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
Kaylan Moitoso
Chief Business Officer
Katherine Anderson, ScM, CGC
Community Research Manager, Data Initiatives & Advocacy
Kayla Banks, MS, CGC
Manager, Community Research and Genetic Services
Emily Bent
Director, Communications
Lauren Bogue, MS, CGC
Curator, The Duchenne Registry
Eric Camino, PhD
Vice President, Research & Clinical Innovation
Jennifer Capobianco
Grants Management Coordinator
Hannah Chertock
Communications Manager
Ally Cripe
Development Coordinator
Brian Denger
Community Engagement Coordinator
Megan Freed, MPH
Director, Data and Technology Strategy
Jody Gabbard
Senior Administrative Coordinator
Kimberly Galberaith
Creative Director
Alexis Hazlett, RN, MSN, CPN
Senior Director, Clinical Care & Education
Nicole Herring
Vice President, Development & Community Engagement
Katie Jesionek, BSN, RN
Manager, Clinical Care & Education
Natalie LaRocca
Development Manager
Ann Martin, MS, CGC
Vice President, Community Research & Genetic Services
Kerri McLaughlin
Finance Manager
Rachel Schrader, MS, APRN, CPNP-PC
Vice President, Clinical Care & Education
Lauren Stanford
Senior Director, Advocacy
Ellen Wagner
Community Centricity Manager
Erica Goude, MS, CCRP
Advisor, Certified Duchenne Care Center Program
Patrick Moeschen
Advisor, PPMD Adult Advisory Committee
Mena Scavina, DO
Advisor, Care Programming
