Where acceptance is all there is!

Posted on May 29th, 2008 at 9:48am —
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<3 shawna
Yes your right he is a little cutie!!! thanks so much for the lovely message im glad that someone has looked at my page and kinda helped them, in my expieriance it is easier to grow up with alopecia I am the person i am today because of it, and i think and my friends and family have all told me im GREAT!!! haha, i dont use any treatments i havnt done for many many years but that doesnt mean you and your family shouldnt, I just personally think that i am one of the people who whatever treatmeent they use it aint gonna work i was born to be bald!! maybe i was put here to help other sufferers, i did a short film for the NHS on my expieriances, people who are newly diagnosed will be able to see it, im not sure when its going to put on but my friend clare who is a producer for bbc has just finished cutting it and she said its great and very positive (and a bit amusing) thats me though.
I will let you know and post it on here you will all be one of the first to see my screen debut and when im a superstar in hollywood and collecting my oscar you can say i know her haha somehow i dont think that will be the case but if i help one person that is better than anything (well maybe not being a superstar in hollywood) ha ha just kidding,
Give your little Hayden a big kiss and a big hug with family who care so much he will be a very happy little boy xx speak soon hopefully xx
Thank you for the comment, we appreciate that. It is good that you are on here to support your cousin Hayden and learn as much as possible, I think it is nice when the whole family is supportive. I hope Monique and Hayden are doing fine, and he is accepting his AU, he seems like a well adjusted and lively lil boy. If you or monique have any questions for me please feel free to ask. Is Monique treating Hayden AU at this time?
So sweet of you to support you loved ones. Hope you find the site helpful. You can read about my daughter. Similar in age and events to Hayden. Hopefully- together we can all comfort and inform each other. Lynn
Cheryl
co-founder
my daughter has alopecia universalis since age 4. she began to loose her hairs, at age 3.
bye