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Monday, December 17, 2007 |
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Well we went to the ENT today. Brady has a major ear infection in both ears. It isn't draining,so is making him extremely dizzy and unsteady. He is still walking,but stumbling all over the place. The ENT was amazed that he could walk at all,with the shape his ears are in. So anyways,he put Brady on another antibiotic,and wants to recheck him again in 2 weeks. Its amazing how tough Brady is. He has been a bit cranky and unstable,but otherwise hes been doing well. The doctor was amazed too,he said if it were one of us and our ears looked like that,we wouldn't even be able to walk around. So we started our new antibiotic tonight,hopefully he will start getting better soon. His brother also has an ear infection as well,so he started on the same kind of antibiotic as Brady. After we were done at the doc today,I had to take big brother to the dentist,he had a cavity,his first :( But he done really well. The bad news is,his mouth is very over crowded so we now have to the the Orthodontist to either have some teeth pulled to make room,or to get braces. Our dentist did give me the name of a dentist friend out of town,that he said would be glad to see Brady. We haven't been able to find anyone that would see him,so I'm going to call this guy tomorrow,hopefully we will be able to see him soon. I hope and pray that Brady doesn't end up with braces on his teeth,like his brother.Anyways we wont worry about it now,his teeth are perfect so far,so were keeping our fingers crossed.
Oh about the allergy that they think Brady has,we really didn't find out anything today. For some reason the doc didn't want to do allergy testing on Brady. I think he was more concerned about his ears right now. So maybe when we get his ears cleared up,we can get back to the allergy tests.
Well that's about it for now,I'm ramblin,I think I'm tired,lol. I will post more later. |
posted by angelwings
@
11:07 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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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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