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.
Chopra-Amiel-Gordon Syndrome (CAGS) Foundation, Inc.
Dedicated to finding CAGS treatments and a cure.
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