Hooray! The day has finally come! After finalizing our new website and video, you can view the first part of our Myocarditis Foundation Video, “How the Myocarditis Foundation was Founded”…
We are proud to announce that on Monday June 20, 2016 the Myocarditis Foundation will be hosting its first gala to raise funds to further research a cure and awareness…
June 10-15, 2016 in Cleveland, Ohio Celebrating the Gift of Life – “All Roads Lead to Cleveland” The Donate Life Transplant Games© is a festival style multi-sport event for participants…
This week I had the pleasure of participating in Rare Disease Week in Washington, D.C., which was organized by the Rare Disease Legislative Advocates (RDLA). It is the 5th year…
On Monday February 29 th, Candace Moose, Co-Founder of the Myocarditis Foundation, attended New Jersey Rare Disease Day. Rare Disease Week is a global event sponsored in the US by…
The Myocarditis Foundation 4th Annual Patient, Family and Researcher Meeting will be held again in conjunction with the Heart Failure Society of America (HFSA) conference on Friday evening September 16th…
Myocarditis, what a tongue-twister of a word. A word that most people never hear until it affects them or someone they know. A word that many who hear it, wish…
What an awesome day in Edina, Minnesota today for the 3rd annual Quinn’s Cup Pond Hockey Tournament, in memory of Quinn Kirsch. Quinn was an 8 year old who died…
To all our California friends and family or if you will be in the Southern California area on Tuesday February 9th…. Candace Moose will be in town to raise awareness…
The year 2016 may have just begun, but Dr. Leslie Cooper is already scheduled to speak at many various conferences around the world on Myocarditis. This one in particular, “The…
