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Multiple Hereditary Exostoses
Websites
Support for families affected by this rare condition.
http://www.ox1.co.uk/hmesg/index.html
A personal family study about MHE and its occasional connection to the cancer chondrosarcoma. By a woman who has lived with these conditions for 54 years.
http://members.tripod.com/MOONROSE_22/index.html
Information about multiple hereditary exostoses (MHE), a bone disorder. Includes links to a support group.
http://www.radix.net/~hogue/mhe.htm
Bill's personal web site with links to a chat page, an email list with 60 members, and a message board.
http://www.angelfire.com/il/Dukett/MHE.html
The Bumpy Bone Club is a support group for kids with multiple hereditary exostoses and their families. Includes personal stories by affected children.
http://www.geocities.com/mheandme/
Organization formed by representatives of several existing support groups for individuals and families affected by Multiple Hereditary Exostoses.
http://www.geocities.com/mhecoalition/
From online orthopedic textbook.
http://www.wheelessonline.com/o6/96.htm