u/CarpenterFast1228

Reading the latest research and theories that have been published about PAS I noticed how symptoms tend to be divided into two large groups:

- ED, no libido, anhedonia, other mental symptoms

- dry skin/lips, joint pain, problems healing wounds

In which of these two clusters do you find yourself?

Do any of you have symptoms of both the first and the second group?

Hi guys,

Since I am not able to receive the permissions to moderate this subreddit, I have decided to open another one in which we try together to understand the causes of this disease and its possible cures.

I invite you to unite and publicize it as much as possible in order to make it grow.
If you have some improvement to report, feel free to post and start a discussion👍

https://www.reddit.com/r/AccutaneSyndrome/s/2m1SogdBya

As the title says, I only need 7 karmas to be able to exceed the 100 threshold and apply to become an administrator of this page.

I kindly ask you to vote for this post
Thank you

I’m making this post to talk to this community about the work that Dr. Powers is doing to help PAS patients.

Until now he has focused more on Finasteride and SSRI patients who are in some ways similar and has obtained great results.

The point is that despite having formulated some theories on PAS, he has not yet had enough patients available to study this syndrome.

That is why if you have the possibility you absolutely have to perform a genetic test, a Dutch test and a series of specific blood tests to allow him to deepen our condition.

I add here a wiki link in which he explains which exams can be useful to him:

Remember that the more we are, the sooner he will be able to analyze our condition and create a cure!

Hello everyone,

As many of you may have noticed, this subreddit has been largely unmoderated lately. The current moderator has disappeared, is not responding to messages, and is not accepting new members.

To save this community, we need someone to step up and request control of the subreddit via Reddit's official process.

We are looking for a volunteer who meets the following criteria:

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Please comment below if you meet the requirements and are willing to do this, so we can support your request. Thank you!

Have there ever been cases of PSSD with substances that act on serotonin but are not real SSRIs?

I’m making this post to understand how many active members are still present within this subreddit.

I noticed that until about a year ago there were hundreds of posts a month and lots of stories of people who had followed a protocol and then recovered.

How many of you are struggling with this pathology and/or are you fighting it with some protocol?

I think that if we want to heal successfully the only way is to continue to discuss our experiences and new research in progress.

This is also why I am thinking of creating an additional whatsapp/telegram group that allows us to stay updated in real time on the evolution of the protocol we are following.

If you want to participate, please contact me! 👍

I make this post because I came into contact with both of these substances and I would like to understand which of the two caused the damage that I still have.

I don’t rule out that both contributed.

Consequently I ask you: is there any of you who used both but it’s 100% sure to had damage from only one of the two?

Do you think PAS can be treated by the approach of D.Powers?
Somebody think PFS and PAS has the exact mechanism

Good morning, I have a lot of the syntoms described in this 3d and for a long time I thought accutane caused theme.
Actually I realised I assumed in the past a supplement for prostate health
(700 mg of saw palmetto oil/day) for a couple of weeks

I had finished taking accutane about three years earlier, with some damage, although from memory they seemed less heavy than now (after 9 years in total)

Since apparently people who suffer from PAS damage have the same genetic predisposition to suffer from PFS, do you think I should consider that intake as a possible cause of harm and try to treat myself even as if I had PFS?

Or is the dose still too low to create problems?

A few days ago I started therapy with HGH starting with 2UI, I noticed benefits such as the improvement of chronic joint pain in the hands and legs, the quality of sleep, short term memory, and brain activity.

Unfortunately, however, these improvements are evident for about 6-8 hours from the injection and then gradually reduce until I inject another 2IU the day after.

What do you think? Should I try to switch to 3/4UI/ day ?

At the same time I am taking 1500mg of lithium carbonate (certified) and I have a blood concentration of 0.55-0.6.

Thanks to those who can help me.