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Monday, February 09, 2009 |
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Well I went for my first Wish today, it was great! I met the sweetest little boy, that really knows what he wants :) Since I was gone, Brady's dad had to take off work and take him to and from school. He was amazed because Brady walked into his classroom, turned and waved bye, pushed his dad out the door and shut the door in his face,lol lol. This is the first time that his dad has taken him to school, so it was really hard on him. He has never left Brady with anyone besides me, and he so hated to leave him. I think it made things a little easier since Brady was telling him to leave :) Brady's teacher said she could tell that he slept last night, he had a fabulous school day. It sounds like he was very cooperative. He slept all night last night and got up about 7am this morning. I on the other hand cant straighten out my sleeping habits that easy, so I was up til 5am and back up at 7am. I wish I could sleep when he sleeps, but if your not tired at the moment, it makes sleeping really hard. Anyways, Brady has had a great day. He has been in such a happy mood. He wasn't acting sleepy earlier, but is now laying next to me, going to sleep, whooo hoooo!! I am tired tonight, so guess I'm gonna get ready to hit the hay with him. I will post more later. |
posted by angelwings
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10:20 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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