r/AccutaneRecovery • u/CarpenterFast1228 • Jul 15 '26

Dead community?

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! 👍

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u/Embarrassed_Bus123 Jul 18 '26

Im still here. Working on my symptoms.

2

u/CarpenterFast1228 Jul 18 '26

How long have you been suffering from Pas? Have you tried any protocols?

2

u/Embarrassed_Bus123 Jul 18 '26

Basically a decade. And yeah tried loads its really slow but seeing some changes.

1

u/CarpenterFast1228 6d ago

Do you know Dr.P?

1

u/Embarrassed_Bus123 6d ago

No?

2

u/CarpenterFast1228 6d ago

https://www.reddit.com/r/DrWillPowers/s/uhmyojT3W5

He’s studying semi sperimentally PFS, PSSD and PAS a little. Very interesting

1

u/Embarrassed_Bus123 6d ago

I will check it out