Rare Disease Report: Myocarditis Foundation Origins and Current Focus

Candace Moose, Co-Founder and President of the Board of the Myocarditis Foundation, was interviewed by the Rare Disease Report about the origins of the Myocarditis Foundation and what the Foundation’s current focus.

The link below contains the video interview with Rare Disease Report interview with Candace Moose

Rare Disease Report: Myocarditis Foundation Origins and Current Focus