Alopecia World
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Parents of Children with Alopecia in Ottawa
Hi everyone,
I have been a member here for a couple of years. I've had AU since 1996.
My 6 year old son started losing his hair about 3 weeks ago. A Derm at CHEO confirmed yesterday that he has Alopecia. Not sure yet how much he will lose, but by the looks of it he will be either AT or AU. Most of the hair on his head has fallen out. I can't believe how fast it has gone.
So I'm just wondering if there are any other parents of kids with Alopecia in Ottawa. I've dealt with own AU for years, but now I'm in uncharted territory. I'm not sure what to do, where to start....and how to make my boy realize he's not alone.
Thanks in advance for any help!
Cate
I have been a member here for a couple of years. I've had AU since 1996.
My 6 year old son started losing his hair about 3 weeks ago. A Derm at CHEO confirmed yesterday that he has Alopecia. Not sure yet how much he will lose, but by the looks of it he will be either AT or AU. Most of the hair on his head has fallen out. I can't believe how fast it has gone.
So I'm just wondering if there are any other parents of kids with Alopecia in Ottawa. I've dealt with own AU for years, but now I'm in uncharted territory. I'm not sure what to do, where to start....and how to make my boy realize he's not alone.
Thanks in advance for any help!
Cate
Tags: Ottawa
Replies to This Discussion
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Permalink Reply by Karen Leffingwell on -
Hi Cate. We are in the US, but found a great resource. It is called "CAP"- Children's Alopecia Project. They have a website, parent chat meetings, and share great info. I got a lot of info through them when my daughter was diagnosed last year. They are also on Facebook. Good luck. Karen
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Permalink Reply by Rose Marie' on -
Hi Cate
There is a Canadian support group go to www.canaaf.org Very nice people that will be willing to help. I met some of the Canadian's involved with this group at this years Naaf conference. Give them a call.
I'm a mum of a daughter with alopecia she was diagnosed when she was 12 she is now 20, if I can pass on any help I would be happy to do so.
Catch you again soon.
Rosy -
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Permalink Reply by Tara- mother of Presley on -
You can check with the Canadian Alopecia foundation at canaaf.org. They might have some information for you.
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Permalink Reply by Jules1984 on
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We're from ottawa!! We would love to meet parents and children with alopecia. Just curious... who was the derm you saw at CHEO?? Our derm is Dr. Walker... he's the one that also confirmed for us that my daughter had alopecia areata. It would be nice if we can get to know eachother.. I've messaged you already, hope to hear from you soon!
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