There is no slider selected or the slider was deleted.
Author: Jerry Williams
Jerry Williams, the Founder and President of MSU, was diagnosed with Polymyositis in 2003 at the age of 27. Since his diagnosis, Jerry has made it his mission to help others living with the rare disease, Myositis. To this effort, Jerry is involved in many different aspects such as education, writing, helping support and answer questions from patients and caregivers, social networking and website development, and much more. (NOTE: Some things are posted under Jerry Williams but he is not the true author. This is because he manages the website.)
View more information: Jerry Williams
Search our site
December 20, 2017 4:00 pm - 5:30 pm
Myositis patients, mark your calendar and join us for this free video support session with Sarah Harrington on Dec. 20th, 4PM Eastern Time. This session is tailored to those diagnosed with, or suspected of having, Polymyositis, Dermatomyositis, Necrotizing Autoimmune Myopathy, Juvenile Myositis, and other unspecified or nonspecific idiopathic inflammatory myopathies (myositis). We have a separate dedicated session for IBM patients as their needs tend to be different.
December 29, 2017 4:00 pm - 5:30 pm
IBM patients, mark your calendar and join us for this free video support session with Mary Jane on Dec. 29th, 4PM Eastern Time. Share experiences, ask questions, compare notes, and make new friends. This session is tailored to those diagnosed with, or suspected of having, Inclusion Body Myositis.