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Thursday, May 10, 2007, Sarah fainted at school. She was taken to a local ER & then transported to Phoenix Children's Hospital with a diagnosis of restrictive cardiomyopathy.  

July 5, 2007 Sarah received her new heart. However, during the transplant she suffered a massive stroke that left her paralyzed. 

Click here to read Sarah's journey.

 


 

A Small Tidbit On Sarah

Mom and Dad's picture

Hi everyone.Sarah has a sore throat, so we'll be keeping an eye on her. A couple of weeks ago on one of my errands I had someone ask me how long does it take for someone with a heart transplant to get better, I said never. I left feeling a bit sad, because it's not like Sarah had a hangnail removed and she all better, but then I have to remind myself that the only way people will have of understanding heart disease is through education.That's why the heart walk was so important to us, and it went great as you all read, it truly was an awesome experience to walk with so many people that have the same goal as we do, finding a cure for heart disease. I want to thank those of you who helped Team Sarah not only meet there goal, but surpassed it. Anyways a couple of days ago I had the pleasure of taking Sarah to see the Jonas brothers in 3-D, and of course they gave us the best seats in the theater, but not because we are so special,  but because there were only four people in the theater, and Sarah and I were two of the four. Seeing the Jonas bothers sing is not exactly on my list of things to see before I die, but seeing Sarah smile and laugh as often as possible is. It was the best feeling ever to see Sarah singing and dancing a memory that I will never forget as long as I live. Take care everybody and God bless. I know a thanks isn't necessary, but I thinks it's great that you all still keep us in your prayers, and that you still keep up with what Sarah is doing, and more importantly how her health is doing.
 Much Love,
Sarah's Parents,Larry and Margaret

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