A Light in the Dark: My Realities with Dermatomyositis
How can I raise awareness if I'm not honest and real about all that comes with dermatomyositis?
How can I raise awareness if I'm not honest and real about all that comes with dermatomyositis?
My mystery disease actually shows up as a result of the loves of my life. A mystery that is so worth each 9 months. No...
Stand Strong Together, Myositis Warriors!
Living the #MyositisLIFE for many of us.
I’m overwhelmed. I’m scared. I’m tired. I’m tired of new symptoms, new scares, new tests. But I am not alone!
Myositis Empower Walk Newsletter (MEWN) Edition Two. The Landman's speak with last year's Myositis Empower Walk top team fundraising captains about how team fundraising can...
Welcome to May 2021, Myositis Awareness Month. Join Myositis Support and Understanding in fundraising, educating, and supporting!
Purchase Myositis Awareness Apparel in this limited time, 3 design series available in hoodies, Raglans, and t-shirts. Proceeds support us at MSU.
Our dad's time with dermatomyositis was only a small portion of his life, although a very monumental time in our life.
Part 2 includes information to help guide local physical and occupational therapy teams and various exercise demonstrations for myositis patients and how to modify them.
We need plasma donors or we face a shortage of life-saving immunoglobulin therapy used to treat myositis and many other diseases. Join the #ItsMyTurn campaign.
Paul shares five important elements at the Heart of Caregiving from his own personal story as a Parkinson’s caregiver.
I wear a mask because I have no spleen and I am on medication for necrotizing autoimmune myopathy.