DCMFoundation

The newly redesigned DCMF website helps patients & families navigate post-diagnosis with confidence—from understanding genetics and gene testing to finding support groups, educational webinars, and specialists. No one should have to figure this out alone.

dcmfoundation.org

Attention BAG3 patients! On November 16, join Dr. Neal Lakdawala & Dr. Jonathan Lu for a patient-friendly discussion of BAG3-associated DCM, clinical research, and ways to find support.

Register for free: dcmfoundation.org/upcoming-webin…

NEW Study Location: NYU Langone Health
Learn more about this study at: geneticcardiomyopathy.org/UPBEAT

💚 As we share this video again, we invite you to learn about the Genetic Cardiomyopathy Registry—a way for eligible participants to contribute to research. Explore the registry, find answers to common questions, and learn how to participate:
geneticcardiomyopathy.org/genetic-cardio…

Last week we provided an update on our gene-specific support groups. There is a similar group for Gene-Elusive patients, which is a patient's genetic testing did not identify a disease-causing genetic variant that explains their cardiomyopathy.

Join now: dcmfoundation.org/gene-elusive-d…