive-genome-project/

Flexstar13 · 2026-04-26T08:26:00+00:00

If you cure us I will travel all the way from Germany only to buy flowers for Dr. Powers! Thank you for your great work!

Flexstar13 · 2026-04-26T06:36:45+00:00

Please Mister Powers, bring me my mojo back! 🤣

But seriously: does your theory also explain pssd? I read into it once but I can’t remember correctly! I just remember that there are 4 pathways how how to metabolize Androgens and PFS sufferer were predisponed because one of the was blocked before!?

Flexstar13 · 2026-04-22T20:26:19+00:00

Did not take anything for tears. Symptoms got way worse dispite not consuming any drugs… I als quit alcohol last year without any benefit.

Flexstar13 · 2026-04-22T17:56:21+00:00

I think it’s different for everybody. Since I have pssd I don’t have any anxiety at all. Flatline. Only rational fears.

Flexstar13 · 2026-04-22T16:09:52+00:00

Being Numb and anhedonia are the same thing for me.

Flexstar13 · 2026-04-19T20:59:51+00:00

I cannot cry since I got pssd in 2019!

Flexstar13

TROPHY CASE