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Tuesday, October 11, 2005
Brady's Therapy Room
Well Brady's therapy room is pretty much complete,except for a few final touches that is.He is now doing therapy in his new room and loving it.We come in,put him down and he goes straight to his new room.It is great!And not to mention,big brother Peyton,loves it just as much as Brady!Brady is doing therapy in his hot tub in his new room.I never dreamed that he would have anything like this,but with help from friends and family,determination,and hard work he has something it,thanks Rod!Anyway Im going to post some pictures of him in his room and hot tub,enjoy!

posted by angelwings @ 1:01 AM
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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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No Seizures!
  Fun Splashing Around
  Pool Pics
  Getting New Pool
  Me & buba Havin Fun
  This Water Feels Good!
  I'm Gonna Splash You!
  I'm Lovin This!
  Ate too Much!
  Chocolate Cake!
 
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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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