ALOPECIAPALOOZA IS COMING TO HAMILTON, OHIO!!!!

For those of you not familar, Alopeciapalooza is a camp devoted specifically to children with alopecia and their families. This will be our third time doing this and we are excited about being at Camp Campbell Gard this year.

The Children's Alopecia Project concentrates on Self-esteem, support and awareness.

To learn more please visIt ALOPECIAPALOOZA

Visit and Like us on Facebook

Don't forget our Website too!

Views: 81

Reply to This

Replies to This Discussion

Hi

I'm sure your next event will be a resounding success. Good luck with everything and even though I'm not attending I truly wish you all the best of fun!

Rosy

oh my!! I am new to this site! I sure hope this comes around again. even though my daughter had AA in 2011, it was so slight that it didn't affect her and I didn't do any real research or much about it before now. She now only has about 5% of her hair on her scalp, lost in about 4-5 months time.. We are grasping at straws, because she wasn't seeing a dermatologist regurlarly, not since she was 3 and now she is 11 almost.. Considered a new patient all over again. took forever to get her in... 

Sorry for my rant, sorta lost right now..

My point WAS.. IF this comes BACK, WE want to GO!!! ♥ it!! 

Hello RlynnSll Why don't you contact Cap as they have many get togethers and events through the year as well as alopecipalozza. It's a wonderful organisation doing the best they can to help children dealing with Alopecia. Are you doing ok??? My daughter has alopecia she was diagnosed at 12 ...she is now 23...So if I can help just let me know. Rosy

thanks, we are.. idk even what i am right now.. My grandfather just passed away last week, so I am sorta going through the motions. but things are getting better around our house - I have possibly found some potential places to get my daughter a hairpiece. our insurance will cover one if we have a prescription from her doctor, we can order online as long they accept our insurance as well. So it sounds promising, but i've found several ppl have had trouble - so idk.. they suggest a durable medical equipment provider, but i don't want her to look like she has a wig on - we are getting ready to move & i'd hate for the new kids to pick on her for it! ugh! wow, feels good to talk to someone who understands what i am talking about. my family feels for her, but they dont understand why i am hunting so hard for it, etc.thanks!

RSS

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