Over the past quarter, we have done a major renovation and modernization of the Myocarditis Foundation Website. The website is functionally easier to navigate, and is now fully capable with…
Medscape Rare Disease Crusader: Leslie Cooper, MD From 1905 to 1993 there were only 90 reported cases of giant cell myocarditis, the cardiac condition Cooper specializes in treating. Today, there…
AWaRDS Study: Adults with Rare Disorders Support What is the study about? In partnership with the National Organization for Rare Disorders, this will be the first large-scale study about the information and psychosocial support needs of people living…
2nd Annual Myocarditis Foundation Gala Awareness Event and Fundraiser: June 22, 2017 The Myocarditis Foundation has aligned the 2017 Family Support Weekend to kick off directly after the Myocarditis Foundation…
The 1st Annual Myocarditis Foundation Gala was held on Monday June 20th at the Mandarin Oriental in New York City. The event was held in honor of Matthew Corso, a…
Texas Children’s Hospital and the Myocarditis Foundation Symposium for Community Healthcare Professionals on: Myocarditis, Cardiomyopathies and Sudden Death in Children (March 25, 2017 8am to 4pm) Dr. Jeffrey Towbin, Keynote…
The Myocarditis Foundation is excited to announce that we have received a grant from the St. Jude Medical Foundation to help fund the Revision of the Myocarditis Foundation Website. In…
Hello to all our followers… There are many times when people ask if there are any events coming up in “my neck of the woods”… This event, is held every…
Patty Edgeman, mother of a Viral Myocarditis victim Clayton Edgeman, wanted to do something to raise awareness for the disease that took her son on May 17, 2016 without warning.…
Hello everyone…We know that your lives are often so busy that you do not know where the day has gone and before you know it it is time to go…
