Adults who have grown up with alopecia

Information

Adults who have grown up with alopecia

This is a group for people who had alopecia nearly all their lives. The people who grew up with alopecia as children and still have it now as adults.

Members: 287
Latest Activity: Apr 28, 2022

Discussion Forum

Progression

Started by Donna. Last reply by Donna Mar 17, 2012. 3 Replies

Comment Wall

Comment

You need to be a member of Adults who have grown up with alopecia to add comments!

Comment by PC on February 19, 2011 at 2:10am
No I have not but i do plan to attend this year
Comment by JeffreySF on February 19, 2011 at 2:00am
Hi PC,
Have you ever been to a NAAF Conference?
As the saying goes...It will change your life forever! I know it has for me and for so many others too!
Jeffrey
Comment by PC on February 19, 2011 at 12:52am
Hello everyone i've had alopecia areata all of my childhood and abouit 8 years ago i lost all my hair. I'm still struggling with wearing a wig or just going out bald. I want to get to a point that I can go out with or without it, but I dont like to draw attention to myself . Only my husband and a few close family members have seen or even know I am bald. How do you handle the questions and stares when you are out?
Comment by nicole ferland on October 31, 2010 at 5:40pm
i was 7 months when i was digonosed with alopeca and have never had a full head of hair and i am now 18
Comment by Laura Adams on October 13, 2010 at 8:54am
Well I was sixteen when my hair fell out, AT then years later AU.
Comment by Jessica Alvarez on October 6, 2010 at 2:16am
Has anyone here who has grown up with alopecia JUST had AA withOUT ever going AT or AU?
Comment by Bald and Fabulous AKA Terri on September 17, 2010 at 7:42pm
Hello everyone, I have had alopecia since I was 8yrs old. Now Im 35yrs old. At 8 the doctors were unsure as to what I had. They figured I was just stressed. I quickly lost all my hair and had to wear a wig, and learned that kids can indeed be cruel. Most of my 20's I had hair with the odd bald patch showing up. Towards the end of my 20's to current things went downhill again. Being AU now the only time I use a razor is to clean up the patchy hair on my head. 2 week anniversary of shaving my head.
Comment by Valerie Hutcherson on September 17, 2010 at 5:40pm
Hi Everyone,
I"m new to this site and am still learning my way around. I saw the name of this group and thought, this is definitely ME. I was diagnosed with AA when I was 7. My hair fell out, grew back, fell out until about 4th grade. By middle school I had AU. It was very traumatic. My hair regrew for a bit in HS, enought for me to get a weave which prompty tore the rest out. I've worn wigs basically my whole life. I haven't had any hair growth in 20 years (i'm 40 now) and while I am ok with having AT, for the most part, I still have some insecurities. I've been married 7 years and while my hubby knows, he has never seen me without a wig. That's CRAZY. Anyway, looking forward to getting to know you all.
Comment by Tracy on July 10, 2010 at 7:39am
Hello everyone I have had Alopecia for 31 years. I grew up with from the age of 12 years of age. It started off being bald spots just above my neck then my entire back of the neck hairline went up above 2 inches. By the time I was 15 I was wearing wig pieces/extensions etc. Upon turing 22 I lost so much hair in places I had to wear a wig. It would always grow back and I could discontinue wearing anything for a while. I had a surgery at about 37 and after that I went to full A totalis. I did manage to grow back my eyelashes and pubic hair but still have not grown my hair back at all. I now wear full lace wigs all the time. I get some people looking at me strange at work when I come in with my new do but I just keep it moving and do what I need to do to get through the workdays. Isn't funny how people would talk about other people when they are not looking up to their best potential via (the people), but when I come to work well groomed, confident, working hard (the people) still have strange looks on their faces. People are just that way.
Comment by Vinichuk Oksana on July 4, 2010 at 7:53am
Hello everyone ... I'm glad that I have found this site ... I hope to find friends here ... I hope that dialogue will help me create such a project in Ukraine that would be people who live on the hair loss could feel better ...
 

Members (287)

 
 
 

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