Where acceptance is all there is
""Bald is beautiful" isn't just a motto for one Gilbert Middle School student— it's a lifestyle."
I recently came across this article on wxlt.com that I thought I would share with the community.
"Gracie Ann Roland was diagnosed with alopecia, a condition that causes hair loss from some or all areas of the body, a year ago."
"Rather than letting her…Continue
I been diagnosed with Alopecia universalis since 17 years old, I am 25 now and I am still the same. This year is my first year I am barley starting to feel a little more comfortable with telling people about my condition. It is extremely still hard for me to be open about it, because deep down I still feel very different from everyone else.
Added by Jazmin M. on February 19, 2018 at 6:53pm — No Comments
Hello everyone, I finally have had the courage to speak up and say I HAVE ALOPECIA! Since the age of 11 till now going to be 20. It has been emotionally painful having to loose my hair at such a young age. Also, I came to a point where I hardly came out the house because I felt really uncomfortable for everyone to notice the patches on my scalp. I have also tried and experiemnted on various different treamnets and all have failed. I have now lost more than 80% of my hair and my eyebrows…Continue
Added by Aisha on February 18, 2018 at 5:42pm — No Comments
Hi everyone! I am a new member here. Are here people who tried treatment with NAC and methyl forms of vitamins B?
I have alopecia since 2010 when I was 19. It became universalis in 2012. I never tried immunosuppressant therapy, however I know it could help if I try. But I believe that it could make things worse after treatment cancellation.
I am trying not to inhibit my immunity, but make it work on right way.
I tried different things, and last…Continue
Is there a support group in Cincinnati, Ohio?