Living with DCM Archives - DCM Foundation

Jim’s DCM Story – “The Hardcore Battle.”

Posted on August 3, 2023

“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

DCM Basics – Causes, Symptoms and Treatments

Posted on July 20, 2023

Please click on this link or the image above to view a recording of this webinar and learn about: Causes of DCM Symptoms of DCM and How is DCM Diagnosed Stages of Heart Failure Common Treatments for DCM Q&A Session with a Cardiologist Additional Resources & Information: Treatments for DCM: https://dcmfoundation.org/living-with-dcm/treatments-for-dcm All DCMF Recorded Webinars: https://dcmfoundation.org/webinars-news/recorded-webinars Genetics and

Meet Our New Director of Patient and Family Services – Adam Burkhart

Posted on June 5, 2023

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

Heart Failure Awareness Campaign 2023 – Highlight Heart Failure and Save Lives

Posted on May 1, 2023

New initiative by Global Heart Hub aims to raise public awareness of heart disease More than 60 million people worldwide are affected by heart failure. A MAJOR global initiative during the month of May aims to raise public awareness of Heart Failure in an effort to save lives. The Global Heart Failure Awareness Month 2023

“Healthy Together” Wellness Program – Webinar & Next Program Dates

Posted on April 17, 2023

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

One Family’s Story of Genetic Cardiomyopathy – Awareness is Key

Posted on March 28, 2023

Lea Geli’s story is one that spans three generations and it epitomizes how important it is for doctors and patients alike to be aware of the genetic risks of cardiomyopathy. Lea knew heart failure caused her father’s passing, but didn’t know the details. He was relatively private in his own life and didn’t share many

New & Improved DCMF Website Navigation – Easier to Find What You Need

Posted on January 30, 2023

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

Support for Your DCM Journey – DCMF Programs, Services, and Helpful Advice

Posted on January 20, 2023

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.

Pneumonia Vaccination Guidelines for Cardiomyopathy Patients

Posted on November 28, 2022

Adults 19 through 64 Years Old The CDC recommends pneumococcal vaccination for adults 19 through 64 years old who have certain chronic medical conditions or other risk factors, including: Chronic heart disease, congestive heart failure, and cardiomyopathies Ask your doctor if getting a pneumonia vaccine is right for you. To read the full CDC guidelines

Living with DCM