Mission
The Myasthenia Gravis Foundation of America (MGFA) is dedicated to improving the lives of individuals affected by myasthenia gravis, a chronic autoimmune neuromuscular disorder characterized by fluctuating muscle weakness. Founded in 1952, the MGFA aims for a world without MG by advocating for patient support, funding research for better treatments, and providing education and resources for patients, caregivers, and healthcare professionals.
Basic Information
Founded in
1952
EIN
13-5672224
Total Assets
$11.36 million
UN Sustainable Development Goals Supported
This organization contributes to the following United Nations Sustainable Development Goals. See the SDG page for more information.
At a Glance
MyMG Mobile App
An app designed to help patients manage their myasthenia gravis.
MGFA Helpline
A support line available to assist individuals affected by MG.
MG Walk Fundraising Events
Annual fundraising events that unite the community to raise awareness and support for MG.
Impact Stats
Registry Participants
MGFA Global MG Patient Registry
Started a comprehensive registry to collect and analyze data on patients with myasthenia gravis.
Social Media Followers
Increased Awareness
Significantly raised awareness about myasthenia gravis through various campaigns.
Research Grants
Funded Research Grants
Provided funding for groundbreaking research aimed at understanding and treating myasthenia gravis.
Past Events
2023 Annual Conference
2023-06-12
Annual MGAA Conference bringing together patients, families, and medical professionals.
MG Community Health Fair
2023-08-15
Community health fair providing resources and information about myasthenia gravis.
Upcoming Events
MGFA Community Health Fair - Tampa Bay Area
2024-11-02
A community health fair connecting patients with resources and support.
Learn More
2025 MGFA National Patient Conference
2025-03-23
An annual gathering for patients and their families to learn and share experiences.
Learn MoreOur Programs
Myasthenia Friends Program
A peer support program connecting individuals with similar experiences.
Learn MoreVolunteer Opportunities
Impact Reports
MIP Score (Beta)
The MIP Score is in beta! We'd love any feedback you may have.
The MIP Score and it's methodology is purely used as a way to visualize how a nonprofits public financial data compares against others. It doesn't reflect the unique circumstances and impact that a nonprofit has.The MIP Score should never be used to say one charity is better than another.
Overall Score
75
84
/100
Program Expense Ratio
74.63%
10
/20
Program Revenue Growth
138.59%
20
/20
Leverage Ratio
0.1171
18
/20
Working Capital Ratio
2.647
16
/20
Fundraising Efficiency
0.1218
20
/20
Latest Filing Data: Form 990
Fiscal Year:2022
Source:Source: Self-reported by organization
Financial Details
Revenue
| Category | Amount | Percentage |
|---|---|---|
| Contributions, Gifts, and Grants | 3.609M | 82.23% |
| Program Services | 452.1K | 10.30% |
| Investment Income | 252.4K | 5.75% |
| Sales of Non-Inventory Assets | 22.84K | 0.52% |
| Other Notable Sources | 3.946K | 0.09% |
| Total Revenue | 4.389M | 100.00% |
Related Nonprofits
South Carolina Advocates for Epilepsy
Med Research
Epilepsy ResearchCervical Spine Research Society Inc.
Med Research
Epilepsy ResearchKhristin Kyllo Memorial Fund
Med Research
Epilepsy ResearchEpilepsy Institute of North Carolina
Med Research
Epilepsy ResearchLove for Liam Foundation
Med Research
Epilepsy Research