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

Senior Director, Community Research & Genetic Services

Eric Camino, PhD

Vice President, Research & Clinical Innovation

Jennifer Capobianco

Grants Management Coordinator

Ally Cripe

Development Coordinator

Brian Denger

Community Engagement Coordinator

Erin Dresnick

Director, Development

Megan Freed

Data and Technology Strategist

Jody Gabbard

Executive Assistant

Kimberly Galberaith

Creative Director

Alexis Hazlett, RN, MSN, CPN

Director, Family Support & Case Management

Nicole Herring

Vice President, Development & Community Engagement

Maria Iacullo

Finance Administrator

Stephanie Ivanov

Senior Director, Online Communication, Strategy & Engagement

Jamie Jones

Community Engagement Coordinator

Ann Martin, MS, CGC

Vice President, Community Research & Genetic Services

Patrick Moeschen

Coordinator, Adult Advocacy & Engagement

Kat Piacentino

Communications Specialist

Kayla Quirin, MS, CGC

Community Research Project Manager

Mena Scavina, DO

Advisor, Certified Duchenne Care Center Program

Rachel Schrader, MS, APRN, CPNP-PC

Vice President, Clinical Care & Education

Ellen Wagner

Coordinator, Clinical Care & Education

Amanda Wilkison, RN, BSN

Senior Director, Clinical Care & Education