Support the National Alopecia Areata Foundation

Most of you all know by now, I have alopecia areata. What? You’re bald. Yes. I’m bald.

My kids like to tell me how shiny my head is. Also, lately I have three new hairs on my head, and for some reason my right eyebrow is growing. My eyebrows were microbladed, so the hair is growing over the fake eyebrow.

When I was a kid, I didn’t talk to alopecia with anyone. In fact, if someone brought up the fact I had bald spots I would usually burst into tears or hide. I didn’t understand then that knowledge is power. Plus, I wasn’t completely bald, and I thought a good barrette or ponytail could hide my bald spots. (Pro Tip: They really couldn’t).

I found out about the National Alopecia Areata Foundation as a kid. They offer support for people with alopecias. They hold conferences yearly. I have not yet been to one. They have support groups. I have been to one of those. They also put money toward important research to find a cure for alopecia.

So this month, I’m raising money for the National Alopecia Areata Foundation. That’s right. You can click National Alopecia Areata Foundation and go right to my fundraising page. You can find out more about alopecia areata there as well! This is obviously a cause close to my heart. I would give anything to go back to little Lauren and give her some guidance on how to cope, and NAAF does just that for a lot of children with alopecia.

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