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Miracle Child Megan - Penn State Hershey Children's Miracle Network

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Uploaded by on Jun 9, 2010

http://pennstatehershey.org/cmn Megan's lifelong struggle with Ehlers-Danlos syndrome and her care and treatment at Penn State Hershey

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  • I continue to be inspired by Meg and Jeremy each day and hope someday k,EDS will be better known and pray they will always have access to the care they need to live the healthiest lives possible.

  • My son Jeremy is 7 and has type VI EDS also. I talked to you briefly several months ago, but Megan wasnt doing so well at the time. Glad to see she is doing better. This is a very inspiring video. Joe Thurman.

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