Change of Office Hours 
                                  With effect from 1 Dec 2010, Lupus Association's new office hours are as follows : 
                                Monday to Friday 12.00 – 5.00 pm 
                                 Please do not hesitate to contact
                                  us for further assistance. 
                               
                              Medical 
                                Welfare Subsidy 
                                We have now a firmly established 
                                welfare subsidy scheme. With rising health costs, 
                                many patients and their families are finding it 
                                increasingly difficult to cope financially as 
                                SLE is a long term illness and some drugs can 
                                be very costly, Do avail yourself of this scheme 
                                by informing your doctor or call us at 2549130. 
                                As the organization needs to be financially healthy 
                                for this scheme to succeed, we will also appreciate 
                                help in fund-raising efforts. Do inform us of 
                                any individuals or groups you may know who are 
                                willing to support us. 
                              Ward Visit/Handicraft 
                                Session 
                                Ward Visit is on Wednesday 
                                10.30 am, after which we will have lunch together, 
                                then move to the Lupus Office at Patient Education 
                                centre, Tan Tock Seng Medical Centre #B2/1/109, 
                                You are most welcome to come and join us. 
                              Mini-Library 
                                Books and educational tapes 
                                related to SLE are available. You can borrow them 
                              to increase your knowledge of SLE. 
                              Lupus Link 
                                Lupus Link also needs your 
                                support. Do share with us your experiences to 
                                encourage and build up fellow patients. You can 
                                use pseudonyms. We welcome all your comments. 
                                We will appreciate help in Chinese translation. 
                                  
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