Awareness of Polymyositis

Home Awareness of Polymyositis

MSU Turns 2 years-old!! Our wish, Celebrate your Caregiver. And, share what you did to celebrate!

Author:

Myositis Support and Understanding Association (MSU) is a 501(c)(3) nonprofit organization with a mission to improve the day-to-day lives of Myositis patients. MSU is a patient-centered organization, founded by Myositis patients, for Myositis patients, and believes education, support, advocacy, and assistance are key to helping patients and caregivers. As a nonprofit, we rely on donations for funding and volunteers to help manage our fast growing organization.

View more information: Myositis Support

Related Articles

Upcoming Events

  • ILD and Myositis Video Chat with Fiona September 21, 2017 12:00 pm - 1:30 pm
    ILD and Myositis Video Chat, September 21, 2017

    Register today: Fiona, living with Dermatomyositis for three years and ILD for two years, has realized the importance of being proactive about her lung issues. Some of the things she does are based on research, others are based on her personal experience. She is not a doctor but is delighted to share how she deals with it on an everyday basis. Join in this video chat session to hear Fiona’s experiences, ask questions, and share what works for you! Fiona led a video chat, “Myositis and Food with Fiona” that was excellent! You don’t want to miss this one.

© Myositis Support and Understanding Association, Inc. 2010-2017. All Rights Reserved. MSU is a 501(c)(3) nonprofit organization.

You agree to our Terms and Conditions and Privacy Policy by using and viewing our site.

Want to make a tax-deductible donation? Visit our Donate page today!

PIONEER, Idera clinical trial for dermatomyositis

PIONEER, Idera clinical trial for dermatomyositis

 Log in with Facebook
or

Log in with your credentials

or    

Forgot your details?

 Log in with Facebook
or

Become a Member

Send this to a friend