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Thursday, January 19, 2006
JuicyFruiter
Just wanted to send out a little note to juicyfruiter for the kind comment posted on Bradys blog.I enjoyed reading your blog as well.Please feel free to come back anytime.Best of luck with your girlfriend.

posted by angelwings @ 2:42 AM   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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Snoozing in Daddy's Chair
  Daddy's not Gettin his Chair Back....
  Mom, I'm so Sleepy
  Brady's New Doc
  Check out our New Rides
  Just Chillin Out
  Here is My Cool Walker
  Let me Taste this Thing....
  Oh Thanks for the Help....
  Look mom!
 
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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.
Angelman Links
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