The Parent Project for Muscular logo

The Parent Project for Muscular

WASHINGTON, DC EIN: 31-1405490 Website

Parent Project Muscular Dystrophy (PPMD) is a 501(c)(3) nonprofit organization headquartered in Washington, DC, dedicated to ending Duchenne muscular dystrophy. Founded in 1994, PPMD operates as the largest and most comprehensive nonprofit organization in the United States focused on finding a cure for Duchenne. The organization combines research funding, policy advocacy, care standards development, and community support to address this fatal genetic disorder that affects young men.

Financial Overview

From 2024 IRS Form 990-PF · View filing

Total Assets

$12.6M

+20.4% YoY

Annual Giving

$2.5M

-0.5% YoY

Grant Count

29

+38.1% YoY

Avg Grant Size

$85K

-27.9% YoY

Research compiled by Grantable AI from public sources. Last updated April 2026.

Mission & Focus Areas

Mission: Parent Project Muscular Dystrophy fights to end Duchenne. We accelerate research, raise our voices to impact policy, demand optimal care for every single family, and strive to ensure access to approved therapies.

Primary Focus Areas:

  • Research & Therapy Development: Identifies and funds promising near- and long-term therapeutic strategies for Duchenne and Becker muscular dystrophy. Invests across the development pipeline from basic science to clinical application. Operates the Venture Pathways Program, which invests in early-stage biopharmaceutical companies developing novel treatments.

  • Policy & Advocacy: Raises voices in Washington to impact federal policy and regulatory conversations. Advocacy efforts have secured hundreds of millions of dollars in federal funding for Duchenne research and contributed to eight FDA approvals.

  • Care Standards & Access: Demands optimal care standards and ensures families have access to expert healthcare providers, cutting-edge treatments, and community support. Works to ensure access to approved therapies.

  • Patient Data & Registry: Maintains The Duchenne Registry, established in 2007, which is the largest patient-reported data repository for individuals living with Duchenne and Becker muscular dystrophy and carrier females. The registry strengthens understanding of the disorder and improves care.

  • Community Education & Support: Strengthens, unites, and educates the global Duchenne community through programs and resources.

Grantmaking

PPMD actively funds research and collaborative projects:

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Geographic Focus

Where this funder awards grants

PPMD operates nationally and internationally, with headquarters in Washington, DC. The organization works to strengthen and educate the global Duchenne community.

Grant Distribution by State

27states
+19 more states

Cities

AkronAuroraBaltimoreBerkeleyBerkleyBethesdaBinghamtonBlacksburgBostonBoulderCarmelCharlotteCharlottesvilleChicagoCincinnatiColumbusDallasDetroitEast LansingEvanston

Financial History

Multi-year comparison from IRS filings

2024 Financial Data:

  • Total Revenues: $14,311,761
  • Total Expenses: $12,881,402
  • Total Assets: $12,567,424

2023 Financial Data:

  • Total Revenues: $13.9M
  • Total Expenses: $12.1M
  • Total Assets: $10.4M
  • Total Liabilities: $635k

Staffing: 27 employees

Rating: Four-Star charity with a 100% score based on Accountability & Finance metrics.

Revenue
Expenses
Qualifying Distributions
Net Investment Income
$0$4M$8M$12M$16M201920202021202220232024
Metric202420232022
Total Assets$12,567,424$10,440,900$8,648,654
Revenue$14,311,761$13,881,085$10,753,014
Expenses$12,881,402$12,112,486$11,037,641
Qualifying Distributions
Net Investment Income$150,586$88,569$41,696
Distributable Amount

Giving Over Time

Total grant dollars and number of grants per year

$0$1M$2M$3M$4M57 grants201943 grants202022 grants202123 grants202221 grants202329 grants2024

Grant Insights

How this funder distributes its grants

Top Recipients

Top 10 recipients in 2024

CINCINNATI CHILDREN'S HO…$617KUNIVERSITY OF FLORIDA FO…$300KUNIVERSITY OF ROCHESTER …$210KNYU LANGONE HEALTH$200KUNIVERSITY OF FLORIDA$179KCRITICAL PATH$100KNEW YORK UNIVERSITY$100KOHIO STATE UNIVERSITY$84KNORTHWESTERN UNIVERSITY$74KNATIONWIDE CHILDREN'S HO…$60K

Grant Size Distribution

138 grants across all recorded years

74<$50K27$50–100K21$100–250K12$250–500K4$500K–1M$1–5M$5M+

Open Grants

3 open opportunities from The Parent Project for Muscular

Giving History

Grant recipients and amounts by year

No grants recorded for .

Leadership & Key People

Leadership team and compensation from IRS filings

  • Patricia Furlong — President & Founder
  • Katherine Beaverson — CEO
  • Nicole Herring — Volunteer Coordinator

Compensation Overview

From 2024 IRS filing

PATRICIA A FURLONGPRESIDENT AND CEO$370KKAYLAN MOITOSOCHIEF BUSINESS OFFICER$294KJODI WOLFFCHIEF PROGRAM OFFICER$195KANN MARTINVICE PRESIDENT, COMMUNITY RE…$177KRACHEL SCHRADERVICE PRESIDENT, CLINICAL CAR…$175K

From 2024 filing

NameTitleHoursCompensation
GRETCHEN EGNERBOARD CHAIRMAN8
ALPA KHUSHALANIVICE CHAIR8
DAWN REZKALLATREASURER6
DEANNE FRIARSECRETARY6
DAVID N HOFSTEINEXECUTIVE COMMITTEE6
SUE APKONDIRECTOR2
JEFFREY BIGELOWDIRECTOR2
MARU CHAPURDIRECTOR2
TIMOTHY CRIPEDIRECTOR2
MICHELLE FURLONGDIRECTOR2
LANCE HESTERDIRECTOR2
SUSAN HUANGDIRECTOR2
JOHN KILLIANDIRECTOR2
RICHARD KLEINDIRECTOR2
SCOTT PERRINDIRECTOR2
COLIN RENSCHDIRECTOR2
PATRICIA A FURLONGPRESIDENT AND CEO40$370,075
KAYLAN MOITOSOCHIEF BUSINESS OFFICER40$293,650
JODI WOLFFCHIEF PROGRAM OFFICER40$194,569
ANN MARTINVICE PRESIDENT, COMMUNITY RESEARCH & GENETIC SERV.40$176,600
RACHEL SCHRADERVICE PRESIDENT, CLINICAL CARE & EDUCATION40$174,800

Recent News & Activity

Recent developments and announcements

2025

**Race to End Duchenne Program:** Celebrated its 20th anniversary in January 2025, with 185 team members participating in the Walt Disney World Marathon Weekend in Orlando, Florida.

**Research Collaborations:** PPMD joined collaborative research efforts to decode how human muscle regenerates, expanding its research portfolio beyond direct funding.

Parent Project Muscular Dystrophy Awards $250,000 to Support Clinical Research

**Newborn Screening Initiative:** Awarded funding to support clinical research networks for Duchenne babies identified through newborn screening programs, indicating expansion into early detection and intervention.

Parent Project Muscular Dystrophy Awards $250,000 to Support Clinical Research

Subject Areas

Focus areas based on grantmaking activity

Related Funders

Similar funders by location and focus area

Data last updated April 2026. Sourced from IRS Form 990-PF filings. Research dossier generated April 2026.

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