About
Founded in 1996, the Hypertrophic Cardiomyopathy Association (HCMA) works to improve the lives of those living with hypertrophic cardiomyopathy (HCM) to prevent untimely deaths and advance global understanding. They provide support, advocacy, and education to patients, families, the medical community, and the public about hypertrophic cardiomyopathy, while supporting research and fostering the development of treatments.
Helpful Tips
The HCMA Lori Fund will provide micro travel grants to HCM patients traveling to an HCMA-recognized Center of Excellence for care or for HCM patients traveling to a facility for heart transplant care.