|LEARN ABOUT HCM FROM THE
HYPERTROPHIC CARDIOMYOPATHY ASSOCIATION
The Hypertrophic Cardiomyopathy Association was formed in 1996 by HCM patient Lisa Salberg following the tragic death of her sister, Lori, from HCM. The loss of several family members, along with the difficulties faced by the family in obtaining proper medical care, spurred Lisa to form the HCMA as a 501(c)3 nonprofit corporation, dedicated to helping the thousands of other families around the world facing similar issues.
Today, the HCMA functions under the direction of a medical advisory comittee consisting of physicians from the top medical institutions around the globe, along with a committed board of directors, a dedicated staff and enthusiastic volunteers.
The HCMA has helped thousands of families improve their lives and learn to live well with HCM; it has helped untold numbers of medical professionals become better educated about hypertrophic cardiomyopathy; and it continues to spotlight HCM and bring it to the attention of millions worldwide.
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