Click Here to Read Brady's Story
Monday, February 25, 2008
Things are going well here. Brady seems to be over his sickness and were just praying he stays well for his surgery. He has been a little climbing monkey lately. He managed to use a bouncy ball to climb up and empty the top cabinets in this room. He also used a little chair to climb all the way up on the cabinets,which are as high as he is tall! He is doing really well though,still eating like a little piggy. He hasnt mastered that blue moon yet though,lol. Well I was doing laundry today and Brady decided that my piggy bank needed a diaper stuffed in it,so now I cant get it out,lol. He rearranged the bathroom and kept turning the lights off while I was trying to do laundry,its hard to do that in the dark. Anyway my little man is finally sleeping so Im going to take advantage of it,will post more later,and check back for more videos,hopefully today.

posted by angelwings @ 2:32 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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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.

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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.

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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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