Our founders have given us a dedicated site for Sjogrens. JC has gathered some great info for us. Please join us there. Sjogren's can be much more than dry eyes and dry mouth!
Hi Susan,
Nice Discussion for the new site for sjogrens's syndrome
http://www.sjogrenssyndromesupport.org/
I know this syndrome is a pure nightmare to me alone.
Love Terri xxx
Thanks Terri, I just finished posting a new discussion there, found a link to some great info written by an MD. I have learned so much about this disease since joining Ben's Friends, and much of that good info came from you, Terri!
Hope you are having a good day!'
Big hugs,
SK
Hello Susan,
I'd love to join the site but like yourself my head does'nt allow me to multi task sites and besides Lupus, sjogrens is a main issue with my health alone as you know...i'd join today if i was'nt with the fibro.
I can't help how my head works and don't forget i have'nt got the full marbles mate to match the whole of my brain.
Hug your way Terri xxx