Our mission

To find treatments and a cure for Chopra-Amiel-Gordon Syndrome while fostering a global CAGS community.

Our vision

A world where individuals affected by Chopra-Amiel-Gordon Syndrome have access to effective treatments and a supportive global network.

Meet the Board

The Chopra-Amiel-Gordon Syndrome (CAGS) Foundation, Inc. was co-founded by dedicated CAGS parents Jennifer Wells and Michael Wells. Their passion and commitment to supporting families, advancing research, and raising awareness drive the foundation's mission.

Jennifer Wells

Co-Founder / board of directors

Mike Wells

co-founder / board of directors

Becky Puhl

board of directors

Scientific & Medical Advisory

Maya Chopra MBBS, FRACP
Attending Physician, Division of Genetics & Genomics
Assistant Professor of Neurology, Harvard Medical School

Acknowledgments

We extend our heartfelt gratitude to our dedicated members, researchers, healthcare professionals, and donors.

Special thanks to our parent champions and volunteers who moderate our Facebook group and share their valuable experiences. Your unwavering support fuels our mission and brings hope to families affected by CAGS.

Contact Information

Chopra-Amiel-Gordon Syndrome (CAGS) Foundation, Inc.
EIN: 33-2923434
1742 S Woodland Blvd. #409
DeLand, FL 32720
Email: info@curecags.org
Registered Agent: registeredagent-dbh@shuffieldlowman.com
Website: https://curecags.org/

Chopra-Amiel-Gordon Syndrome Foundation, Inc. is awaiting approval of our 501(c)(3) tax-exempt status from the IRS. Once approved, this status will be retroactive to our date of incorporation January 15, 2025.