www.alopeciaworld.com
Started this discussion. Last reply by hagster Jan 31, 2019. 18 Replies 0 Likes
Lisa has not received any gifts yet
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
Comment Wall (9 comments)
You need to be a member of Alopecia World to add comments!
Join Alopecia World
Thank you for your sweet words on my blog. It's been so long since I've been on here! Your kids are adorable too :) It's so nice to have other parents for support when learning about AA. It's good to meet you!
Janna
Cheryl
co-founder
My daughter Amber is also 4.5 and she was diagnosed last year. Being on this site has helped me alot and I hope that we can all to work together to build our children's self esteem as they battle this condition.