Click Here to Read Brady's Story
Friday, March 17, 2006
Update on Fundrasing for the ASF
I just wanted to let everyone know that so far we have raised $660.00 on Bradys sponsorship page for the Angelman Syndrome Foundation.We would like to thank those of you who have been helping in our fundraising efforts!This money will go to the foundation and will help to fund research and promote Angelman Awareness.For those of you who do not have the link,it is, http://www.firstgiving.com/teambrady Thanks again so much for all of your support!

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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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Hello! My name is Alyssa
  Hi my name is Savannah
  My name is Macie
  Hi,Im Meagan!I am also one of Brady's Angel friend...
  Here is Kean
  Katie
  Big Buba at the Lake
  Sleeping Again!
  Here is Big Buba Sleeping
  All at the Beach
 
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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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