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Sunday, June 08, 2008 |
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| Well,its been another busy night here at our house. I had to go to the funeral home,my uncle passed away. So the boys stayed with my hubby here at home,I knew they wouldn't be happy going with me. So Craig took the kiddos to his moms to eat supper. Well Brady loves to flip the dining room chairs over,hes gets a charge out of for some reason. No matter how many times we tell him,no,stop,he just keeps on. Tonight he flipped one over on his foot. My hubby said that Brady cried real tears,he knew that Brady was hurt. So I hurried home to take Brady to the ER. They done xrays and said they didn't see a break,but of course it takes days for a fracture to show up most times. Brady wasn't crying when we got there,he was laughing and totally won over the nurses,lol. Were back home now,and hes still not wanting to bare and weight on that foot. He will start to walk,then sit down and grab his foot,then butt scoots the rest of the way. Hes really cranky,so I know it must be hurting him. The doc just said it was bruised and called it a sprain,we shall see. If he isn't better by Monday we will go see the ortho doc. If things don't change,I feel like there will be more than just bruising going on. So for now,we just wait I guess. I will keep you all posted on how things go. |
posted by angelwings
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12:26 AM
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| 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.
See my complete profile
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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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