The MHE Coalition is a 501(c)(3) non-profit charitable organization dedicated to finding ways to help improve quality of life of those living with Multiple Hereditary Exostoses/Multiple Osteochondromatosis.
The MHE Coalition
The MHE Coalition
- Develops resources to create a better understanding of MHE and the challenges that it may present, including chronic pain and fatigue, educational and work-related issues, surgery tips, and more. In addition, the ABC’s of MHE, written by some of the top orthopaedists in the U.S. treating the disorder, provides a comprehensive look at MHE, how it can affect each part of the body, some of the corrective surgeries used in treatment, physical therapy, and more.
- Provides gift packages to children undergoing surgery and their siblings, and helps empower children, teens and young adults through the Bumpy Bone Club.
- The Tom MacDonell MHE Scholarship Fund is offered to first year college or trade school students by application.
- Through our website, Facebook groups and annual gatherings, people can find support and information.
Please make checks payable to the MHE Coalition and mail to:
Susan Wynn, MHE Coalition, PO Box 651, Pine Island, NY 10969
or
Donna MacDonell, MHE Coalition, PO Box 128, Willisburg, KY 40078
Your donation is tax-deductible as allowed by law, and your support is greatly appreciated!
Susan Wynn, MHE Coalition, PO Box 651, Pine Island, NY 10969
or
Donna MacDonell, MHE Coalition, PO Box 128, Willisburg, KY 40078
Your donation is tax-deductible as allowed by law, and your support is greatly appreciated!