Hey There! I'n new also in this world. I have AA and live in GA. It's wonderful how you support your baby. AA is hard and I think is even harder for children. God Bless and your baby girl.
Me too..and now to meet people who share the same experience.
I have family in Atlanta!'WOW"
I have been so alone as we all have..for far too long.
Here at Alopecia World we now have eachother and a common thread to connect us all.
MiNA
Hi Ms. Yvette
I was looking for people of color that has experenced AA. I may be in denial. I am not sure or just dont want to face the fact. My daughter which is 10 yrs. old was diagnosed at 8 w/AA. she had this spot for about a year that grew in after about 3 month of treatment, been ok for about 11/2 years, I didnt know shedding was part of the process untill I discovered this site. what's weird is she is shedding and growing at the same time, no bald spots yet which is my main fear. she had been shedding for about 5 months, but like i said still have new hair growing in, do anyone know of this happening? Oh! I also wanted to say to you, It's great that you wear wigs for andwith your daughter. I had said if my daughter loses her hair I will also, go the miles with her.
HI YVETTE, I HAVE AU AND HAVE HAD IT OVER 10 YRS. I HAVE A 5YR OLD DAUGHTER AND FIND MYSELF CONSTANTLY CHECKING HER SCALP TO SEE IF SHE IS DEVELOPING ALOPECIA. HOW IS YOUR DAUGHTER COPING WITH ALOPECIA?
Wow, I know how hard it can be! I have had alopecia for about 30 years. After I became the spokesperson for the National Alopecia Areata Foundation, a lot of women and girls were needing my help and support, so I wrote a book called, "If Your Hair Falls Out, Keep Dancing!" It might make you and your daughter feel better! Check it out on my page -- and let me know how else I can help.
Hi Ms Yvette,
How are you and your daughter doing? Sometimes alopecia is harder on the parents than it is on the kids.
I just wanted to say hello.
LeslieAnn
Hi Ms. Yvette, I wanted to welcome you to Alopecia World. I can honestly say that we are a great community here and I hope you enjoy the time you spend with us and we look forward to your input. Cheryl, co-founder
Thank you for the friend request. My daughter went through a boat of AA and I have had Au for the past 15 years. At this point life is great and I will not allow Alopecia to become my burdens. Let her know she is not alone and feel free to contact me anytime.
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Ms. Yvette's Comments
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-Jet
I have family in Atlanta!'WOW"
I have been so alone as we all have..for far too long.
Here at Alopecia World we now have eachother and a common thread to connect us all.
MiNA
I was looking for people of color that has experenced AA. I may be in denial. I am not sure or just dont want to face the fact. My daughter which is 10 yrs. old was diagnosed at 8 w/AA. she had this spot for about a year that grew in after about 3 month of treatment, been ok for about 11/2 years, I didnt know shedding was part of the process untill I discovered this site. what's weird is she is shedding and growing at the same time, no bald spots yet which is my main fear. she had been shedding for about 5 months, but like i said still have new hair growing in, do anyone know of this happening? Oh! I also wanted to say to you, It's great that you wear wigs for andwith your daughter. I had said if my daughter loses her hair I will also, go the miles with her.
How are you and your daughter doing? Sometimes alopecia is harder on the parents than it is on the kids.
I just wanted to say hello.
LeslieAnn
Welcome to Alopecia World
Roger.
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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.