Information

Alopecia Universalis

Join today to meet, support and share information with others who are also living with all loss of hair on their bodies.

Website: http://www.AlopeciaWorld.com
Members: 851
Latest Activity: Sep 24, 2023

Discussion Forum

Stronger immune systems?

Started by Laura Adams. Last reply by Simahrya Apr 7, 2019. 43 Replies

Fingernails

Started by Stephanie. Last reply by Simahrya Apr 7, 2019. 64 Replies

alopecia univeralisis

Started by janetparsons. Last reply by Kimmbe Oct 12, 2017. 22 Replies

Comment Wall

Comment

You need to be a member of Alopecia Universalis to add comments!

Comment by Catharina on November 24, 2008 at 2:17pm
Hej! How are you all? I have had universalis since 11 years.I cannot believe how many who have Alopeci.It is really strange.We do not know if we get our lovely hair back.But the show must go on.I love to go without the wig at home but when I go to town I put it on. It takes time to accept.Now it is snow here in Sweden and cold. So I must be warm on my head!
Comment by Melissa on November 10, 2008 at 10:28pm
Hey, I just went on Cafe Press, too. There are AlopeciaWorld t-shirts, too. They say "Welcome to My World" and they are cool. I just bought a tote bag that's the outline of a bald head and the outline is the definition of alopecia. I used to go on there and buy t-shirts all the time. But now I see that they actually have a lot of alopecia gear! Who knew!?
Comment by kay kay on November 8, 2008 at 6:47pm
hi ppl
Comment by Kristin on November 8, 2008 at 6:34pm
Neat! haha I just got one too ^.^
Comment by Wayne on November 3, 2008 at 11:39am
Hello to everyone, just joined the group today. I have had AU for over 11 years and now having a place to come and chat with others who know what I am going through is a great benefit.
Comment by nrja on November 3, 2008 at 7:05am
hi ...its me nrja ..... nice to see here all my lovely frnds
Comment by claire on November 2, 2008 at 6:32pm
remember beauty is skin deep.............
Comment by Sharan on October 30, 2008 at 3:55pm
Hey Buzz, Vitiligo is a skin disease that causes loss of pigment, resulting in irregular pale patches of skin. This condition is thought to belong to the same type of auto-immune conditions as alopecia. May be you have both.
I've had alopecia nearly 23 years now. I did start AU aged 17 and traveled through AT/AA for about 15yrs. I've returned to AU and very much at peace with that.
Comment by Mari on October 23, 2008 at 12:45pm
Hey Buzz, I can't speak for anyone else but I have not lost any pigmentation. So not sure if part of it or not
Comment by Fuzzless on October 23, 2008 at 12:26pm
I've had AU for about 7 months. I miss my eyelashes the most!
 

Members (851)

 
 
 

Disclaimer

Any mention of products and services on Alopecia World is for informational purposes only; it does not imply a recommendation or endorsement by Alopecia World. Nor should any statement or representation on this site be construed as professional, medical or expert advice, or as pre-screened or endorsed by Alopecia World. Alopecia World is not responsible or liable for any of the views, opinions or conduct, online or offline, of any user or member of Alopecia World.

© 2024   Created by Alopecia World.   Powered by

Badges  |  Report an Issue  |  Terms of Service