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Monday, February 20, 2012
Clinical Trials Update
So at 11am this morning, we will be signing Brady up for clinical trials!!!!! These trials have shown promise at reversing cognitive and motor defects of Angelman Syndrome in a mouse model. There will be 24 participants chosen for this trial in Florida. Praying that our Brady is chosen to participate and that the trials are successful in humans as they have been in the mouse model! Please keep our family as well as, the other families and doctors/researchers in your thoughts and prayers over the next few months as this could quite possibly be the first ever Angelman Syndrome treatment :) Regardless of whether our little guy is chosen for this trial, we are super excited for everyone involved and cant wait to see what the future holds!!!!! Will keep you all posted :)

posted by angelwings @ 3:15 AM
   5 comments
5 Comments:
  • At 4:54 AM, Blogger Huub Klein said…

    Hi all, we all hope that your angel will be selected for the trial. Could you update us with the latest news?

    Big smiles from Holland.

     
  • At 11:10 PM, Blogger angelwings said…

    Hi Huub! We got into the trials!! Will keep you all posted :)

     
  • At 7:12 PM, Blogger jboy said…

    Hi there im realy happy for your little man, my little girl is 9 and has angleman im realy hoping these trials can do for humans what it did for animals.

    keep us posted
    God Bless

     
  • At 7:15 PM, Blogger jboy said…

    yes keep me posted please im realy interested to hear how you get on

     
  • At 3:30 PM, Blogger joska said…

    Hi, can you update on the trial. I know you probably must not tell anything just give us a hint of hope that you see improvement or any sign of change.
    love from us

     
 
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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.

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