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I love this community. It is helping me to accept my Alopecia Universalis. While I strive to get healthier in hopes of regrowing hair, I've found so many wonderful and caring people on this website who have helped me to accept the condition. I still hope that the autoimmune disease cures itself, but I'm not stressing out over it anymore.
Today, I created a vlog on doing my make-up and getting ready in the morning. I don't bother with fake eyelashes. I don't have real ones to…
ContinueAdded by Melinda on June 2, 2018 at 5:00pm — 2 Comments
I have lived with alopecia universalis for 9 years now. Yikes! All of my thirties were bald! In this video, I share some of the challenges that being bald can have that most people don't know about or even think about.
First and foremost, let's talk about wigs. If you have more than one, people will notice,…
ContinueAdded by Melinda on May 8, 2018 at 9:30am — No Comments
I loved swimming. I was a swimmer and as an adult, I taught swimming classes. I was great at it. Then I started losing my hair. I went bald really quickly. I have Alopecia Universalis. For about a year, I taught swimming with a wig on. Most of the instruction was simple enough that I didn't have to demonstrate for the kids. I chose a stellar student and had him demonstrate.
I wore a really cheap artificial wig. It fooled everyone. I didn't have to deal with comments on my health. I…
ContinueAdded by Melinda on May 7, 2018 at 5:00am — 27 Comments
I'm going on my 9th year with Alopecia Universalis. I struggled with this for years. I decided that I was going to heal it naturally with diet and exercise because the medications that were being prescribed for me were interacting with my epilepsy medication.
I started out with a raw vegan diet and lots of juicing. It really didn't do much for me. I loved fresh juices and they tasted great, but I lost weight. That was about it. I also looked a bit too thin.
The next diet I…
ContinueAdded by Melinda on April 6, 2018 at 2:21pm — 5 Comments
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