We have educated an estimated 1 million visitiors to our website, first launched in 1996 - making the HCMA one of the first patient advocacy websites. Our goal is to provide support, advocacy and education to patients, families, the medical community and the public about hypertrophic cardiomyopathy, while supporting research and fostering development of treatments. Here you will find information on how HCMA has buildt awareness globally and how we advocate for our HCM patients and families.