Information

Alopecia Areata

Join today to meet, support and share information and resources with others who are also living with patchy hair loss.

Website: http://www.AlopeciaWorld.com
Members: 612
Latest Activity: Jan 28, 2022

Discussion Forum

Help please

Started by hayley. Last reply by hayley Oct 17, 2018. 5 Replies

Curious about Age of AA

Started by Rayne. Last reply by BaldEagle Oct 15, 2018. 29 Replies

Comment Wall

Comment

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

Comment by Dave on September 14, 2010 at 1:11pm
They are connected, Joann, I have all of those plus I have the onset of arthritis and cataracts starting
Comment by Joanne Thomas on September 14, 2010 at 9:41am
Oh, one other thing about heredity. My doctor said that alopecia can skip a generation or generations. So it's possible that say, my great-grandmother, whom I never met, might have had it.
Comment by Joanne Thomas on September 14, 2010 at 9:39am
I was diagnosed a few years ago. One day I woke up and my part was huge - overnight! Then I got more bald spots in the back. I got cortisone shots in my head and it grew back. I worry it will start again. My hair's really thin. I have asthma and get eczema (both auto-immune) so I think they are connected.
Comment by Dawn on September 2, 2010 at 3:19am
My parents don't have AA, but auto-immune disorders (such as rheumatoid arthritis) run in both my mom and dad's side of the family.
Comment by Tish on August 27, 2010 at 5:33pm
Hi I was just diagnosed today and I'm very depressed and don't know how to cope with knowing this could happen again and again :(
Comment by Cynthia Lee Watkins on August 25, 2010 at 9:21am
Hi, Joyce, and welcome!
Comment by Joyce Marie Hawes on August 25, 2010 at 4:45am
Hello! I'd like to meet someone with this too. I've lost my hair in the year 1975. Please get back to me. Would love to have friends.
Comment by Rita on August 19, 2010 at 8:15pm
thanks cynthia!
Comment by Cynthia Lee Watkins on August 18, 2010 at 8:41pm
Welcome, Rita!
Comment by richard on August 18, 2010 at 7:48pm
amber,
not from ohio(ma actually)saw your post on the mass site also, so u r being read, some body in your area will reach out i am sure. i used this site till i found a group that meets once amonth. also made friends from san fran to maryland ,england and new zealand.
 

Members (613)

 
 
 

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