Hi All, I am from Logan City in Australia. I have been dealing with Fibro for years now but only diagnosed last year after countless bloodtests continually bring up Lupas and then when tested directly for Lupas coming back negative, also always with inflammatory markers too high. Mostly my symptoms are pain in knees, sholders, hands, headaches extreme fatigue. I work 40 Hours a week in community housing as a Tenancy Manager and sometimes high stress situations. I use up more sick days then I earn lol. My Funding for position has been cut and my contract ends in July this year. I am thinking about taking some time to search for a Rheumotologist who can help me with pain management. I have been on Mobic, also antidepressent call Pristiq to assist me with coping with the stress management which seems to caused a lot of flare ups. sorry for rambling.