Blog - Page 19 of 20 - The Myositis Association

Stanley Prather: Dermatomyositis

February 3, 2018June 14, 2018

Stanley was diagnosed with dermatomyositis in 2008 after 18 years of symptoms. Before his diagnosis, Stanley visited multiple heart and liver doctors who were convinced his symptoms were due to other medical issues.

Carolyn Ester: Sporadic Inclusion-Body Myositis

November 26, 2014June 14, 2018

Carolyn is a nurse from Wichita, Kansas. She was diagnosed with sporadic inclusion-body myositis in 2010 after three years of symptoms and three doctors.

John Mozer: Sporadic Inclusion-Body Myositis

January 29, 2013June 14, 2018

John Mozer is a retired consulting structural engineer and amateur astronomer from Aurora, Colorado. John was diagnosed with sporadic inclusion-body myositis in 2006.

Dale Scott: Polymyositis

January 26, 2013August 20, 2018

Dale is a member of The Myositis Association and sits on our Board of Directors. Before being diagnosed with polymyositis, she worked through several doctors and dealt with a variety of complications.

Bill Simeral: Polymyositis

November 26, 2014June 14, 2018

Bill Simeral is from Wheaton, Illinois, a suburb of Chicago. He was diagnosed with lupus and polymyositis in 2005, followed by autoimmune hepatitis and other complications. He has since learned how to cope with his diagnosis.