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Tuesday, December 15, 2009
Mountain Vacation Nov 2009




















posted by angelwings @ 1:46 AM
   1 comments
1 Comments:
  • At 11:46 PM, Blogger geovanna619 said…

    hi brady i just want to say your a very brave kid and a great insperation. my name is geovanna ramirez and im doing a school report on angelmans syndrome an i would like to know more about your life style my email is GeoRam619@gmail.com thank you

     
 
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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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Full update on Brady.
  Were back!!
  Well guys, its been an eventful week here, to say ...
  Well guys, in between not sleeping, we managed to ...
  Hello my friends! Not much to post about this morn...
  Cool Story/New link!
  Hey guys! Sorry I havent been posting much lately,...
  Vacation pics....
  Bradys kinder graduation
  Well we have some exciting news to share with you ...
 
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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.

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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