Click Here to Read Brady's Story
Saturday, May 19, 2007
2007 Angelman Walk a Thon










































































































posted by angelwings @ 6:42 PM   2 comments
2 Comments:

  • At 8:40 AM, Blogger Zachary Rouleau said…

    hey guys! i think that your kodak was not set, when i was looking to the pics i thought that there was old pictures, lol!

     

  • At 10:02 AM, Blogger lil 1/2 pint said…

    (aw, i love looking at pictures of all the angels. so beautiful.)

     
 
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What is Angelman Syndrome?

                 

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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God Sent to Me an Angel
  Had to borrow this one from a fellow Angelman momm...
  Having fun at beach.
  Bradys first stitches!
  About our day!
  A day at the beach,April 2007
  Bradys therapy today.
  Brady is star of the month.
  Our blocks are in!!
  This is an essay by Soeren Palumbo who is a senior...
 
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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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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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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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