Hi everybody, back from my hols last night. Weather was scorching! so spent most of the time under parasol, because of mycophenolate. Now it is back to reality and a round of hospital appts, one this week. been reading posts, noticed comments about night sweats etc, yes I have them through the night and during the day, not hormonal, I am going to ask the consultant if it is a symptom or medication. I also get tingling in legs, sometimes I want to scratch them but I know this will only make it worse!! There are so many symptoms with systemic sclerosis and raynauds, that I lose count, and I really try to lead as normal a life as possible, sometimes pushing myself to far, but I think stubourness runs in the family! Its just getting the balance right. I have to admit I get fed up with taking so much medication and it doesn't help I am on anti depressants because of the repercussions of divorce! Anyway this is a great place for support and giving support.