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Jennifer Boucher Wilkerson has not received any gifts yet
Posted on December 16, 2010 at 9:23am 2 Comments 0 Likes
My son is complaining about his head being tender and a little puffy in another spot where he still has hair. So far he only has one patch of hair loss but I am wondering if the discomfort is normal when he's activly loosing or getting hair back.
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Sounds good. Good luck with the shots. Sam is doing one of the irritant treatments and her hair came back. Just a few small hidden spots right now. If you send me your email I will add you to my elist. You can email at cindy@childrensalopeciaproject.org. I also suggest you contact Betsy so you can get in the data base. They started doing a summer workshop for the kids 2 yrs ago. This summer it will be in Ohio at a camp ground. While the kids are engaged parents attend workshops. He may find it helpful.
If you are on FB I also just created a page for our mass group. Massachusetts CAP Kids. take care, Cindy
Hi Jennifer. How old is your son? AA is so unpredictable that it can come and go. My daughter was bald by age 6. By her 7th b-day she had hair coming back. We do a treatment that worked for her under the care of a derm at Childrens. Our meetings are held at Newton Wellsely Hospital bi monthly. I am waiting to hear back from my contact for Jan meeting date to book the room. Upton is towards Worcester. We are actually one town over from Hopkinton where the marathon starts. In Feb we are going to an interactive show at Patriots Place if that may interest you. I can send you the info. Cindy
You can get some help with the school situation from the National Alopecia Areata Foundation (www.naaf.org). They have a free "School Pack" that includes a video that the school can play for the students that explains alopecia, plus other things.
Hello and welcome, Jennifer!
How are you and your son doing today?
Leslie Ann
Hi Jennifer. Welcome to AW. My name is Cindy and I have an 8 yr old daughter. We live in Upton Ma. Where is Sunderland? If you haven't heard, there is an organization called the Childrens Alopecia Project you may want to join, no cost. I run CAP meetings here in Mass if you are ever interested in attending. How is everything? Cindy