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Friday, March 07, 2008
Well I wish I had better news to post tonight..... Brady isnt doing so well at the moment. He has been stumbling all over the place since yesterday,and is extremely shaky today and tonight. He has been really cranky today,so something is going on. He went to sleep for about 5 minutes tonight,but had a mild seizure and is now awake. I have been suspecting seizure activity for a couple of days now,I just have that gut feeling that something is going on with him. Im wondering now if his stumbling and falling might be caused by drops,Im just not sure. He doesnt seem to be getting sick,no temp so far. Ive got our bags packed and ready to go,just in case,hopefully we wont need them. Anyways please keep our little man in your prayers. I will post more tomorrow on how hes doing. Thanks a bunch.

posted by angelwings @ 12:41 AM
   1 comments
1 Comments:
  • At 2:18 AM, Anonymous Anonymous said…

    Always trust your gut feelings, with our angels. Shelley here still checking bradys blog everyday i hope he is fine.

     
 
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What is Angelman Syndrome?

                 

About Brady

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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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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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