PFS and PSSD both ARE REAL AND THIS HELL SADLY EXISTS. This PROBLEM needs yo be adressed. We need TREATMENTS AND HOPEFULLY A CURE. WE ONLY WANT OUT BEATIFUFUL LIFES BACK. LIFE WORTH LIVING...
PSSD here since 2016 it is not rare at all one study say 1/216 having permanent erectile dysfuntion on other study say 13% or having penile sensitivity loss after treatment of SSRI
Thank you for spreading awareness! 🙏🏽 I’ve had this for 5 months now and no doctor believes me. I had to drive 3 hours to another city to get any type of care
@@OGAesthetics No, i have pssd and this shit really the same as pfs life is hell because anhedonia and emotional blunting, stated parnate, at least this helps me with depression
Thank you for talking about this issue. PFS completely changed my life, and I've had it for over a decade. The cognitive symptoms are the worst. Patients have no idea what they're risking when they take finasteride.
Thank you for covering this topic. I'm a 32 year old with PFS for the last 4 years. I went from a highly ambitious, happy, life loving person with high libido without any psychiatric history, to some one's who struggling every single day. From only 3 weeks of finasteride 1mg. Zest for life, emotions and libido are non existent. I experience it as a complete loss of androgenic drive. Not feeling depressed, but ambition is gone, looking up to people is gone, feeling lonely is gone, the desire to develop oneself is gone, the desire to make/have friends is gone. Spontaneous erections never occur anymore, there's severe numbness all over the body, especially genitally.
Im also suffering with PSSD same shit anhedonia and emotional blunting no motivation no interest no memory no cognitive functions this is impossible to survive 😢😢😢
@@theDreaming Thank you for responding. Unfortunately hormone replacement therapy (hrt) has been tried by almost every single long time PFS sufferer. I've tried many hrt regimens but nothing helps. There seems to be a problem in the signalling proteins, or the way they're being built through DNA methylation. That's the current most common hypothesis at least.
Thank you so much for speaking out about this. PFS goes far beyond just sexual symptoms, though. People can experience a myriad of symptoms, including muscle loss, facial changes, loose/thinning of skin, genital changes, peyronies disease, voice changes, chest pressure, cognitive dysfunction, slurred speech, insomnia, cracking joins, anhedonia, depression, rapid aging, digestion issues, and many others. For many, these are permanent. Our channel, Moral Medicine, features patients that have been absolutely destroyed by PFS and other iatrogenic diseases. We’re doing everything we can to spread awareness about this in hopes of one day finding a cure for those affected. If you don’t mind, please take the time to check out some of our patient testimonial videos.
I'm a post menopausal woman on testosterone therapy due to very low levels. I'm extremely sensitive to dht and my hair has been falling out. As a person who has been harmed by a benzodiazepine I researched the heck out of finasteride after my doctor mentioned it to me. I was convinced it was super rare and hadn't heard of a woman having issues so I started taking 1 mg ....developed a little insomnia and freaked and stopped it. Year later recently I tried it again cause all the hairless was making me so depressed. Well I felt like crap within 3 hrs...dizziness, lightheaded, tmj pain and headache, nausea. After just one pill. This was over q week ago and I'm still not right. I also woke with a feeling of doom the following morning. I've decided just to get off the testosterone and see what happens. I was fine without it before but once on it, it's hard to get off. Do u know of any women who have had issues? I'm thinking there is one who said it wrecked her but she never wrote me back when I asked about her symptoms. Thx!
@@terrir.7604I've spoken to several women that have had serious adverse reactions to Finasteride that have left them permanently damaged. It's extremely unfortunate and my heart goes out to them. I would like to see more women talking about this issue and going public as I'm sure it's more common than we even realize.
I had/have nearly all identical symptoms but from Lexapro. PSSD and PFS are so similar! I think this condition is more prevalent than known, most of these symptoms are “subjective” and are ignored by doctors and blame the patients and tell them it’s psychosomatic and in their head.
Thanks for covering this topic. But I don't think it's as rare as you say. There is a A LOT of denial by doctors and the medical community about pfs. Therefore, it is massively underreported and untracked overall.
@@laniakeas92How about you stop spreading misinformation about this condition already? It is a PHYSIOLOGICAL condition, not psychological. Anyone that got "cured" by treating their mental health didn't have it to begin with. People are suffering greatly from this condition and some are taking their own lives, so please shut your mouth. Btw, why there is no solid proof of this condition yet, is because sufferers are having to fund their own research. Big Pharma have literally nothing to gain from researching into this condition. It would only lead to a financial loss no matter the findings.
PFS and PSSD both ARE REAL AND THIS HELL SADLY EXISTS. This PROBLEM needs yo be adressed. We need TREATMENTS AND HOPEFULLY A CURE. WE ONLY WANT OUT BEATIFUFUL LIFES BACK. LIFE WORTH LIVING...
PSSD here since 2016 it is not rare at all one study say 1/216 having permanent erectile dysfuntion on other study say 13% or having penile sensitivity loss after treatment of SSRI
Not real
@@mexicancookie7622 it's real.
Troll!
@@mexicancookie7622 it's real
@@mexicancookie7622 troll on fina
Thank you for spreading awareness of this!
Thank you for spreading awareness! 🙏🏽 I’ve had this for 5 months now and no doctor believes me. I had to drive 3 hours to another city to get any type of care
How is it ?
Now
Thanks. I’ve had this for 13 years. Horrible.
No cure??
@@OGAesthetics No, i have pssd and this shit really the same as pfs life is hell because anhedonia and emotional blunting, stated parnate, at least this helps me with depression
thank you for acknowledging this devastating syndrome
Thank you for talking about this issue. PFS completely changed my life, and I've had it for over a decade. The cognitive symptoms are the worst.
Patients have no idea what they're risking when they take finasteride.
I have severe memory loss, no verbal fluency, cant string a sentence together…
Help
not worth the risk of taking for a relatively cosmetic thing like hair loss.....i have a relatively mild case of PFS but it was a bad move to take.
Thank you for covering this topic. I'm a 32 year old with PFS for the last 4 years. I went from a highly ambitious, happy, life loving person with high libido without any psychiatric history, to some one's who struggling every single day. From only 3 weeks of finasteride 1mg. Zest for life, emotions and libido are non existent. I experience it as a complete loss of androgenic drive. Not feeling depressed, but ambition is gone, looking up to people is gone, feeling lonely is gone, the desire to develop oneself is gone, the desire to make/have friends is gone.
Spontaneous erections never occur anymore, there's severe numbness all over the body, especially genitally.
Im also suffering with PSSD same shit anhedonia and emotional blunting no motivation no interest no memory no cognitive functions this is impossible to survive 😢😢😢
Naive to the topic here, but I wonder if hormone replacement therapy can reverse this? Since it’s lowering dht can u bump testosterone back up?
@@theDreaming Thank you for responding. Unfortunately hormone replacement therapy (hrt) has been tried by almost every single long time PFS sufferer.
I've tried many hrt regimens but nothing helps. There seems to be a problem in the signalling proteins, or the way they're being built through DNA methylation. That's the current most common hypothesis at least.
Heard. Thank you for the explanation. I know you’re going to find your way with this🙏🏼
Still losing hair?
Thanks for acknowledging this horrible condition
Thank you for spreading awereness 🙏
PFS and PSSD is Real, think 100x times before do SSRI'S or Fenosteride
😳❗️Some do both ...
They are both safe
@@Moral-Medicin ah yes definitely look studies
@@minepolz320 glad you agree with me
Thank you so much for speaking out about this. PFS goes far beyond just sexual symptoms, though. People can experience a myriad of symptoms, including muscle loss, facial changes, loose/thinning of skin, genital changes, peyronies disease, voice changes, chest pressure, cognitive dysfunction, slurred speech, insomnia, cracking joins, anhedonia, depression, rapid aging, digestion issues, and many others. For many, these are permanent.
Our channel, Moral Medicine, features patients that have been absolutely destroyed by PFS and other iatrogenic diseases. We’re doing everything we can to spread awareness about this in hopes of one day finding a cure for those affected. If you don’t mind, please take the time to check out some of our patient testimonial videos.
I'm a post menopausal woman on testosterone therapy due to very low levels. I'm extremely sensitive to dht and my hair has been falling out. As a person who has been harmed by a benzodiazepine I researched the heck out of finasteride after my doctor mentioned it to me. I was convinced it was super rare and hadn't heard of a woman having issues so I started taking 1 mg ....developed a little insomnia and freaked and stopped it. Year later recently I tried it again cause all the hairless was making me so depressed. Well I felt like crap within 3 hrs...dizziness, lightheaded, tmj pain and headache, nausea. After just one pill. This was over q week ago and I'm still not right. I also woke with a feeling of doom the following morning. I've decided just to get off the testosterone and see what happens. I was fine without it before but once on it, it's hard to get off. Do u know of any women who have had issues? I'm thinking there is one who said it wrecked her but she never wrote me back when I asked about her symptoms. Thx!
@@terrir.7604I've spoken to several women that have had serious adverse reactions to Finasteride that have left them permanently damaged. It's extremely unfortunate and my heart goes out to them. I would like to see more women talking about this issue and going public as I'm sure it's more common than we even realize.
@@terrir.7604hello yeah have I talked to multiple women who got messed up from finasteride
Please make a video about PSSD (Post ssri s3xual dysfunction)
Thank you for listing the amount of side effects that are often swept under the rug. Can you talk about PSSD?
Yes, Ill get a video done soon
@@davesrx thank you so much!
thanks for speaking out!
this syndrome is not as rare as you think...just watch the comments below the video and you will see...i have this too...
Every person I have spoken to got side affects. Blocking a hormone conversion sounds like ludicrous.
this is real! thanks man
I had/have nearly all identical symptoms but from Lexapro. PSSD and PFS are so similar! I think this condition is more prevalent than known, most of these symptoms are “subjective” and are ignored by doctors and blame the patients and tell them it’s psychosomatic and in their head.
I got PSSD from this shit i don't know how to live like that
Which is insane given all the chemical pathways it changes
Thanks for covering this topic. But I don't think it's as rare as you say. There is a A LOT of denial by doctors and the medical community about pfs. Therefore, it is massively underreported and untracked overall.
@@laniakeas92 I would just like to clarify that I have never called myself a doctor in any of my videos. I am a pharmacist and I am proud to be one.
@@laniakeas92How about you stop spreading misinformation about this condition already? It is a PHYSIOLOGICAL condition, not psychological. Anyone that got "cured" by treating their mental health didn't have it to begin with.
People are suffering greatly from this condition and some are taking their own lives, so please shut your mouth.
Btw, why there is no solid proof of this condition yet, is because sufferers are having to fund their own research. Big Pharma have literally nothing to gain from researching into this condition. It would only lead to a financial loss no matter the findings.
@@davesrxo
this also happens with accutane
and with antidepressants
i'll just say that the same people who developed Finasteride also helped develop the covid vaccines and push covid related products.... Merck
Omg i cant even sleep been taking this pill for sometime now.
Hard flaccid caused by PFS or PSSD.
Please make a video on pssd too
:(
I’ve had this horrendous condition for 8 years.
:(
No real
@@mexicancookie7622 Real
great video except i'd question the 'very rare' statement. Given the sensitivity of the topic i reckon there are many unreported cases.
I look at my hair, and i wish i had took it. Because for those who describing PFS.. i feel worse already because of my bald head.
Why is it that every expert I hear talking about Finasteride is bald??
They’re coping because life sucks for most bald men. That’s why they want finasteride gone. Misery loves company. Straight losers.
1 in 100 risk is not rare, it's common.
It’s not real
@@mexicancookie7622 it's real
Finasteride is a terrible disgusting drug
It’s the best drug ever. You should get on it.
@@mexicancookie7622agreed. I love it.
@@mexicancookie7622
Completely agree with you
Best drug ever, cheap and reliable.
It should be banned from the market
@@hfud11
Why are you selfish?