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Thursday, March 26, 2009 |
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Check out Bradys fundraising page!
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Hey guys, as you can see, I have been making some changes to Brady's blog. I deleted the music, so that it would be more easily accessible to those of you, who are on dial up. We want everyone to have an opportunity to keep up to date on Brady's adventures, the music just makes things to slow for dial up, sorry guys.
Also, I finally got Brady's Fundraising Link listed on his blog. Just click on the symbol that says Angelman Syndrome Foundation, Donate Now, if you want to give to Brady's Fundraising page. As you can see, we ended up raising a whopping $1,521.00last year, and would love to break that record this year! Remember that 100% of the funds donated, go to the Angelman Syndrome Foundation, for research and support. So, any and all donations are welcome, big or small. Thank you guys so much for your continued support, every year! |
posted by angelwings
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12:20 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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What is Angelman Syndrome?
Just thought I would post a quick update, since Br...
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Brady at petting zoo. (1st school trip)
Brady in the news.
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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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