Click Here to Read Brady's Story
Sunday, August 27, 2006
Were back!
Just wanted to let you all know that things are looking good here.Brady has had mono and a broken leg all summer,but he is on the mend now.He has his cast off and is taking steps,and is actually trying to talk.He actually said "I love my buba".And this weekend he said "want mama".We are just thrilled with his progress,but he is talking our heads off now,lol.He is getting to be such a big boy now!Anyway just wanted to let you all know that hes doing so much better.I will keep you all posted on his progress.

posted by angelwings @ 8:56 PM   0 comments
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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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Brady's new Tricks
  Update on Brady
  Brady Just got out of the Hospital
  This is my friend Meagan
  Bradys Talking!
  Goal Helmet?
  Bradys Leg is Fractured
  Brady
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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.
Angelman Forum & Chat

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.
Cure Angelman Syndrome

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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