Company Overview
- Website
- myasthenia.org
- Phone
- (630) 835-0153(800) 541-5454
- Employees
- 37
- Founded in
- 1952
- Industry
- Non-Profit
- NAICS Codes
-
62 - Health Care and Social Assistance621 - Ambulatory Health Care Services6211 - Offices of Physicians62111 - Offices of Physicians621111 - Offices of Physicians (except Mental Health Specialists)81 - Other Services (except Public Administration)813 - Religious, Grantmaking, Civic, Professional, and Similar Organizations8132 - Grantmaking and Giving Services81321 - Grantmaking and Giving Services813212 - Voluntary Health Organizations
- SIC Codes
-
83 - Social Services839 - Social Services, Not Elsewhere Classified
Financials & Stats
Revenue
$5B
Recent News & Media
MGFA International Conference
- Jun 26, 2025
- myasthenia.org
Myasthenia Gravis Foundation of America (MGFA) Kicks Off Myasthenia Gravis Awareness Month Around the World
- May 29, 2025
- prnewswire.com
Myasthenia Gravis Foundation of America (MGFA) Annual MG Patient Conference Features Treatment Progress and Wellness Education
- Mar 31, 2025
- prnewswire.com
What is Myasthenia Gravis?
- Oct 1, 2024
- myasthenia.org
Myasthenia Gravis Foundation of America (MGFA) Announces Global Kickoff of Myasthenia Gravis Awareness Month
- May 31, 2024
- prnewswire.com
Myasthenia Gravis Foundation of America (MGFA) Kicks off Annual National MG Patient Conference With Program Announcements
- Apr 29, 2024
- prnewswire.com
Who is Myasthenia Gravis Foundation of America Inc
The Myasthenia Gravis Foundation of America Inc. is a non-profit organization based in Westborough, Massachusetts. Employing 37 people, the organization generates an annual revenue of $5 million. The organization is dedicated to improving the lives of people living with myasthenia gravis (MG) and finding a cure for this rare neuromuscular disease. MGFA focuses on supporting the MG community through a range of programs, guidance, and education. They also fund research to discover better treatments and ultimately find a cure for MG. Over 70,000 people in the United States alone live with MG, a disease that causes debilitating muscle weakness and fatigue, affecting daily activities such as seeing, swallowing, smiling, walking, and breathing. MGFA strives to be the leading patient advocacy organization for people living with MG. Their mission is to provide comprehensive support while relentlessly pursuing research for better treatments and a cure. For more information about MGFA and their initiatives, you can visit their website at myasthenia.org.
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