Click Here to Read Brady's Story
Sunday, February 26, 2006
This is Zac!
This is Zac,he is one of our angel friends from Canada! Posted by Picasa

posted by angelwings @ 11:39 PM
   0 comments
Have to Taste this Water!
Have to taste this water,lol Posted by Picasa

posted by angelwings @ 11:37 PM
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More Bubbles Mom!!!
More bubbles mom!!! Posted by Picasa

posted by angelwings @ 11:37 PM
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Thursday, February 23, 2006
Fundraiser for Angelman Organization
We are doing a fundraiser for the Angelman Organization.We are trying to raise money for the Walk-A-Thon in Birmingham on May 20. We have a sponsorship page in Brady's name.The money goes straight to the foundation.It is quick and easy to donate.About my charity: Angelman Syndrome Foundation The Angelman Syndrome Foundation seeks to improve the lives of individuals with Angelman Syndrome (AS), and their families. Through education, information exchange and support for research individuals, families, healthcare and education professionals benefit from a greater understanding of AS and improved therapies and treatment. Our ultimate goal is prevention and cure. The ASF National Walk-A-Thon brings us one step closer to realizing this dream. Thank yo uso much for your kindness. Just follow this link to view the sponship page, http://www.firstgiving.com/teambrady

posted by angelwings @ 8:33 AM
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Wednesday, February 15, 2006
My Smile Can Make you Melt!!
My smile can make you melt! Posted by Picasa

posted by angelwings @ 4:32 AM
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Like an Angel!
Like an Angel! Posted by Picasa

posted by angelwings @ 4:31 AM
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What Did ya Say?
What did ya say? Posted by Picasa

posted by angelwings @ 4:30 AM
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Flash is My New Nick Name
Flash is my new nick name,wonder why!Thanks Mrs.Kim Posted by Picasa

posted by angelwings @ 4:30 AM
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In Case you're Wondering....
In case your wondering,this is what i was doing at 4am! Posted by Picasa

posted by angelwings @ 4:30 AM
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Wasn't me Mom!
Wasn't me mom!Sure did taste good though! Posted by Picasa

posted by angelwings @ 1:39 AM
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Monday, February 13, 2006
We Love Peyton
We love Peyton,hes the best big brother in the world! Posted by Picasa

posted by angelwings @ 4:59 AM
   0 comments
Are you Talking to Me?
Are you talking to me mom?? Posted by Picasa

posted by angelwings @ 4:59 AM
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Your Sooooo funny!!
Your sooooo funny!! Posted by Picasa

posted by angelwings @ 4:57 AM
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Bradys New Stacking Skill
I just had to share this, I thought it was funny.Brady isnt sleeping again,no suprise. So anyway he has really learned to stack things. I gave him some plastic bowls and cups to play with tonight, he has been sitting nearly all night stacking the cups on top of one another and even stacking them in the bowls. Its such good practice and therapy for his fine motor skills. And to think, all the expensive therapy toys we have looked at and bought, here we were with these cups right under our noses the whole time,lol! He is so funny, some of the cups are disposable so he bends them,then they wont go into the other cups, and he gets so ticked off. I have had to go and bend them back out for him, other than that he has been really content.I have never seen him so focused and content before!!!Also, Brady has never been interested in tv before.He would stop and look,but move on. But today he actually watched a cartoon almost all the way through, giggling the whole time, he loved it.He even started fussing at me when the commercial came on and I tured it trying to find another cartoon,he doesnt like commercials,but hey neither do I. I have never seen him like this before. His focus seems to be getting so much better.And I also I wanted to let everyone know that he was seizure free for 5mths on the 7th.So were are going for nearly half a year seizure free on the 7th of march,so keep your fingers crossed. Anyway I just wanted to share.

posted by angelwings @ 4:45 AM
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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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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.

Angelman Forum & Chat

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.

Cure Angelman Syndrome

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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