Click Here to Read Brady's Story
Saturday, December 06, 2008
Just wanted to post a quick update before I head to bed. Its been a rough week here, Peyton has been sick all week. He's on several meds for a cold and ear infection. Thank goodness Brady is well and actually sleeping tonight, for a change. Brady played his first game of basketball tonight and loved it! We lowered the goal down so that he could put the ball in all by himself, it was to cute. Everything else is running smoothly for the time being, just finished up last minute shopping. I think we just about have things ready for Christmas now,and Brady is already practicing opening :)
Well sorry for the short, boring post, but my hand is killing me and I'm ready for bed. So hope you all get some rest. Will post more soon.

posted by angelwings @ 11:28 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.

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The AS Forum was created in April 2005 and provides an easy way for family members and carers of people with Angelman Syndrome (AS) to exchange information with each other.

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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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