Marilyn McGrath shares her Myositis Life for Myositis Awareness Month and MSU’s #MyositisLIFE project. 

My life changed dramatically in 2006 when symptoms of Dermatomyositis started. I am not able to do all the things I did before, but I have learned to live with Myositis by adapting my lifestyle. I miss taking care of my grandbabies the most, but my life still revolves around my family, they are my everything.

Author: Marilyn McGrath

 


 

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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.

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