Dr. Leslie Cooper attended the 11th Myocardial and Pericardial Disease Working Group, part of the European Society of Cardiology, this past week in Tel Aviv, Israel. The Myocarditis Foundation was…
Rare Disease Week on Capitol Hill will take place in Washington, D.C.,from February 23-27. The five day event includes a rare disease documentary film screening , an art show , a…
The incidence of myocarditis in children is uncertain but it is estimated that 1 per 100,000 children per year are affected. It has been reported that 0.05% of all pediatric…
The parents and siblings of Quinn Kirsch honored his memory again this year with an annual hockey tournament. 400 kids, many of them his friends, turned out in Edina, Minnesota,…
The Myocarditis Foundation Board of Directors Meeting and Training was an exciting time as we are celebrating our Tenth Anniversary since IRS approval as a nonprofit. Candace Moose opened the…
The Myocarditis Foundation is pleased to announce that it will be funding a research fellowship grant for the 2015/16 grant cycle. The Myocarditis Foundation will be funding a research grant…
January 5th, 2015 Dear Myocarditis Foundation Friends & Families, I am writing to tell you that I have resigned as Director of the Myocarditis Foundation. Following the birth of my…
Candace Moose, Giant Cell Myocarditis survivor due to a heart transplant and co-founder of the Myocarditis Foundation, wrote a beautiful and eloquent book tracking her experience of her heart transplant.…
Written by: Hamish Deery October 11, 2014: Kona, Hawaii The alarm went off at 4:15 am but I was already awake. The rest of the family was bleary eyed but…
The Myocarditis Foundation is announcing the launch of their Tribute Cards! Tribute Cards are given for any reason that one might purchase a greeting card; however, it includes the acknowledgement…
