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Thursday, November 15, 2007 |
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Brady is doing better today. He has been awake and alert most of the day today. He is actually entertaining himself tonight,so thats unusual. He is all smiles tonight,and in the sweetest mood. He is also walking all over the place. He did the cutest thing at supper tonight!!! I was clearing the table after supper and was putting stuff in the refrigerator,when Brady came walking up and stood beside me,handing me the bag of chips that were off the table. I first thought he meant he wanted some,but took them from him,said thank you so much for helping,and put them away. He just grinned from ear to ear,he new exactly what he was doing!!! Im so proud of the little turkey,hes growing up so fast!!
Well hes got the entire box of wet wipes pulled out all over the floor,so I have to go clean those up. I will post more later. |
posted by angelwings
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12:23 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
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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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