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Thursday, December 13, 2007 |
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Just wanted to update everyone on how the docs appt went today. As we suspected,they didnt find anything in the biposys,other than the fact that Brady has an allergy of some kind. So were going to see the allergy doc on Monday for allergy testing. The main thing that Brady drinks is pediasure,so were thinking its going to be something in the pedisaure that hes allergic to. But we will just have to wait and see what they find. I will let ya know as soon as we find out.
Im heading to be now,by some miracle,Brady is sleeping,whooo hooo!! So goodnight to everyone,looking forward to our first nights sleep in a loooooonng time.:) |
posted by angelwings
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10:23 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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Mommys sweet baby boys!!
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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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