This site is dedicated to Courtney, a very sweet, vibrant little 9 year old who has had MSUD since birth. Courtney's story inspired me to build this site so that I may be able to spread the word of this devistating disease and educate those [like myself] who had never heard of it, and help in the research, treatment, and possibly one day -- a cure for it. I am doing this for Courtney and for all the other precious children who are a victim of this disease. Anyone can find the definition of MSUD, if they hear of it and do some research, but the children need to have a way to tell "their story". The fear, pain, struggles, hopes and dreams of these children have more of an impact than any medical term could ever tell. Courtney's own story can be read at Courtney and MSUD.

Follow the links below to find out more about MSUD, visit my chat room, and to enter my forum discussions. The link will take you first to my rules page for posting messages and using the chat room. After you read the rules, you can click on the link to go where you want.

Thank you for visiting.
Bright Blessings
Ariadne

Courtney's Own Story
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You are visitor number since January 18, 2001

Last update - February 19, 2000

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