hello! I just joined this site and so happy i found it. i live in fleetwood not far away at all. would love to chat!! i want to help out with Children's Alopecia Project as well did you go to the fundraiser if so would love to hear all about it. look forward to hearing from you.

Kelli:

We would love to have you anytime! Go to www.childrensalopeciaproject.org and check out the calendar and show up! We would love to know if you are coming though!

Put on your calendar Saturday, March 28th. That is the biggest fundraisier we have and it's called the Spring Spectacular. Email me you and your husbands name and address and we will get you on the invitation list, include others too if you want them invited. I will email you some info I am sending to potential spnsors and donors of silent auction items. We will have 350 people attend and hopfully will raise $40 - $50,000.

Look forward to hearing from you jefferywoytovich@yahoo.com

PS. I too went to Wilson, Class of 86

yes...I agree. I think some people have dealt with this for so long though, that they are tired of fighting. I'm already tired and it's only been a year!! lol but I am always interested in finding the common link between us ; ) I just wish I knew a long time ago how bad it could get...so i could have ordered a freedom wig back then....and I ALWAYS wonder why did it get so bad this time? Im similar to you...I had AA like 5 times...never thought nothing of it...and then, out of no where...AU. Couldnt have been stress...so Im not sure what triggered it ; ) Im here to talk anytime!

hey kelli, thanks for the warm welcome! so i see the nittany lion behind u in your default pic - penn state? my older sister graduated psu and my lil brother currently attends hehe small world, huh? anywho, yeah, this site really does help me feel less alone. i was just diagnosed last month but it's really getting easier to deal with as long as i focus on the world around me instead of obsessing over my hair! well ttyl & thanks again

<3 lia

Kelli:

I am sorry but there is nothing specific for adults. I do have a few adults with alopecia that come to our monthly meetings because it helps them being around others and helping the kids. CAP of course helps anyway we can with referring docs and general information. Please feel free to call me at 610-741-5552, I live in Wyomissing and would love to meet you and have you involved. I could also arrange a meeting with adults in this area and maybe we can start AAP (Adult Alopecia Project)? Who knows. My wife is Betsy and she too has Alopecia and her cell is 610-468-1011.

Take care,
Jeff - www.childrensalopeciaproject.org

Hi Kelli,
How are you doing today? I just thought I'd stop by and say hello.
LeslieAnn

Hi Kelli,
Wecome to Alopecia Word! You seem to have quite a story! You must be a very strong woman, and I'm excited you are hear to be a shoulder to lean on. =) Everyone here is so great! I'm glad you are a part of our family!!

Hello and welcome

Hi Kelli Good to see you on here!! :)