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Tuesday, November 20, 2007 |
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Brady has had a good day today. He hasnt been manic all day,and has even been using his words some. We had to go to the hospital and have his blood drawn,for the tests the GI doc requested. The young man that stuck him first couldnt get the vein,as Brady was moving all over the place as usual. So he had to get a woman to come and draw the blood while he helped me hold Brady. But we did get it,and Brady didnt even cry. So after that I took Brady to have his hair cut,and he was moving a lot,but done really well.
Anyways thats about it for now. Will post more later. |
posted by angelwings
@
11:25 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 |
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
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The AS Forum was created in April
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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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