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

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Posted byewefoundationSeptember 10, 2020May 12, 2021Posted inElijah

It’s all about that orange and blue, baby! Y’all ain’t ready!

Posted byewefoundationSeptember 10, 2020May 12, 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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