A Global Advocacy Network for Families with Rare Diseases and the Professionals Who Serve Them

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Me and Dad

Posted byewefoundationJanuary 22, 2021February 24, 2021Posted inElijah

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Posted byewefoundationJanuary 22, 2021February 24, 2021Posted inElijah

Published by ewefoundation

The E.WE Foundation is a global healthcare advocacy organization providing resources and support to families impacted Trisomy 18 (Edwards Syndrome) and other rare diseases. View more posts

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_{The information provided by the E.WE Foundation is for educational and informational purposes only and is not intended to replace the advice of a physician or other qualified medical or social service professional.}

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