MSU has given $250k in Myositis Patient Financial Assistance!

In just 5 years, we have given a quarter of a million dollars ($250,000) in Myositis patient financial assistance!

Financial Assistance programs are rare, even in the rare disease space. We understand living with a rare disease like Myositis is expensive and the need for financial assistance is real. Since 2017, we have helped hundreds of people with Myositis in these categories: mobility/assistive equipment, medical bills – not a copay assistance program – and emergency household expenses.

And this year we increased the maximum award from $1,500 to $2,000. It’s only through your generosity as fellow patients, donors, sponsors, supporters, and MSU volunteers that this was even a possibility. And now, in 2022 alone, we will provide $100,000 in assistance!

See the Myositis Support and Understanding Financial Assistance infographic below. Click on the image to view the PDF version.

MSU Financial Assistance Infographic

Click image to view the full PDF

Would you like to contribute?

Make a one-time or recurring donation to our program. It’s only when we come together and give what we are able to that we can continue to improve the quality of life for those living with Myositis.

MSU Myositis Patient Financial Assistance Program

If you are living with Myositis, learn more about the program and download the application and help guide.

Learn more about our Financial Assistance Program.

 

 

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Myositis Support and Understanding Association (MSU) is a patient-centered, all-volunteer 501(c)(3) nonprofit organization Empowering the Myositis Community. Founded by Myositis patients, for Myositis patients, MSU provides education, support, advocacy, access to research and clinical trial matching, and need-based financial assistance.

View more information: Myositis Support

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