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Monday, February 05, 2007 |
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Update on Brady.
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Brady is doing very well since his surgery.
He isnt eating much yet,prob still sore. But hes sleeping very well! He has slept 5 nights in a row now,thats more than he has for the last year,yippppeeee!!
He has also learned to walk on the treadmill and loves it!! Hes such a big boy!
We done some color matching tonight and out of 6 times,he only got one wrong,just because he wouldnt look at it,he was bored,lol. Anyway just wanted to let everyone know how great hes doing these days.Were just so proud of the little monkey! |
posted by angelwings
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11:43 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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What is Angelman Syndrome?
Brady walking the treadmill!
We are doing two fundraisers this year,the online ...
We are doing two fundraisers this year,the online ...
We are doing two fundraisers this year,the online ...
Good news!
HMMM this treadmill is good for something!
Bradys tonsillectomy.
Waking up my best pal!
Taking the bath outside the tub!
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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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