Missy Gal
  • Female
  • Albany Georgia
  • United States
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Missy Gal's Discussions

Knowing there are others like me.

Started this discussion. Last reply by Chi_Loss Jun 16, 2020. 3 Replies

Yes I know it's weird but this just makes me feel much better knowing there is a site that supports woman (people) like me. Most people don't know what I see when I get home and lift my hair up in…Continue

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Chi_Loss replied to Missy Gal's discussion Knowing there are others like me.
"i understand exactly how you feel. and I especially remember how it felt when I had my first really bad episode. The good news is that they are understanding this disease more and more and I expect there will be a new drug on the market in the next…"
Jun 16, 2020
Baroness replied to Missy Gal's discussion Knowing there are others like me.
"It's not weird and don't apologize for sharing.  I completely understand how you feel.  I began losing my hair years ago and it just got worse.  I shaved my head a couple of months ago and it was not an easy decision. …"
Jun 9, 2020
Cheryl, Co-founder liked Missy Gal's photo
Mar 14, 2020
Missy Gal posted photos
Mar 7, 2020
Missy Gal posted a discussion

Knowing there are others like me.

Yes I know it's weird but this just makes me feel much better knowing there is a site that supports woman (people) like me. Most people don't know what I see when I get home and lift my hair up in back and see clean big spots. It is just heart breaking. My husband don't understand and it's so hard bc although it's someone you love so much, it takes that 1 thing to set you so far apart. And for me it'my alopecia. I often feel so alone and lost without my hair and watching it just bald. I have…See More
Mar 7, 2020
Missy Gal posted a status
"Hello to all, I'm new."
Mar 2, 2020
Missy Gal is now a member of Alopecia World
Mar 1, 2020

Profile Information

Relationship Status:
Married
About Me:
My name is Missy. I am a wife and mom. I have systemic Lupus, hashimoto's, and alopecia. I have decided to join this group because I feel no one really understands how losing my hair in patches really feel. Looking for support and a smile.
Do you have alopecia?
Alopecia areata
Are you age 18 or older?
Yes - I am 18 or older

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