Join starting at 8PM Eastern for Video Support session for caregivers and care partners of those diagnosed with idiopathic...
Video Support session for caregivers and care partners of those diagnosed with Polymyositis, Dermatomyositis, Inclusion Body Myositis, Necrotizing Autoimmune...
Register and join MSU and Lynn L. for an interactive "Exercise Through Laughter" online session, March 20th, 7PM Eastern....
Introducing the NEW Myositis Support Community! The Myositis Support Community is similar to Facebook, however, it provides a more...
Join us for our free Myositis Laughter Yoga Video Activity Session with Laughter Yoga Instructor Lynn Lizarraga. Laughter is...
Join us for our free Myositis Laughter Yoga Video Activity Session with Laughter Yoga Instructor Lynn Lizarraga. Laughter is...
Join us on Tuesday, August 14th starting at 2PM Eastern for our free Myositis Laughter Yoga Video Activity Session...
Join us for our free Myositis Laughter Yoga Video Activity Session with Laughter Yoga Instructor Lynn Lizarraga. Laughter is...
Patrick Merel of Portable Genomics will join us on Thursday, June 28, 2018, at 7 PM EDT to discuss...
Myositis patients have special needs when preparing for natural disasters. Learn more and be prepared with a plan
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!
, , Hacks, Myositis
One of the worst things someone with chronic illness can do is make a mistake in the balance between...
5 Week Road trip to Yellowstone with IBM Adventurers by guest author Camille Lesoine Ray and I are back...
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...
Still Alive and Waiting for the Call Parts Five and Six of a series submitted by Anne Tiller While...
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Upcoming Events
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Myositis Caregiver Video Support Session, March
March 26 @ 8:00 pm - 9:30 pm EDT
