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Sunday, June 08, 2008 |
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Well,Brady continues to have trouble with his foot. He has walked a little bit,but not more than a couple steps at the time. He is obviously favoring one foot. Were going to the doc in the morning to have it checked out again. It is possible that they are going to do a cast,since he is still having problems with it,we will know more tomorrow. The doc just said to give him til tomorrow and see if he is still not wanting to bare weight on it,then he may recommend casting.
As for his stitches,they look a lot better,the redness is gone. at least were getting to handle one problem at a time,so thats the bright side I guess,lol. Anyways,Im beat,so I will post more tomorrow,stay tuned for another episode of Days of Our Lives,lol. |
posted by angelwings
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11:04 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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HAPPY BIRTHDAY BRADY BOY!!!!!!!!!!!!!!!!!
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Interactive Seizure Diary |
This
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Angelman
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The AS Forum was created in April
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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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