Please click on this link or the image above to view a recording of this webinar and learn about: DCM Basics Overview The Future of DCM Therapies Support for Your DCM Journey Living with DCM – Panel Discussion with 3 Patients Live Q&A
We hope you can JOIN US for our second annual DCM Patient & Family Conference, taking place online Wednesday, October 18th from 6:00-7:30 PM ET. Click HERE to register. This year’s conference features information to help guide you on your DCM journey and three special guest speakers – all DCM patients who are living well
“My story is the hardcore battle.” Jim Hogan has been fighting that battle since he was diagnosed with non-ischemic DCM in December 2021. The six months after his diagnosis were hard because he thought he only had a year to live. He got his affairs in order and started to disappear: he lost weight, sold
We are thrilled to announce that Adam Burkhart has joined the DCM Foundation as Director of Patient and Family Services. In this full-time position, Adam will support DCM patients by creating, implementing, and running the Foundation’s patient and family services and programs. Adam has a wide background of experience. He worked as a plumber/pipefitter for
We’re excited to have Julie Wilde from Transform with Wellness as the guest speaker at this month’s webinar: “DCM Foundation’s Healthy Together Wellness Program.” During this April 19th live event, Julie will share practical tips and ideas for healthy living – from diet and exercise to mindfulness, sleep and stress management. Julie is a certified
The DCM Foundation website has been reorganized to provide you with faster and easier access to the information you need. This website provides the most current information and resources available to DCM patients and their families. The redesigned homepage gives you links to access important information about DCM including Symptoms, Stages, Arrhythmias, Causes, and Genetics
Learn helpful health and emotional wellness advice from a DCM patient and a clinical expert. Then, hear about the expanding patient resources the DCM Foundation is working on to support DCM patients in 2023 and beyond.
We heard you! Many DCM patients and family members have expressed a need for local DCM support groups where they can discuss their shared experiences with dilated cardiomyopathy. As a result of your input, we are excited to announce the DCM Foundation is beginning discussions with a number of DCM hospitals and research centers around