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Monday, October 22, 2007 |
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| Just wanted to let everyone know that Brady is doing so well. He continues to gain new skills,seems like on a daily basis now. At the moment,he is walking around picking up things,bringing them to me,the desk is getting pretty full by now,lol. Anyway even though Brady has been walking,he hasnt been able to get himself to the standing position without pulling up on something. Anyway he started this afternoon pushing himself up on his arms,with butt in the air,and standing all the way,not holding onto anything. I think he knows he has learned a new skill,and has been practicing all night,were so proud of him. Oh we tried on Halloween costumes tonight. Brady just thought it was the funniest thing he had ever seen and done. He was strutting all over the place,once as a spider,once as stitch and once and a dinasour. Were not sure which he is going to be just yet,but you can bet which ever it is,he will be a giggling little monster,lol. Halloween,Thanks Giving and Christmas are going to be so much fun this year,since hes walking,I cant wait!! Well thats about it for now. I will post more later. |
posted by angelwings
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10:48 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
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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Angelman
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The AS Forum was created in April
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people with Angelman Syndrome (AS) to exchange information with each
other.
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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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