I have the same
Same shit. I have a lot of pics with my neck changes, lypodistro in my face and old skin.
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Look at my face , i was very handsome that shit killed me
I started to loss my hair again after one year , anyone know if it’s a good sign to losing hair again?!
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@adamxx I can see the loss in your hand too, no muscle and folded skin. How long has it been ike this? I lost all of the hair on my crown over the last 3 year and there has been no improvement from any symptoms.
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Thank you man ! I have same issue on my nick too
My face got better when i started gym
I had some windows of recovery lately
I hope We can improve
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My hand i guess looked like this before fina! It been 9 months i guess
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I doubt as bad as it looks now , androgen deficient on the outside and below the thumb where males have some muscle. I’m aware of one guy who had very apparent facial changes that reversed at 2 years
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I also don’t have any stretchy skin in the back. Only in the front / side.
It would be interesting to know if we have more AR in the front than in the back (due to beard growth?).
I took a picture of my friend. He is a few years older than me, also balding but never used fin or minox. There’s a big difference, can barely pull anything at all.
His neck is about the size my neck was before PFS.
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I have an older brother and his skin is not the same as mine. Mine is much more stretchier. Especially on my arms. Some guys have it all over the body and the others just partially.
I will get in touch with my PFS doc soon for my treatment and will ask him about this one.
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It’s definitely worse. Does it hurt opening doors carrying bags etc ?
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Yes i d’ont have any problem,i can pull 30kg with each hand in the gym without any problem
My picture this week
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U look fine still got subcontaneous fat I expect. Sorry I’m not meaning to take away anything from what you’re going through. People tell me I look fine and I could punch their faces in
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I felt that.
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To all the guys who are experiencing facial changes, changes to their skin etc. - please also report these particular side effects to the relevant authorities.
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Yes i know but i hope i can get rid of this with hard work 
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Had an appointment today and reported everything
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Guess you could describe my post habits as a “Lurker”, though I want to post more now. Have many of the same issues. @Dknighten and @LazarusRy appear very similar to me. In fact, @Dknighten 's sudden worsening 5~ months in, I can especially relate to that. My doctor (who believes in PFS) says my symptoms are almost exactly Ehlers Danlos (Type II). Very scary. However, it’s a genetic disorder. No record of it occurring later in life. He believes my gene expression has been altered. The question is how we all can revert back. He described it to me as a light switch. If it can be flicked one way, it can be flicked back as well. I believe @LazarusRy also mentioned an individual who, after 2 years, had everything “turn back on”. That story gives me hope. I have global stretchy skin and fat loss, dark circles under eyes, horrible vision, Tinnitus, dry skin, hair still falling out (globally), gum loss, loose teeth, dry mouth, nail ridges, and more. Just a mess. Keeping positive though and working on several solutions. Will keep you posted. Much love to you all, my brothers. We are in this together and will beat this together!
P.S. Also have brain fog, but it’s much better now than the early days.
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I’ve drawn this conclusion myself and done some digging if it can be acquired.
I suggest you take this study and put in into sci-hub to get the whole article. Very interesting indeed. They discuss how hypermobility may be asymptomatic, but can be triggered by some environmental trigger. Also some discussion about hormones. Very interesting read.
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