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Sarah: Appreciate Every Day for #MyositisLIFE

Home Sarah: Appreciate Every Day for #MyositisLIFE

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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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Myositis patients and caregivers can connect with others who understand what they are going through by joining our support community via the Inspire iOS app or by visiting our Myositis Support Community.

Upcoming Events

Myositis Patient Video Support, third Saturdays session at 3 PM ET
Sat 17

Monthly Saturday Afternoon Myositis Patient Video Support

April 17 @ 3:00 pm - 4:30 pm EDT
IMNM Patient Video Support, last Saturday of the month at 3 PM ET
Sat 24

Monthly Necrotizing Myopathy Patient Video Support session

April 24 @ 3:00 pm - 4:30 pm EDT
DM, PM, and ASyS Myositis Patient Video Support
Wed 28

DM, PM and Antisynthetase Syndrome Patient Video Support

April 28 @ 7:00 pm - 8:30 pm EDT

View More…

© 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.

The best way to prevent catching or spreading coronavirus is thorough hand washing, social distancing, and social isolation. Should you begin experiencing symptoms of coronavirus, which include fever, cough, and shortness of breath, please contact your doctor immediately. 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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