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.
You can help us
The
Still's Foundation is keeping track of individuals who have been diagnosed
with Still's Disease. This information will help us in our efforts
to raise awareness in the medical community and to promote research on
Adult Still's Disease.
Since
we are a non-profit organization we rely solely on donations. If you
would like to make a donation to the Foundation please contact Carole
Whaley
You can
also help us raise funds when shopping online at Amazon.com. Amazon
will donate a portion of every sale that is generated from the links of
our website. To shop at Amazon and help our
foundation please visit Amazon through our BookNook
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.
Click
to subscribe to stillsdisease
would
you like to meet the Members of the Support Group
Join our
Weekly Chat !!!
Please Join us For
our Weekly Chats Each Thursday Night at 9:00 PM EST
Click
here to Chat
StillsNet
StillsNet
is a publication of the latest news and research on Still's
Disease, Rheumatoid Arthritis, Osteoporosis, Fibromyalgia, Medicatins, and other Autoimmune diseases relating to
arthritis
Click
to subscribe to StillsNet
If
you have any problems subscribing please contact Jennifer
To
view past articles click here
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
Sign
up here for the Conference
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!
Click
here to subscribe to JRA-list at Yahoogroups
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.
This site was last updated
March 15, 2001
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Our Guestbook View
Our Guestbook
This website is dedicated in memory of Carol Orr, 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
Webmaster@stillsdisease.org
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