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Mark S. Hansen has not received any gifts yet
Posted on September 13, 2017 at 3:36pm 0 Comments 0 Likes
I have had Alopecia Universalis for 45+ years. While anything is possible, I have heard more so called cure claims than I can remember. The only thing predictable about this condition is its complete unpredictability, unless you have it to my extreme. I took Prednisone, as prescribed by a dermatologist not an endrocronologist, way back the late 60's and almost all my hair came back, for about a month. When I stopped taking it, like our standard doctor told me to, because of all its side…
ContinuePosted on October 31, 2012 at 4:00pm 14 Comments 0 Likes
I have rarely considered myself a man of few words. But in this case I will. I have had alopecia totalis for over 40 yrs; no hair anywhere. And even though I have grown up, much of the world has not. I know that if I had to do it all over, I would probably made a much better go of my life, despite my condition. But no man is an island. We are all social beings and what people say to us, both to our face, and behind our back, when they think we cannot hear, permeates into us and our…
Continueif you'd ever like to talk, please feel free to send me a message. im a 21 year old college student who's had AA since i was 3 years old. i've read several of your posts and felt the urge to re - join this site and send you a message.
i am also on twitter and facebook as well. cheers :)
There are several articles on the new research below. Search online.
Hello Mark- I just read your post on Jen's discussion regarding coping with the alopecia. I was surprised to see that you are from Milwaukee; I live in the Madison area and had actually been contacted by a young teen girl in this group during the summer but was thinking we were the only ones from Wisconsin. (I was very sorry to see that you're part of the unemployed population...a hard journey to take; I watch CNN quite a bit, listening to the lack of self-esteem and associated depression from those who face the perpetual rejection. It would be even harder for those of us with AU.)
Many years ago I used to drive into the Waukesha area to meet with the NAAF-associated support group with a subsequent attempt to start one here in Madison but our medical advisor decided to move to the Twin Cities and my job working for the UW Hospital was becoming exhausting with mandatory weekly overtime, Since I worked at home, it allowed me to forgo the wig, a wonderful benefit.
Feel free to contact me at any time; as you'll see in my profile I'm retired so am perhaps spending too much time on the computer but am always glad to hear from fellow alopecians, especially those with universalis. (BTW, I'm originally from Wauwatosa but have not been back to Milwaukee for at least 20 years, usually just visiting my niece in Hartland.) Susan
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