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Wednesday, December 26, 2007 |
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Well its been a busy Christmas! We had 3 celebrations to attend,and Brady has been sick the entire time. After two rounds of two different types of antibiotics,he still has an ear infection in both ears. His cheeks have turned bright red,so it seems he has a viral infection on top of the ear infection. We went back to the doc today and he got a strong antibiotic shot,so hopefully that will do the trick. Hes sitting here fussing as I type,he is so cranky.
Anyways Im going to post some of the Christmas pictures in his photobucket,so be sure and check out the last picture and video link on the right side of the page,to check out his pictures. Gotta go tend to him for now. Will post more later. |
posted by angelwings
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11:47 PM
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(aw, i'm sorry to hear the little guy is still sick.)
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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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Merry Christmas Comment Graphics
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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
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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(aw, i'm sorry to hear the little guy is still sick.)