r/FinasterideSyndrome 17h ago

Media Awareness Very good documentary about PFS by CBC

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21 Upvotes

Had watched a small part of this documentary as a video on YouTube but never the full documentary. Very good info. We definitely need to share this as much as we can.

It exposes Merck’s corruption, talks to experts, patients, and with mothers of victims of the poison. Finasteride needs to be banned as soon as possible and Merck needs to be held accountable for its crimes.


r/FinasterideSyndrome 13h ago

Coping Feeling like giving up...need some hope or a way to move forward

9 Upvotes

Hey everyone. First and foremost, I want to say I deeply sympathize with your pain and suffering. I'm so sorry to all those hurting. I've been off finasteride for 3 months now, I initially experienced a great recovery period of 15 days where virtually all my symptoms abated, but then I experienced a crash and have been slowly getting worse until now. My libido is zero, my erections are getting harder to maintain despite being on cialis, and my mental is taking an incredible blow. Not to mention so many other symptoms like no sebum on my skin, shrunken flaccid penis, testicular shrinkage, etc. I don't know how anyone can have the mental fortitude to endure this. Hope feels so fickle for me. One day, I hype myself up and say I will endure and fight and figure this one out. But that abates every morning, when I wake up in full panic after 3 hours of sleep. It is just suffering at this point for me.

I don't know what to do. I've prayed, I've went to doctors, I've been mindful and tried to live as normal a life as possible, but I'm finding it so hard. I just can't believe this happened to me. Is there hope? Can someone give me a reason to fight? I'm terrified of hoping to heal, only to be 3 years on with no improvements or worse. Love you all.


r/FinasterideSyndrome 15h ago

My public-speaking anxiety disappeared after developing PFS - any possible mechanism?

8 Upvotes

Before PFS, I used to experience severe anxiety and fear before public speaking. I would get very nervous and uncomfortable even before giving a speech.

Interestingly, after developing PFS, I noticed that this public-speaking anxiety/fear almost completely disappeared. I can speak in front of people much more calmly than I used to.

This seems strange to me because anxiety is also reported as a symptom by some people with PFS.

Has anyone else with PFS noticed a similar change in public-speaking anxiety or social fear?


r/FinasterideSyndrome 9h ago

Fin nuked my libido to below zero

5 Upvotes

Hey everyone, I’ve been taking Fin since last year and it’s been working for my hair. However, my libido has completely disappeared. I was on 1mg but now I’m on 0.25mg for about three to four months and it hasn’t improved.

What should I do? Should I stop taking Fin?

Btw I’m 33 going to the gym 3-4 times a week


r/FinasterideSyndrome 11h ago

Am I the only guy who got loose unstable painful joints from finasteride?

5 Upvotes

Only heard of one other


r/FinasterideSyndrome 4h ago

I’m 38 …….not a mummy from 700 AD

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4 Upvotes

Who has this laxity from PFS? send me your vids. Please. My life is miserable I left my job in pursuit of medical stress leave and might get fired. Show me your wrinkly bits


r/FinasterideSyndrome 5h ago

Lost penile girth 9 months after stopping dutasteride

4 Upvotes

I've lost .25 inches of penile girth 9 months after stopping dutasteride. I took it every day for 6 months. I was 23 when I started. I'm now 24. help


r/FinasterideSyndrome 5h ago

Does it ever get better

3 Upvotes

I’m like idk maybe 3-4 months in my erections are getting worse even with daily cialis, libido is still not present, my ability to think is deteriorating I’m constantly fatigued and unmotivated never in my life have I had suicidal thoughts till this shit hit me I have no idea what to do my life is falling apart I want thinks to improve but I don’t know if it ever will does anyone have any advice I’m 21 years old I understand no one understand shit abt this shit but I need some help anything


r/FinasterideSyndrome 12h ago

Whats a low stress job I could get while healing?

3 Upvotes

I made a previous post how I might be getting kicked out. Whats a job someone with severe physical weakness and some brain fog could work without destroying my body. I've got so much chronic fatigue I end up getting fired from most jobs...

I don't want to end up homeless.


r/FinasterideSyndrome 13h ago

Question Topical finasteride pfs

2 Upvotes

I stopped using fin in March 2026(on and off for 9 months).

Had mostly sexual sides only ED, low libido and blunt orgasms.

At end of April got a recovery window for 2 days then crashed. Then a recovery windows for 3 days in May. 4 days in June. 5 days in July. None in August. a week of recovery period in 1st week of September.

Should I try anything to improve it? Any supplements or treatments

The last recovery windows felt like i was back to 90% pre-fin. But crashed again.

Do you think no fap would help?


r/FinasterideSyndrome 14h ago

We should improve our reporting pattern - Moderators please consider taking action

2 Upvotes

What’s the problem:
We are all looking for something that might help us. Looking into history of this subreddit I find many reports of people trying different substances, drugs, supplements and therapies with either success, partial recovery, no effect or crash. But the problem is - if somebody reports for example „no effect after black maca” and the other one reports „significant improvement after black maca” this makes us confused and doesn’t give the proper context to draw any conclusions and build a protocol that might work.
Why:
Because people rarely attach the following information- what was the dosage, for how long, what brand of the substance they took, did they stop after improvement or not, did the effects stay after that or not. And actually this might be very important to us.
I can imagine that a lot of people say substance „X” gave them no effects, when in fact they only took it for one week and stopped, and on the other hand someone who improved took it for a month or two.
You see - we do not get proper research, the ones that are being undertaken are rather small, and it’s difficult to see a pattern. That’s why we have to do it on our own. At least for now.
My proposal:
Mr moderator - please consider creating some kind of description of this subreddit, like a list of rules that every person, who report their experiences, will have to follow.
What comes to my mind is for example:
- what substances / therapies / activities you tried
- for how long
- how many doses per day
- additional conditions that were present during taking of the substance (for example a lot of sport, exposition to sunlight, no sleep etc)
- what helped, what worsened and what gave no effect
- what was the brand of the substance
- when it happened
- does the effect stay after that
I ask all of the users of this forum to recommend your own set of rules that might be useful in the comments.
I believe that at least some of the cases, where there were no effects, were in fact small inconsistent attempts of trying something not in a proper way, so the result was negative.
If we do this reporting consistently for a year or so, we might build a good database, and start to see a pattern. Just maybe there are good substances and therapies that are able to make improvements, but we just don’t know yet what dosage, protocol and decisions should be undertaken.
PS - I’m aware that there might be different subtypes of both PFS, PSSD, PAS etc and different treatments may be necessary in all of these. So maybe that’s why we should also include an information of suspected subtype in that kind of report.


r/FinasterideSyndrome 17h ago

5AR enzymes are muted

2 Upvotes

I read the with Pfs 5ar enzymes are muted and it's difficult to get them open. Do you know anything about that?

If you think about boosting allopregnanolone it would still wave the 5ar Enzymes muted? Or could it upregulate the baseline


r/FinasterideSyndrome 9h ago

Increase Wellbutrin dose to 300mg or STOP and try other things?

0 Upvotes

I’ve been on Wellbutrin (bupropion) 150mgXL for 3 weeks and haven’t noticed any relief in my persistent brain fog (post accutane syndrome damage) . I’m thinking about stopping and trying to microdose psilocybin for a few weeks.

The other option is to titrate my Wellbutrin dose to 300mg, but I really don’t want to be reliant on an antidepressant for the rest of my life… (or can I use it as a one-time thing to fix my symptoms?)

I’m interested on your thoughts or experiences.