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The internet is a big place. There is a lot of information out there. Some are very, very good, and some are very, very bad. On this and the linked categorized pages are some web sites we have found useful.



b-auto.gif - 4.19 K Autoimmune Diseases. The internet is a big place. There is a lot of information out there. Some are very, very good, and some are very, very bad. On this and the linked categorized pages are some web sites we have found useful.

b-medical.gif - 2629 Bytes Medical. Autoimmune diseases are diverse. It is difficult to describe all the symptoms possible. On these pages we have tried to include a bit of everything you might expect from scleroderma and the other autoimmune diseases. There are so many wonderful, informative internet sites out there. These are but a few that we have found to be useful.

b-support.gif - 2660 Bytes Support. No matter who we are, patient, caregiver, family or friends of patients or caregivers, we all need support. We need to know there is always someone there to talk to, to lend a helping hand, to lean on, to just plain listen, to know we are not alone. There are individuals and groups worldwide offering this help.

b-family.gif Here are our family pages. Our SD World family and their families. Right now we are featuring our Furry and Feathered Friends. This is also the place for bragging about our families, be they human or otherwise!

b-nutrition.gif - 3643 Bytes Nutrition. We all know that diet and nutrition are important. But, if you have a chronic illness, you know you have to watch almost every bite you eat. You need to know the best from the worst, what you can eat and what you cannot. Hopefully, these links will help.

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Just for Fun. It's play time! We all need a little "play" time. A chance to kick back and enjoy ourselves, right? Of course! Here are a few "fun" places.

b-atoz.gif - 4.02 K Shelley's Scleroderma From A to Z, "Whether you are a patient, caregiver, or medical professional, we can help you find the information and support you need to deal most effectively with the many challenges of Scleroderma."

b-swa.gif - 2368 Bytes SWA...The Scleroderma Webmaster's Association. "We help Scleroderma site visitors readily find the Scleroderma resources they need by joining all of the SWA web sites together via a hyper-linked logo to a list of all SWA members. This makes it quicker and easier for people to find Scleroderma information on the Internet."

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