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Thursday, November 08, 2007 |
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Just wanted to let everyone know that we went to the GI doc today. Brady was super sweet all day,and such a good little traveler. He walked in and out of the hospital. He even went over to the elevator and pushed the down button when we got ready to leave,we were so proud of him.
Anyway the GI doc is going to do and endoscopy Nov.30th and see if he can figure out why hes having so many bowel movements and check for the ulcer and reflux.Hopefully it wont be anything serious and can be corrected with meds. They did say that if they dont find anything,they will most likely relate his symptoms to Irritable Bowel Syndrome.
Anyways thats all we know for now. I will keep everyone posted as we learn more. |
posted by angelwings
@
9:46 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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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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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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