Myositis-Induced Depression
Author: Emily Filmore
Emily A. Filmore is an author, speaker, and is one of the founding board members of Myositis Support and Understanding Association. She wrote "The Marvelous Transformation: Living Well with Autoimmune Disease" about her experiences with dermatomyositis and other chronic illness (Central Recovery Press 2015), the "With My Child" series of children's books about family bonding (Withmychildseries.com), is the co-author of "Conversations with God for Parents" with Neale Donald Walsch and Laurie Lankins Farley. (Rainbow Ridge, 2015), and co-author of “Parenting through Divinity” with Laurie Lankins Farley (due for release in 2018 through the Waterside imprint).
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[…] Myositis and depression were not only affecting me, but they were also affecting my parents, my partner, my family members, and friends. The fact that most of my friends stopped coming around or even calling made it even worse for me emotionally. I needed and wanted, that companionship and laughter. I also had extreme feelings of guilt about people taking care of me. They were giving up their time and energy to help me and it was unthinkable in my mind, even though I would have done the same in their position. And, I felt that no matter how much I explained it, no one would ever truly understand what my life was like living with myositis because on the outside I didn’t really look sick. This is a part of a battle living with invisible illnesses. […]
[…] Myositis and depression were not only affecting me, they were affecting my parents, my partner, my family members, and friends. The fact that most of my friends stopped coming around or even calling made it even worse for me emotionally. I needed and wanted, that companionship and laughter. I also had extreme feelings of guilt about people taking care of me. They were giving up their time and energy to help me and it was unthinkable in my mind, even though I would have done the same in their position. And, I felt that no matter how much I explained it, no one would ever truly understand what my life was like living with myositis because on the outside I didn’t really look sick. This is a part of a battle living with invisible illnesses. […]