Click Here to Read Brady's Story
Friday, July 15, 2011
Vote for FAST!
I added a new button so that you guys could go and vote for the Foundation for Angelman Syndrome Therapeutics (FAST)to win $1.25 million for Angelman research! We are so close to a cure, this money could be just the push that we need. I hope that you will take 30 seconds out of your day to support our cause. I pray for the day that we never have to fear losing our little man because of seizures. Please help us get there!

posted by angelwings @ 12:12 AM   0 comments
0 Comments:
 
Home        Post        Edit        Post a Comment
 


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.

See my complete profile

Home      Post        Edit
Were back!
 
  Warning: The stories that I am about to present ar...
 
  Well Brady its been a busy week in the Fore house ...
  Well its been a while folks! Sorry for all the del...
  Brady Birthday shopping and AS Walk
  Hello! Its been a little while since I posted, so ...
  Brady channel surfing and taking breathing treatment
  Hey guys!!! Just wanted to post a quick update! I'...
 
Archives
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
Angelman Blogs
All About Epilepsy