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The E.WE Foundation

A Global Advocacy Network for Families and Professionals Impacted by Rare Diseases

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They Thought I Was Sleep

Posted byewefoundationSeptember 24, 2021September 24, 2021Posted inUncategorized

Nope!

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Posted byewefoundationSeptember 24, 2021September 24, 2021Posted inUncategorized

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 E.WE Foundation | PO Box 6391, Huntsville, AL 35813 | IRS approved 501(c)(3) | EIN 84-2765554 | Copyright ©2019-2025. All Rights Reserved.

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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