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Thursday, May 08, 2008 |
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Not much happening here,other than Brady being a little monkey! He has been sweet today,but pretty much a wild man. He has been picking and teasing everyone,all day long. He did do something new today tough!! He was walking towards me and noticed the broom had fallen over in front of him,he got down on his hands and feet and climbed over the broom,normally he would have just plowed over it and done his best not to fall. He is starting to actually watch where hes going,somewhat. Not much else going on here. Brady had a pretty nasty nose bleed this afternoon,I suspect it was caused from his meds,this isn't the first time this has happened. Anyway I had just put him in his car seat and looked up to see him smearing blood everywhere. So I started cleaning that up,and he starts picking at a bug bite on his leg and it is pouring blood by now. He looked like he had been beat,it was a bloody mess!! Every time I would put the rag over his nose,he would start blowing and laughing,uhhhhhhh!! But it all turned out ok,hes fine now.
Well I wont post anything else til Sunday. I'm taking Brady to the beach for the weekend,so we should have some cool pictures when we get back. Hope you all have a great weekend. I will post the pictures on Sunday. |
posted by angelwings
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10:08 PM
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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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Interactive Seizure Diary |
This
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The AS Forum was created in April
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Cure Angelman Syndrome |
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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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