Click Here to Read Brady's Story
Thursday, September 07, 2006
One Year!
Just wanted to let eveyone know that today marks one year that Brady hasn't had a seizure! It has been such a journey getting to this point,and I wasn't sure that we would ever make it to this point. We are thrilled,but really scared at the same time.I can only hope and pray that he will make it through another year without a seizure.
Anyway just wanted to update everyone and ask you to continue prayer for our little man,that is what will keep him well!God bless you all.

posted by angelwings @ 10:01 PM   2 comments
Monday, September 04, 2006
Beating up and sliming dad!

posted by angelwings @ 3:08 AM   0 comments

posted by angelwings @ 2:57 AM   0 comments

posted by angelwings @ 2:23 AM   0 comments
HMM what is that?

posted by angelwings @ 2:20 AM   0 comments

posted by angelwings @ 2:15 AM   0 comments

posted by angelwings @ 2:13 AM   1 comments
Chewin Bubas crab net!

posted by angelwings @ 2:10 AM   0 comments


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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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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