Regional Representatives

Connect with regional representatives 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.

Follow the journey of a MEF2C family, and learn more about key early intervention targets.

  • Tushar Puthran

    Mid-Atlantic

    New Jersey

    Tushar has a daughter with a MEF2C mutation, born in 2017

  • Anne Lenzin

    Mid-Atlantic

    New York

    Anne has a son with a MEF2C mutation, born in 2013

  • Kelly Olson

    Midwest

    Minnesota

    Kelly has a daughter with a MEF2C mutation, born in 2021

  • Michelle Busch

    Midwest

    Ohio

    Michelle has a daughter with a MEF2C mutation, born in 2008

  • Rachel Pignotti

    Midwest

    Illinois

    Rachel has a son with a MEF2C mutation

  • Ann Mathews

    Southwest

    Texas

    Ann has a daughter with a MEF2C mutation, born in 2020

  • Judy Daprano

    Southeast

    Florida & Georgia

    Judy has a daughter with a MEF2C mutation, born in 2003

  • Amanda Pedrajas Gual

    Amanda Pedrajas Gual

    President & Founder

    MEF2C Association Spain

    Amanda is the president and founder of the first MEF2C advocacy organization world-wide

  • Marija Max

    International Representative

    Germany

    Marija is leading MEF2C advocacy in Germany

  • Josephine Schembri

    International Representative

    Malta / Italy

    Josephine is leading MEF2C advocacy in Malta