Welcome to the site. My name is Kathy and I have SLE Lupus. I live in the states, in South Georgia. I don't know how it works in foriegn countries. I am sorry to hear about your sister. I am wondering if maybe you could contact the American Lupus Foundation and maybe they could have some information for you. Maybe Saysusie one of the moderators of the site would have some information. Please keep posting and also post in the new members forum and thee you will get more replies.
Lupus for many years. Like most of my life. Sjogrens that started at 35 and Scoliosis, Spinal Stenosis, Degenerative Disc Disease, Osteo-Arthritis of the spine, Ankylosing Spondilitis, Periferal Neuropathy, mild CP and now just recently diagnosed with PA. I had a disc replaced in December of 2007.
Plaquenil, Sulindac, Imuran, Celiac diet, Tramadol and B12 shot once a month.