A touching personal story from the daugher of a myositis patient remembering that her Dad, her longtime hero, ...
MSU is a 501(c)(3) non-profit organization founded on July 30, 2015, for patients living with, and for loved ones...
Helping family members understand the merry-go-round of chronic illness from a spouse’s perspective
, , Caregiver
A recurring topic of conversation in health support groups is the difficulty spouses, partners, parents, siblings, children, or friends...
Myositis Support and Understanding recently spoke with Rich and Carla Stevenson, David Quay, and Barry Pace about life with...
12 things your chronically ill friend wants you to know about feeling left behind, and what you can do to help!
, , Myositis, Myositis Life Hacks
One of the worst things someone with chronic illness can do is make a mistake in the balance between...
Myositis Awareness Day And My Husband’s Diagnosis by Guest Author, Barbara Naturally Speaking It’s been almost three years since...
Hi, I’m Sage and I am nine years old. My mommy has dermatomyositis. I have a list about the...
Today Jerry Williams, founder and president of MSU, is interviewing our very own, Emily Filmore. She is an MSU...
The week after all the double lung transplant evaluation testing is a long one. Our hospital meets on Tuesdays,...
Myositis Support and Understanding supports Caregivers and offers several online support groups for Caregivers, Family and Friends. We also...
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