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Tuesday, June 10, 2008
Things are good here. I took Brady to the Ped today. He thinks that Brady's foot is probably just sprained,since he isn't showing constant pain. We have an appt with an orthopedic doc tomorrow. I'm not sure that we are going to take him in,he has been walking all over the place tonight,showing few signs of his foot hurting. We will see how he's doing when we get up in the morning. I will keep you guys posted on how it goes.

posted by angelwings @ 12:55 AM
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What is Angelman Syndrome?

                 

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.

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  HAPPY BIRTHDAY BRADY BOY!!!!!!!!!!!!!!!!!
 
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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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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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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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