Meet the Team

Parent Project Muscular Dystrophy’s staff is a dedicated group of passionate people that continually work to assist families in the community. They are available to help round the clock and are deeply committed to fight to end Duchenne.

Find contact information for PPMD’s team members below, or contact us by phone at 800-714-5437.

Pat Furlong

President & CEO

Ryan Fischer

Chief Advocacy Officer

Kaylan Moitoso

Chief Business Officer

Niki Armstrong, MS, CGC

Director, Community Research & Genetic Services

Eric Camino, PhD

Vice President, Research & Clinical Innovation

Brian Denger

Community Engagement Coordinator

Erin Dresnick

Director, Development

Megan Freed

Data and Technology Strategist

Jody Gabbard

Executive Assistant

Kimberly Galberaith

Creative Director

Nicole Herring

Vice President, Development & Community Engagement

Maria Iacullo

Finance Administrator

Stephanie Ivanov

Director, Online Communication, Strategy & Engagement

Kathi Kinnett, MSN, CNP

Advisor, Clinical Care

Ann Martin, MS, CGC

Vice President, Community Research & Genetic Services

Patrick Moeschen

Coordinator, Adult Advocacy & Engagement

Rachel Schrader, MS, APRN, CPNP-PC

Vice President, Clinical Care & Education

Dr. Mena Scavina, DO

Advisor, Certified Duchenne Care Center Program

Ellen Wagner

Coordinator, Clinical Care & Education

Amanda Wilkison, RN, BSN

Director, Clinical Care & Education