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Sunday, October 21, 2007 |
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Brady is doing really well these days,other than fighting off what we think might be an ear infection. He seems to be adjusting to his meds,finally. He has been really eating lately,and is starting to refuse the pediasure sometimes,seems its just not filling him up anymore. He has started something really cool lately,he plays with these plastic containers that doritos came in. Anyway he will go and get one of these containers,and bring it to me,to let me know hes hungry. So hes creating his own pecs,lol. Were really proud of him,and his communication skills these days,hes doing really well. We have noticed some small drop seizures in the last couple of days. He had three last night,but didnt fall to hard,so that was good. Still waiting to hear about his surgery. I will post more later. |
posted by angelwings
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10:26 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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Interactive Seizure Diary |
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Angelman
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The AS Forum was created in April
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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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