Megan Foster
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Welcome to Megan's Page. My mom created it for everyone to keep up with Megan and her brave big sister Michelle. Megan is post-transplant, counting down the months & years til she is five years clear.

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  THURSDAY, JULY 03, 2008 10:27 AM, CDT
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We are doing good. Besides, Michelle having a bad case of swimmer's ear without being in a pool. This past Saturday was the Mayfield reunion. We all had a good time. Megan really enjoyed wandering around doing her own thing.

This morning I wanted to post because two years ago today we were in PICU and Dr. Frangoul told us we were at a pivotal point. We needed to give Megan time to heal, but time was of the essence and we needed to wing her off the vent. He actually gave us a % of survival when we asked - 20% chance. What we didn't know was that no other child her age at Vanderbilt had come off the oscillatory vent, successfully.

And now, Megan is doing great. Thanks to wonderful Doctors and nurses and God's guidance, many prayers and lots of support.

Tomorrow is the fourth of July. Hope everyone has a wonderful time! Enjoy being with family and friends and remember our troops who can not. Also, tomorrow at 5 EST on channel 9, the Yellow Rookies will be on the evening news - Dave's Diamond Daring. It will also be available on the website: www.newschannel9.com but I can not find the link. I'll check with Rebecca and let you know this weekend.

Keep little Kennedy in your prayers. She had surgery on her neck and is in a halo. Care Pages: KennedyGarcia. Kennedy had Lukeima and has Down Syndrome. Also, Cody's dad just had back surgery (CarePages: CodyMeyer1). Baby Arelis and Jack are doing better. Don't forget to check in on Oliver. He is nearing his 1st anniversary of his BMT but is in the hospital trying to resolve a TPN issue. He has struggled with this for a long time. Hopefully, theyh can get him off of TPN and straightened out. He is also on carepages.com

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EMAIL AUTHOR
mom_of_michelle_megan@yahoo.com