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Friday, April 29, 2005
Chance to Meet Someone Special!
I have been wanting to add something positive to Bradys blog,instead of talking about those ole seizures so I thought I would share this with you all,thought it was pretty cool.Anyway me,Brady,and Peyton went to the courthouse this week.And when we were checking out there wasn't really anyone else in there but us.The lady that was checking us out quietly asked me what was wrong with Brady,of course I was holding him and he was ugh,ugh,ughing.I wasn't offended at all,like most people might think I would be.But then she before I had a chance to really explain what he has,which I love to do,she put into telling me that someone very close to her has a son with cerebral pausy and that he couldn't do any of the things that Brady was doing.She talked about how when she seen a child that had something wrong with them,that it just touched her heart to see them doing things such as sitting up,holding things in their hands,and just having so much use for themselves,like Brady does and hes much older.She talked about how she wished that her friends child could do those things.You learn to be thankful for the little things in life,when you see or hear of something like that.Meanwhile I did tell her all about Angelman Syndrome and how he is my angel! Of course she fell in love with Brady,and Im sure she went home and told everyone that she met an angel that day!I guess my point is that I admired her for having the guts to ask me about Brady,because most people don't,and they miss out on the chance to get to know Brady,what a loss!So just remember that most people that have someone with disabilities would be glad to answer questions,rather than just have people stare at them and wonder.So don't be afraid to ask,you could learn a lot,and get the chance to meet someone very special!And just remember that if you think you have it so bad,just look around and you can always find someone that has it worse!Our family is blessed!Have a blessed day!

posted by angelwings @ 4:11 PM
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What is Angelman Syndrome?

                 

About Brady

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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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