International Still's Disease Foundation
Welcome to Stilligan's Island
Disease is a rare and often misunderstood disease which
The International Still's Disease Foundation was founded in the spring of 1999. We wanted to bring together those who have been diagnosed with Still's Disease and provide them with support, information, and a chance to meet others with this disease.
Our Support Group
Our founder, Tom Kufahl, created a mailing list for those with Still's Disease to communicate. It has become the "heart" of our support group. We encourage you to subscribe to the mailing list. From there you will be able to email every person on the mailing list. It is a wonderful source of support and information for those who are newly diagnosed. It gives you a way to ask questions, tell your story, or if you need a friend.
View The Support Group's Calendar of Events
Join our Weekly Chat !!!
Please Join us For our Weekly Chats Each Monday and Thursday Nights at 9:00 PM EST
StillsNet is a weekly publication of the latest news and research on Still's Disease, Rheumatoid Arthritis, and other Autoimmune diseases relating to arthritis
If you have any problems subscribing please contact Jennifer Jay
Do you have any questions about Still's Disease?
You can post them at our Message Board
The First Annual Still's Disease Conference will be held in Las Vegas, Nevada, October 2001
We will be posting more info at a later date
Caregivers of those with JRA
Do you have a child with systemic JRA? Georgina (Josh's mother) has created a mailing list for especially for the parents. She has also made a website for systemic JRA and it includes a history of her son's experience with Still's Disease. It is a wonderful website with a lot of information so make sure you get a chance to visit it!
This website was created to provide as much information about Still's Disease as possible. You will find helpful medical information such as a guide to lab tests, guide to medications, alternative therapies, the latest research on Still's and other related autoimmune diseases. The site is frequently updated so please be sure to visit often.
And don't forget to visit The Original Still's Disease site
This site was last updated
July 10, 2002
This website is dedicated in memory of Shelly Himes-Graffeo and Kate Frost. We miss them dearly
Website Design by Jennifer Jay
Any questions or suggestions concerning this website should be sent to
We Subscribe to the Principles of Health On the Net Foundation
The materials and information on this server are intended for educational and informational purposes only. The materials and information are not intended to replace the services of a trained health professional or to be a substitute for medical advice of physicians and/or other health care professionals. The International Still's Disease Foundation is not engaged in rendering medical or professional medical services. You should consult your physician on specific medical questions, particularly in matters requiring diagnosis or medical attention. The International Still's Disease Foundation makes no representations or warranties with respect to any treatment, action, application medication or preparation by any person following the information offered or provided within this website. Any information used from other websites was done so with permission from each site, with an exception to those of "public domain", whereas we believe any site without a cited reference was a "public domain site" and for our use. The International Still's Disease Foundation is a non-profit organization. This page was last updated on June 13, 2002
Copyright© 1999-2002 International Still's Disease Foundation