International Still's Disease Foundation

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Welcome to Stilligan's Island

 

Still's Disease is a rare and often misunderstood disease which
strikes both children and adults

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.

Check Out What's New on The Website

    

index.1.jpg (786 bytes)    Our Support Group     index.1.jpg (786 bytes)

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. 

Please join our support group's mailing list

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would you like to meet the Members of the Support Group

or

View The Support Group's Calendar of Events

Preview This Clip Now!

Join our Weekly Chat !!!

Please Join us For our Weekly Chats Each Monday and  Thursday Nights at 9:00 PM EST

Click here to Chat

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index.1.jpg (786 bytes)   StillsNet   index.1.jpg (786 bytes)

StillsNet is a weekly publication of the latest news and research on Still's Disease, Rheumatoid Arthritis, and other Autoimmune diseases relating to arthritis

 


Click to subscribe to StillsNet

If you have any problems subscribing please contact Jennifer Jay

To view past articles click here

 

Do you have any questions about Still's Disease? 

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You can post them at our Message Board

 

    The First Annual Still's Disease Conference will be held in Las Vegas, Nevada, October 2001

Sign up here for the Conference

We will be posting more info at a later date

index.1.jpg (786 bytes) Caregivers of those with JRA index.1.jpg (786 bytes)

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!

Click here to subscribe to the Systemic JRA Egroups

Visit Georgina's Systemic JRA Page

Also Check out JRA World

 

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

 

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          This site was last updated

July 10, 2002

 

 

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Sign Our Guestbook     View Our Guestbook

 

 

 

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        This website is dedicated in memory of Shelly Himes-Graffeo and Kate Frost. We miss them dearly

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index.1.jpg (786 bytes)   Website Design by Jennifer Jay   index.1.jpg (786 bytes)

Any questions or suggestions concerning this website should be sent to

Webmaster@stillsdisease.org

 

We Subscribe to the Principles of Health On the Net Foundation

   

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DISCLAIMER:

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