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Sunday, November 20, 2005
No Seizures & New Word
Just wanted to let you all know that Brady is still seizure free so far.He is doing great!He has been seizure free for nearly 3mths now,we are so excited!He is learning in leaps and bounds.He is babbling alot more and he actually said his name this week.He was playing in the living room and was just babbling.All of the sudden he said Brady Boy,thats what we call him most of the time.I would never have believed it if someone else had not heard it as well.Anyway just thought I would let you all know how well he is doing.I will post again soon.

posted by angelwings @ 10:46 PM   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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On a Lighter Note!
  Feel free to Email Me.
  No Advertising Pease!!
  No Seizures!
  Finger in the Jet
  Look Mom I Can....
  New Room With Toys
  Oh This feels Nice
  Drinking while Swimming
  This is my Favorite
 
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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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