WEBSITES & BLOGS
More to come
The Sjogren's Foundation (SF) is the go-to resource for reliable, up-to-date information about Sjogren's. The amazing staff, and wonderful experts on the Medical and Scientific Advisory Board work on our behalf. Take time to explore the website, . Check out the patient education brochures, conference CDs and many other resources. If you have not already joined, it is truly worth it. We are fortunate to have such a talented, hardworking, professional organization. As you can tell, I['m a proud member and a big fan!.
A wise and wonderful blog by Janet Church, Sjogren's patient and Chairman of the Board, Sjogren's Syndrome Foundation
"Those of us that live with an autoimmune disease (I have Sjögrens) fight daily to have fulfilling and productive lives. Sometimes it works and sometimes it doesn’t. This blog is a place where I can share my experiences living with Sjögrens, and share what I learn by being part of the Sjögren’s Foundation. My goal is to help the readers live each day a little bit better." ~ Janet Church
3. Neuropathy Commons
Excellent resource for Sjogren's neuropathy, and neuropathy in general, from Massachusetts General Hospital.
Link to new page.
More to follow!