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Saturday, March 17, 2007 |
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Latest Update.
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Brady is doing really well these days. He is progressing left and right and actually sleeping more than before. He had a great week last week. He sat for the entire session of prek,in his chair and participated in all the activities. The teacher had to walk out of the room for a minute and when she came back in,Brady was still sitting in his chair waiting for her. He just giggled when she came back in,he was so proud of himself. He was supposed to pick up rubber frogs and put them into a frog container on the table. But the catch was,that he had to choose the frog over some toy rings that were placed on the table as well. He was able to choose the frogs instead of the rings,and he placed them into the container,we are so proud of him.
He also had a very good session in Pt as well. He showed more balance than ever before. He was able to right himself when he started leaning forward or backward and he took 20 independent steps during the session. He is finally getting over some of the insecurities of walking and is beginning to really enjoy the new found independence.
He has been seizure free since the one seizure at Christmas,so were very proud of that as well.
Anyway just wanted to share Brady's newest accomplishments with everyone. He is such a big boy these days, I cant believe he will turn 5yrs old in May.
Time really does fly by,they just dont stay little for long. Hugs to everyone. Will post again soon. |
posted by angelwings
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12:25 AM
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Hooray for no seizures! We will be praying for Brady to stay that way. It's such an encouragement to hear some positive things about what these Angels can accomplish. It makes me smile to read about Brady and his progress! I'm anxious to see what is coming next for our little angel, Hope. Stay in touch! Shona and the rest of the Watson tribe
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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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What is Angelman Syndrome?
Vacation photos 2/07.
Update
Update on Brady.
Brady walking the treadmill!
We are doing two fundraisers this year,the online ...
We are doing two fundraisers this year,the online ...
We are doing two fundraisers this year,the online ...
Good news!
HMMM this treadmill is good for something!
Bradys tonsillectomy.
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| Archives |
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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
Forum & Chat |
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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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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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| Angelman Links |
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Hooray for no seizures! We will be praying for Brady to stay that way. It's such an encouragement to hear some positive things about what these Angels can accomplish. It makes me smile to read about Brady and his progress! I'm anxious to see what is coming next for our little angel, Hope. Stay in touch! Shona and the rest of the Watson tribe