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

Raymond Belanger Deloge

Translational Genomic Medicine Specialist & Community Outreach Coordinator

Dr. Maya Chopra (MBBS, FRACP)

Acknowledgments

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

Special thanks to our parent/patient 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.