Open Enrollment for the insurance marketplace for coverage starting 2018 begins on November 1st and ends December 15, 2017....
Myositis News and Updates
MSU is a 501(c)(3) non-profit organization founded on July 30, 2015, for patients living with, and for loved ones...
A wife, sister, soldier, student, and a daughter. Life was great. 22 years old and nothing seemed impossible. The...
Chronic Illness, Myositis, and Depression: The following are the comments I gave to a support group about my book,...
I truly have a passion and desire to prevent others from going through what I've gone through! I...
May is Myositis Awareness Month. Myositis Support and Understanding commemorates the month with patient-centered events. Our theme, "With Myositis,...
Learn more about Rose's experience on Capitol Hill during Rare Disease Week 2017. Find helpful links to Advocacy organizations...
As you probably know, we have lost many of our MSU group members throughout the past couple of years,...
Although everyday life seems like a mad dash to the finish line honestly it’s all about staying the course...
Investigators are seeking people with dermatomyositis to participate in a phase 2 clinical trial of the experimental drug IMO-8400....
11 Ways to Be Intimate When You Have Chronic Illness and Sex Is Difficult
February is the month of love. Chocolate-covered strawberries, roses, sensual massage oils, lingerie, and champagne — we see reminders...
Prednisone Withdrawal: As a patient with #myositis, you are likely on, or have been on, prednisone at some point....
Sadly, my mum lost her battle as an IBM warrior
Mums journey was a very difficult one. I remember her first fall the day I gave birth to...
We hope that your involvement with Myositis Support and Understanding (MSU) has allowed you to feel more included and...
A short story about Jerry Williams, president of MSU, and getting involved
It has been over 13 years since Jerry Williams, president of MSU, was diagnosed with Polymyositis, sometimes simply referred...
I think we often neglect to hear what our children and younger family members think about us living with...
Myositis Support and Understanding is hosting a fundraiser and requesting volunteers for #GivingTuesday, a global giving movement that has...
As we continue our rapid growth, we are looking for volunteers and Board Members who are interested in donating...
When visiting a new doctor, patients are usually supplied with a number of information packets that are to be...
Learn more about Lynn Lizarraga and her online video laughter yoga program she provides to members of Myositis Support...
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