Have been to rheumie appointment this morning and she has suggested Methotrexate by injection as was making me feel sick in tablet form. Anyone have any experience of this? My symptoms are getting worse and seems to be very much a combo of Lupus and Fibromyalgia. Am very shaky and wobbly until later in the day when have had another nap in the afternoon. Am very sadly now looking at retirement due to ill health so this year looks to be one of some massive changes, as money will now become very scarce! Am also being referred to psychology service to someone who has worked with other Lupus patients so have some hope that I will find some degree of peace. It has taken about a year and a half to get this far so i would say to others don't give up keep pressing for what you think is right for you....even though it is exhausting and draining.