Alopecia World
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Journey of Chasing Aloprecia
I am 55 years and since Jan 2018, I have been losing my hair. I was diagnosis AA but last week doctor didn’t see follicles as she expected and did biopsy..... now I wait....
In the last 3 months I have progressed to 30% plus salt or baldness. I am still in active hair loss no end in sight.
I am assuming doctor is considering different diagnosis? Scaring vs non scaring ?
does this sound typical or familiar?
Thank you you for Your sharing.....
Replies to This Discussion
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Permalink Reply by Modern Show on
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I think it is our water wave human hair. I say a few reasons below.
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Permalink Reply by kimk on
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Great news .... I have Aloprecia Areata! Biopsy back! I have better news I am 40% or so bald and I am unable to cover up the loss...... So I am forced to get out and move on with my life. Btw I am not crazy and AA hasn’t made me stay in(although it did a few weeks ago and I have been sad but there are way worse things that can happen to a person) I don’t sell wigs. Please don’t post promotional stuff. But I need real life success stories so please post any pre and post wig pictures!
look at my $480 lace front Heat tolerated Synthetic.... the picture on left is a year ago and my hair ... the one on right is the new me!
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Great news .... I have Aloprecia Areata! Biopsy back! I have better news I am 40% or so bald and I am unable to cover up the loss...... So I am forced to get out and move on with my life. Btw I am not crazy and AA hasn’t made me stay in(although it did a few weeks ago and I have been sad but there are way worse things that can happen to a person) I don’t sell wigs. Please don’t post promotional stuff. But I need real life success stories so please post any pre and post wig pictures!
look at my $480 lace front Heat tolerated Synthetic.... the picture on left is a year ago and my hair ... the one on right is the new me!
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Permalink Reply by hagster on
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Looks great. Real looking front lace - which is key to finding a good wig.
btw - Modern Show (and a couple of other names she posts under) has become a real problem around here with her inappropriate posting.
I'm going to suggest that if you have a Facebook account, use it to join some fantastic groups for people with hair loss. These are closed groups - meaning whatever is posted is only seen by members of that group. They are a great bunch of gals and you'll pick up wig tips you probably never thought of, learn about good places to buy wigs at discount prices, get any questions you might have answered, and much more. Some of them are: Hair Loss Sisters, Jessica's Wig Support, HLS Buy, Sell & Trade, Jessica's Wig Spin-off, Helper Hair, and for a bit different one: Alopecia Areata Questions & Answers. I'm sure there are others, so just pick what you like.
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Your are very knowledgeable, thank you and great suggestions. I would prefer no Facebook are there any other blogs or better moderated sites?
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Permalink Reply by Melinda on
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It sounds so familiar. I was bald after about 8 months. It has been eight years for me now. I gave up on medical treatments though because they interacted with other drugs I was taking and the results weren't long lasting. I didn't want to take prednisone for the rest of my life. I decided a nice wig would be better for my health. It is so frustrating.
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