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The E.WE Foundation

Non-profit Organization Management

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The E.WE Foundation
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    Sarita Edwards CEO | Global Speaker | Podcaster | Award Winning Advocate | Social Health | Digital Creator | Trisomy 18 | Rare Diseases | Expert | JEDI | Public Policy
    • Huntsville, Alabama, United States
    • Rising Star
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    Kelly Plunkett Director of Programs I TEA Enterprise Support I Agilest
    • Denver, Colorado, United States
    • Rising Star
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    Sarita Edwards Rare Mom | MHA | Certified Mental Health First Aid Instructor | Global Speaker | Keynote | Podcaster | Award Winning Advocate | Social Health | Digital Creator | Trisomy 18 | Rare Diseases | DEI | Public Policy
    • Huntsville, Alabama, United States
    • Rising Star
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    Kareem Edwards BSc(Psych),VP Operations | Parent Advocate | RARE Parent | Trisomy 18 | RARE Disease
    • Madison, Alabama, United States
    • Rising Star
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Overview

The E.WE Foundation is an IRS approved 501(c)(3) nonprofit healthcare advocacy organization. MISSION To support families affected by Edwards Syndrome or Trisomy 18 and other rare diseases, while changing the medical perspective through advocacy, education, and public policy. VISION To ensure all families affected by Edwards Syndrome, Trisomy 18 and other rare diseases, have equitable access to quality healthcare, early intervention, and social services VALUES We believe patients with chronic illness like Edwards Syndrome, Trisomy 18 should have immediate access to quality healthcare, medical resources, and economic support, without bias or prejudice.