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Thursday, February 26, 2009 |
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Just wanted to let everyone know that Brady is doing much better. He seems to have gotten over his Viral Gastroenteritis, and been nice enough to share it with his mommy and brother. But I think that we are on the mends now, his brother is going back to school tomorrow. Were considering letting Brady go back on Friday. His brother and myself didn't have nearly as bad a case as Brady did. Everything else is good here. Brady is finally up and getting into everything now. He is still sleeping a lot. He didn't sleep last night, but slept all day, til 5:30pm and is now back asleep. He is spending more time asleep, than awake these days. This crud has really taken a toll on our little guy.
Anyway just wanted to post a quick update, gotta hit the hay now. |
posted by angelwings
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1:51 AM
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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 |
This
downloadable Interactive Seizure Diary helps you track your seizure activity and medication routine. You can also record doctor appointments and notes about how you are feeling. Before a doctor appointment, print the information and share it with your physician.
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Angelman
Forum & Chat |
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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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Cure Angelman Syndrome |
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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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