UPDATE: wow, it's been many years unfortunately. My son is now 20 yrs old and has Alopecia universalis and my daughter was Diagnosed a couple of years ago as well and she has Alopecia Areata (similar to how her brother started). Needless to say this was tough for me intitally, I couldn't understand why this happened to both my children. However Now my Son is such a Role model and support for other kids that want to talk with him that it warms my heart. If He's Strong then I need to be. I'm still trying to be for my daughter but I am thankful she has her brother to look up to.
Hello and welcome, Angelina and Austin!
Perhaps you might like to educate Austin's school -- there's a free video tape just for that purpose available at www.naaf.org. When kids know more about alopecia, they tend to be more compassionate.
LeslieAnn
Hi, I live in St. Albert my 11 yr old daughter Kyra has Alopecia. There is a new support group in edmonton if you are interested our next meeting will be later on this month I believe. You can e-mail me at mmhart@shaw.ca or go to www.edmontonalopecia.blogspot.com but since this is a new support group the web page is not always up to date.
LeslieAnn Butler
Perhaps you might like to educate Austin's school -- there's a free video tape just for that purpose available at www.naaf.org. When kids know more about alopecia, they tend to be more compassionate.
LeslieAnn
Oct 21, 2009
LeslieAnn Butler
LeslieAnn
Oct 21, 2009
Michelle & Kyra
Jan 4, 2010