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Monday, May 23, 2005 |
Brady's Birthday
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Just wanted to let everyone know that Brady turned 3yrs old on Saturday.He had a great b-day.We had him a small party down at Point A park.He really enjoyed himself.He got lots of toys and has really been enjoying himself.Anyway I cant believe that hes already 3yrs old already.Hes growing so fast and looking more and more everyday like a little boy,rather than a baby.I am going to post some birthday pictures on his blog so be sure to check them out. |
posted by angelwings
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9:14 PM
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What is Angelman Syndrome?
About Brady |
Read Brady's Story Here
I am 11yrs old and I have Angelman Syndrome. I may have this syndrome, but I dont let it hold me back. I love life and live it to the fullest every single day.
My mom says that our research organization, Foundation for Angelman Syndrome Therapeutics, is working really hard on a treatment or even a cure for me and my friends. I am thankful to have 25 words but I look forward to the day that I can carry on long conversations and talk so much that everybody has to ask me to please be quiet for a few minutes :) Anyway, mom says Im awesome and super funny and I have to agree,lol.
See my complete profile
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Angelman
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The AS Forum was created in April
2005 and provides an easy way for family members and carers of
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Cure Angelman Syndrome |
The Foundation for Angelman Syndrome Therapeutics (or FAST) is an organization of families and professionals dedicated to finding a cure for Angelman Syndrome and related disorders through the funding of an aggressive research agenda, education, and advocacy.
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