Welcome to the Juvenile Scleroderma Network, Inc. (JSDN)
A support network helping children and their families with
juvenile scleroderma
The JSDN is a volunteer staff made up of volunteer parents, health professionals, and people interested in Juvenile Scleroderma.
Founded in 1999, the JSDN is the only national voluntary organization that works exclusively for children affected by Juvenile Scleroderma, and their families.
Our mission is to provide emotional support and educational information to parents and their children living with juvenile scleroderma; to support pediatric research to identify the cause and the cure for juvenile scleroderma; to enhance the public's awareness of juvenile scleroderma and related diseases.
Awareness,
Support,
Research...CURE
Together let's keep the milestones growing until there is a cure!
Juvenile Scleroderma Research.
Help JSDN support juvenile scleroderma research, today!
Because Kids Get Scleroderma, Too!!!
As part of their pioneering research into the genetic and environmental risk factors that may result in an autoimmune disease, the National Institutes of Health is seeking research subjects from the JSD community. Click here to see how you and your family can help.
What if Juvenile Scleroderma Network earned a penny every time
you searched the Internet?
Well now we can!
Goodsearch is an easy way to help the Juvenile Scleroderma Network through a new Yahoo!-powered search engine and online shopping mall called
GoodSearch.com.
The more people who use this site, the more money will go to the Juvenile Scleroderma Network. So please spread the word to your friends and family.
http://www.goodsearch.com/?charityid=330644.
On January 13, 2007 and August 21, 2007 the JSDN was featured as
Charity of the Day!
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