Tracy Hild.'s Comments

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At 10:35am on July 23, 2009, Cindy said…
Tracy, have you contacted NAAF for information?They have a school packet that can give to you to educate the class about Alopecia. We have never had to do this, but I do know of parents that have. I think they also have sample letters if you wanted to write a letter about Ian's alopeica to the parents so they can talk about Alopecia at home. I do suggest talking to the teacher and any school staff you feel necessary about Ian's condition. I have always contacted Sam' teacher, principal, nurse and others teachers so they are aware. Also, have you heard of the children's alopecia project? www.childrensalopeica.org. They are having their first kids conference, alopeicapalooza Aug 7-9 in PA. I know you can still register. In any event I would contact them because they maybe able to help connect you with another family in your area. They may have some good resources for you as well to help prepare Ian for school. I know this may be a stressful time for you. Sam started loosing her hair as K started. She is now going into 2nd grade and returning to school in Sept with her own short cut. I am anxious myself. Let Ian take the lead and follow his cues. Honestly, the kids at this age are only interested in playing and having fun. My daughter has never encountered a negative comment about her hair loss. How long has Ian been living with Alopeica and have you tried anything? He is very handsome anyways!!! I hope this info helps and please write back if I can help in anyway. Cindy
At 8:27am on July 23, 2009, Cindy said…
Hi Tracy, I am Cindy and a parent to a 7 yr old daughter with this condition. Welcome to AW! This is a great group of people to lean on for support and good advice. How are you and your son? Cindy
At 4:36am on July 23, 2009, Roger said…
Welcome.

Roger.
At 2:03am on July 23, 2009, Cheryl, Co-founder said…
Hi Tracy, I wanted to welcome 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.

Cheryl
At 1:53am on July 23, 2009, Pamela Rosse said…
Hello & welcome to Alopecia World, I too have AU. This is a wonderful site & everyone is so nice & helpful. So if you need to talk holler, were here.
Take Care. Hope your summer is going really well so far. Take Care & once again WELCOME!
Blessings
Pam

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