Myositis Support and Understanding (MSU) is once again a Top-Rated Award from GreatNonprofits! It is through you sharing your experiences about our organization that we get this great honor.

Read inspiring stories about how we are empowering myositis patients and caregivers and add your own!

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At Myositis Support and Understanding (MSU), we believe in transparency. We have been a Platnum organization since 2017.

You can learn more about our organization, our goals, financials, and more by visiting us on Guidestar.

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MSU is a Member of the Community Congress

Myositis Support and Understanding (MSU) is working at the national level, through EveryLife Foundation’s Rare Disease Community Congress Working Groups, in addition to working on the COVID-19 ad hoc committee, the MSU Board is lending our input in three critical areas:

(1) public policy,

(2) access to approved therapies,

(3) improving the regulatory process and advancing regulatory science for rare disease therapies.

We support the STAT Act! Talk to your legislators today.

Myositis Support and Understanding Association, spotlight Accessibility.com

Myositis Support and Understanding (MSU) was one of the initial organization spotlight nonprofits. We are proud to be listed and associated with Accessibility.com. Be sure to check it out.

Myositis Support and Understanding is a proud Global Genes Rare Foundation Alliance Member

© 2021 Myositis Support and Understanding Association (MSU). All rights reserved. | View our Privacy Policy, Terms, and Non-Discrimination policy. MSU is a charitable organization with 501(c)(3) tax-exempt status. Federal ID #47-4570748.

View COVID-19 resources and updates, and stay tuned to your state, local, and federal health agencies, along with the CDC.

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