Regional Ambassadors
Connect with Regional Ambassadors via email. We’d love to speak with you and discuss local resources for you and your child with MEF2C Related Syndrome. STAY TUNED for the Regional Rep Resource Guide and our updated Events page to explore opportunities to meet other families and to attend MEF2C-friendly events in your region.
Be inspired by MEF2C advocacy efforts of the Olson family in Minnesota, and MEF2C Awareness Day on May 14th.
Follow the journey of a MEF2C family, and learn more about key early intervention targets.
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Laura Durns
Mid-Atlantic
Pennsylvania
Laura has a son with a MEF2C variant
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Anne Lenzin
Mid-Atlantic
New York
Anne has a son with a MEF2C variant
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Suzanne Bean
New England
Massachusetts
Suzanne has a son with a MEF2C variant
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Judy Daprano
Southeast
Florida & Georgia
Judy has a daughter with a MEF2C variant
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Tom Westermyer
Southeast
Florida
Tom has a granddaughter with a MEF2C variant
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Kelly Olson
Midwest
Minnesota
Kelly has a daughter with a MEF2C variant
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Stella Jeong
Midwest
Illinois
Stella is a DPT on our Therapeutic Advisory Board and has a daughter with a MEF2C variant
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Jennifer Bhalia
Pacific Northwest
Oregon
Jennifer has a son with a MEF2C variant
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Amanda Pedrajas Gual
President & Founder
Amanda is the president and founder of the first MEF2C advocacy organization world-wide
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Marija Max
International Representative
Germany
Marija is leading MEF2C advocacy in Germany
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Josephine Schembri
International Representative
Malta / Italy
Josephine is leading MEF2C advocacy in Malta

