The MHE Research Foundation is a nonprofit 501© (3) organization for the support of researchers, families & physicians dealing with (MHE) Multiple Hereditary Exostoses (MO) Multiple Osteochondroma a rare genetic bone disease.

The MHE Research Foundation Five point mission is to REACH, advance and support the following.

RESEARCH, to help researchers one day find a treatment / cure for MHE. Our foundation works hand in hand with researchers from around the world on this mission.

EDUCATION, to provide clinical informational guides to help benefit both families and physicians.

ADVOCACY, bring awareness about this disease in all areas throughout the world.

CLINICAL, to help provide resources to families enabling them to find the medical care they need.

HOPE, is that the research being conducted on MHE, the informational resources will bring a better quality of life to the families affected by this disease.