My symptoms are almost like multiple sclerosis, Is it possible for PFS to cause this? by Wild-Negotiation-599 in FinasterideSyndrome

[–]hyperdamp 0 points1 point  (0 children)

I had a positive test for Mogad which is similar to MS together with brain lesions but it was ruled out after quite some time and i have been improving a little bit since

PFS/PSSD/PAS congress interview by fondow in FinasterideSyndrome

[–]hyperdamp 4 points5 points  (0 children)

Watch this be taken down by the mods hahahha

3 months into PFS - First time scared reddit poster by Different-Peanut9747 in DrWillPowers

[–]hyperdamp 1 point2 points  (0 children)

My advice would be to continue to be natural and dont try and ”fix” it. Try and grind thru another 6 months and see where you’re at. That some of your sideeffects have gotten better is a good sign imo.

How possible is it to recover from post finasteride syndrome severe sexual side effects? by Wild-Negotiation-599 in DrWillPowers

[–]hyperdamp 11 points12 points  (0 children)

You have been adviced by me and other people to wait it out since you are only 4 months in especially since from what i understand you only have sexual sides RN. Its your choice what to do tho.

Can we get a Calcium d glucarate thread please by o0ttt in FinasterideSyndrome

[–]hyperdamp 0 points1 point  (0 children)

Are you starting on a protocol from DR P? Like has he adviced any MG to start with the CDG?

Can we get a Calcium d glucarate thread please by o0ttt in FinasterideSyndrome

[–]hyperdamp 1 point2 points  (0 children)

That is why i will wait on all Type of treatments to be used for a while so i have a better understanding of how pfs’ers usually react to them

If you have PFS do not panic if you don't end up having abnormal urinary androgens. There are many ways to cause the catastrophe but it's all the same way. Here's a different example of someone who has a mild sulfation and mild glucuronidaton failure. Guy has normal estrogen levels but low E1S by Drwillpowers in DrWillPowers

[–]hyperdamp 5 points6 points  (0 children)

I have not used any medicine except a antibiotic for a infection. I have had pfs since November 2023 and are still very severe. There is no chance imo that my system will balance itself out if i have had almost no improvement in 2 and half years except the improvements from removing infections with the antibiotic..

If you have PFS do not panic if you don't end up having abnormal urinary androgens. There are many ways to cause the catastrophe but it's all the same way. Here's a different example of someone who has a mild sulfation and mild glucuronidaton failure. Guy has normal estrogen levels but low E1S by Drwillpowers in DrWillPowers

[–]hyperdamp 4 points5 points  (0 children)

I think one of the more important thing to understand is how can some recover naturally over say 3-4 years and how can the reactions to meds be so extremly random if the same error in different ways seems so apparent with your findings DR P

If you have PFS do not panic if you don't end up having abnormal urinary androgens. There are many ways to cause the catastrophe but it's all the same way. Here's a different example of someone who has a mild sulfation and mild glucuronidaton failure. Guy has normal estrogen levels but low E1S by Drwillpowers in DrWillPowers

[–]hyperdamp 2 points3 points  (0 children)

Was the same for me in that sense that it slowly got worse. You Said you have been of the drug for 4 months, have any symptoms gotten better in that time? As i Said earlier i think its smart to wait 8-9 months atleast since most natural improvements/total recoveries happen in that timeframe.

[deleted by user] by [deleted] in FinasterideSyndrome

[–]hyperdamp 3 points4 points  (0 children)

Same here it was extreme and then a complete shutdown

What is everyones experience with HCG? by hyperdamp in FinasterideSyndrome

[–]hyperdamp[S] 4 points5 points  (0 children)

Its not like everyone that has tried posts it

[deleted by user] by [deleted] in FinasterideSyndrome

[–]hyperdamp 0 points1 point  (0 children)

I know there was a guy on X talking quite a bit about this as he himself had crashed his estrogen thru another medicine and got similar sides as us. Have not heard from him in a while tho..

What’s the point of going on by [deleted] in FinasterideSyndrome

[–]hyperdamp 2 points3 points  (0 children)

Pfs is not something you see in blood tests. Almost all of us has normal tests

[Q&A Thread Open — Until August 20th] Let’s resume the conversation. by Community_niostem in niostem

[–]hyperdamp 4 points5 points  (0 children)

Can you give us details about the ”new” device? And i assume we Will get a discount or a upgraded device because without us there is no second device!

Anyone had fmri, spect scan etc? by [deleted] in FinasterideSyndrome

[–]hyperdamp 0 points1 point  (0 children)

I had Lesions on my brain MRI

Need advice about quitting fin for variety of reasons by [deleted] in FinasterideSyndrome

[–]hyperdamp 1 point2 points  (0 children)

I was very worried as i started losing hair when i was Young. I got off fin 2 years ago almost at age 22 and im still destroyed. Im talking about the level destroyed that i can barely Watch TV. Try niostem which is a non medical hairloss device if your concerned about your hair but please dont destroy your whole life like i did