Maureen Hume shares her experiences living with Inclusion Body Myositis, staring years before her diagnosis.
This is a collection of personal, user submitted stories.
We learn from the experiences of others, so we want Myositis patients, caregivers, family members, and friends to share their stories of what life is like living with the rare disease, Myositis, and its subtypes.
Some would say that this should have been the worse moment of my life, however, it has proven to...
September 21 @ 2:00 pm - 3:30 pm EDT
September 27 @ 5:00 pm - 6:30 pm EDT