Alopecia areata awareness. January 2012.

Here is an update on my alopecia. Spread awareness and learn more about this disease on NAAF's website! This is for alopeciaworld. Please feel free to share ...

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Comment by Karli R. on January 23, 2012 at 12:58am

Here is just a quick video I put together. The whole description did not show, it should say "Please feel free to share your story in the comments or inbox me if you would like to!"
:)

Comment by Leslie Mader on January 30, 2012 at 6:40pm

Karli - i loved your video. I am truly sorry you have to go thru this. I have Alopecia Universalis now after battling areata for almost 5 yrs. I hope you have lots of love and support around you.

Leslie

Comment by Mary on January 30, 2012 at 7:05pm

Great video. Hang in there. TODAY is the 4th anniversary of the day I took back control of my life and shaved off the last of my hair. I've been mostly AU ever since, except for eyebrows and lashes returning a couple of times.

Comment by Karli R. on January 30, 2012 at 8:47pm

Thank you Leslie and Mary. I have another video on that youtube account that shows (in more detail) the loss of hair that I had last spring. I have a great deal of support. A lot of what hurts me is that I am aware of my condition, while no one else can see the spots. Sounds silly, but I think I would rather have the spots be visible to the public! In a few weeks, or possibly sooner, I will be donating at least 7 inches of it. I would rather cut it now than watch more of that long hair go to waste!! :)

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