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Tuesday, May 06, 2008 |
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Brady is doing well today,feeling lots better. We started the morning out by him falling off the bed,he didn't cry though,he just had a really stunned look on his face,but he was ok,lol. He teaches me something new every day. Today I learned that Hash brown Casserole will stick to the wall,lol. He thought it would be funny to slap the spoon I was feeding him with and of course it landed all over the wall :o At the moment he is harassing the poor cat,but better the cat than me! His ear seems to be totally well,but were finishing up our antibiotic. I have to brag on Peyton,he got saved this past weekend!!!!!!!!!! Im so proud of him. God has really been working on him for several weeks now. We had no idea what was going on with him,until Thursday of last week. He went to a program at church Saturday night. He went down to the alter and gave his life to Christ. He is such an amazing little boy,we truly are blessed to have two very special little boys in our family. Anyway now that I'm done bragging,I'm signing off. Will post more later. |
posted by angelwings
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10:31 PM
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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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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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