Multiple Hereditary Exostosis (MHE)
Who to Contact
8838 Holly Lane
Olmsted Falls, OH 44138-2701
The MHE Coalition was formed to provide support and information to people living with Multiple Hereditary Exostoses ("MHE") and to reach out to MHE-affected individuals and families throughout the world. Our organization is dedicated to promoting and encouraging research to find the causes, treatments, and ultimately the cure for this rare bone disease.
Where to Go to Chat with Others
- Hereditary Multiple Extosis
A place for friends to gather and talk about HME.
This forum allows MHE-affected individuals/families to share their knowledge and experiences. MHE affects each person differently. Postings reflect a wide range of experiences, many of which may or may not affect you/your child/or family.
- MHE Xray Sharing Group
This group enables people with multiple hereditary exostoses (MHE, also known as Osteochondromatosis or Diaphyseal Aclaisis) to share images from
Xrays, MRI scans and so on. It is also intended to provide a place to share details of treatments and symptoms.
Learn More About It
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