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A Support Group for Kids with
Multiple Hereditary Exostoses
and their Families
MHE and Me is a proud member of
THE MHE COALITION |
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Whether you are a kid with MHE looking for new friends who understand what it's like to live with bumpy bones, the family of a child with MHE looking for information, or a medical provider trying to understand some of the life issues faced by your MHE patients, this site was created for you! MHE and Me was started in July 1999 and the web site has grown beyond our wildest expectations, with children and families from throughout the world contacting us. We continue to give kids a place to express themselves through their writings, poetry and art, and we also continue to develop tools to help families deal with medical and school issues. We decided that it's time to give MHE and Me a new look, and reorganize the web site to make it easier to navigate. My daughter, Nicole, who was the inspiration for this group four years ago, designed our new artwork. As a fourteen year old MHE'er, she understands what it's like to juggle life with MHE, and she did a great job expressing it in pictures! We hope you enjoy the "new" MHE and Me. Please let us know how you like it!
Susan Wynn, Co-founder, Director & Webmaster
mheandme@yahoo.com |
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The Bumpy Bone Club
Stories, Poems, Essays and Art Work by Kids and Teens with MHE |
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The We Care Corner
Writings, Poems and Art Work by Family and Friends |
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Grown up MHE'ers
Share Their Bumpy Bone Stories and Advice |
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MHE and ME Resources
MHE Kids & School (Tools developed to help
explain and obtain needed accommodations)
MHE Kids & Doctors (Tools developed to help keep track of bumpy bones, doctor's appointments and surgeries, and pain) |
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MHE Links
Sites to help your child cope with chronic illness, teasing, depression, chronic pain and other issues; MHE organization links; Helpful products recommended by kids and parents |
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Prior to our site makeover, MHE and Me received over 9,000 hits! |
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DISCLAIMER
While many find the information and experiences that we share helpful, it is in no way a substitute for professional medical care. Our support network does not engage in the practice of medicine. In all cases we recommend that you consult your own physician regarding any course of treatment or medicine. |
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MHE and Me Privacy Notice |
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