Hi im fibrolady37 & i posted not to long ago asking if anyone has sygrens syndrome. I got a lot of replies & id really like to hear from any sufferers to keep in touch with. My skin is so dry in the hot sun i have to put rehydrating cream on my whole body all day & night. Which is really hard because i got diagnosed with arthritis a few weks ago & the pain is unbearable its really getting me down big time. Im really looking forward to mailing other sufferers to see if we can help each other. Take care Fibrolady37.