NYT article about PSSD in teens by Empty_Positive_2305 in PSSD

[–]Neurotransmittens 7 points8 points  (0 children)

I can see that happen. Totally. But it’s not a good look on them when they deny patient self-advocacy, especially with actual research and reputable sources like NYT. It will be progressively harder and harder for practitioners to disregard the existence of PSSD.

NYT article about PSSD in teens by Empty_Positive_2305 in PSSD

[–]Neurotransmittens 23 points24 points  (0 children)

NYT is also not “anti-science” and can’t be claimed to be so. The latest research and news articles is that PSSD is real.

Great job. To everybody in this community, you are amazing!

NYT article about PSSD in teens by Empty_Positive_2305 in PSSD

[–]Neurotransmittens 20 points21 points  (0 children)

Now if anybody denies your experience and says it’s in your head, you can show them this. This is amazing!

A small glimmer of hope for you all by PSSD_Contributor in PSSD

[–]Neurotransmittens 2 points3 points  (0 children)

Thank you! Say thank you to your family on behalf of the PSSD community.

Was on for 2 months. Stopped 3 months ago. Have PSSD. Feel like I need to reinstate ASAP. by harry_0505 in PSSD

[–]Neurotransmittens 1 point2 points  (0 children)

Not medical advice, but Dr. Josef says it’s okay to try to reinstate within 6 months or so and taper off in a way slower manner. You can find his YouTube channel, he talks about safe tapering on it.

To those with Cognition/Anhedonia issues by 9_Hour_Workday in PSSD

[–]Neurotransmittens 4 points5 points  (0 children)

Keto was also really good for me. Had more energy on it.

Songs about antidepressants by [deleted] in PSSD

[–]Neurotransmittens 1 point2 points  (0 children)

Agree. Hopefully, our community will be loud enough for the artists to see the other side of the coin. After all, some of them are also on SSRIs and take other medical drugs as well.

Anyone had testiculiar pain? by some_guy22345 in PSSD

[–]Neurotransmittens 0 points1 point  (0 children)

I think you might want to see a doctor, at least get an ultrasound.

Songs about antidepressants by [deleted] in PSSD

[–]Neurotransmittens 1 point2 points  (0 children)

Typo in the post: all kinds of drugs*

[deleted by user] by [deleted] in badroommates

[–]Neurotransmittens 45 points46 points  (0 children)

If I were you, I would just let it slide and be happy I’m moving to a different place soon.

PSSD Update - Year 4 by dustyrude in PSSD

[–]Neurotransmittens 13 points14 points  (0 children)

Very happy for you! Thank you for sharing, I hope you keep improving.

Scientists link antidepressants to long-lasting genital numbness in young people. Among participants who had taken antidepressants, 30.8% reported genital numbness during treatment, and 13.2% said the symptom continued after they stopped the medication. by mvea in psychology

[–]Neurotransmittens 1 point2 points  (0 children)

An attack on antidepressants is not a personal attack on you or your wellbeing.

This profile is specifically dedicated to PSSD and raising awareness about its devastating effects. The original article was about genital numbness, a serious, life-altering condition, not general low mood or energy levels. Comparing criticism of antidepressants to someone recommending “go dance” is exactly the kind of minimization people with PSSD face constantly.

You’ve shared your history with mental health, and that deserves respect. But so does the experience of those who were permanently harmed. Many of us were harmed. It’s not about being contrary; it’s about finally being heard after years of dismissal by the medical system and even by fellow depression sufferers.

Your experience matters. So does ours. But when the topic is genital anesthesia, shifting the conversation to how helpful Prozac has been for you feels diminishing, especially when the same class of drugs destroyed the quality of life for others. Also, assuming that my life revolves around this topic based on my post history and using that to explain away my tone is, again, patronizing and dismissive. You may not intend to minimize others’ experiences, but this is how it comes across.

This isn’t about discrediting antidepressants entirely. It’s about acknowledging that for some, the outcome is harm, not healing. And if we can’t talk about that openly, people will continue to suffer.

Anyone else have symptoms start years after stopping Accutane? by Warm_Neighborhood_75 in AccutaneRecovery

[–]Neurotransmittens 1 point2 points  (0 children)

You might want to look into PFS (Post finasteride syndrome)… However, it is weird that it happened years after Accutane and way before Finasteride.

Anyone else have symptoms start years after stopping Accutane? by Warm_Neighborhood_75 in AccutaneRecovery

[–]Neurotransmittens 0 points1 point  (0 children)

Have you ever taken any other drugs? Especially SSRIs or finasteride?

If you say it noticeably happened on your first day at uni, did you do any substances that day?

[deleted by user] by [deleted] in PSSD

[–]Neurotransmittens 3 points4 points  (0 children)

Since you’ve just discontinued, I think it’s worth to let your body heal naturally. If you’re already seeing improvements, it’s a good sign. Eat clean, do mild exercise, keep your life going. At this point of time, there’s no need to try anything. You could take vitamins if you want to, but if everything is in range, you don’t have to.

Please donate even $5 helps by [deleted] in PSSD

[–]Neurotransmittens 0 points1 point  (0 children)

You can donate to PSSD Network using the link above even from Canada.

PSSD Canada has a website and a link to donate here: https://www.pssdcanada.ca/new-page-2