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Thursday, February 23, 2006
Fundraiser for Angelman Organization
We are doing a fundraiser for the Angelman Organization.We are trying to raise money for the Walk-A-Thon in Birmingham on May 20. We have a sponsorship page in Brady's name.The money goes straight to the foundation.It is quick and easy to donate.About my charity: Angelman Syndrome Foundation The Angelman Syndrome Foundation seeks to improve the lives of individuals with Angelman Syndrome (AS), and their families. Through education, information exchange and support for research individuals, families, healthcare and education professionals benefit from a greater understanding of AS and improved therapies and treatment. Our ultimate goal is prevention and cure. The ASF National Walk-A-Thon brings us one step closer to realizing this dream. Thank yo uso much for your kindness. Just follow this link to view the sponship page, http://www.firstgiving.com/teambrady

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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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My Smile Can Make you Melt!!
  Like an Angel!
  What Did ya Say?
  Flash is My New Nick Name
  In Case you're Wondering....
  Wasn't me Mom!
  We Love Peyton
  Are you Talking to Me?
  Your Sooooo funny!!
  Bradys New Stacking Skill
 
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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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