After posting here last week and having some truly remarkable support responses, I visited my rhumatologist. Right away she stated she had been considering my history/presentation and has come tothe conclusion I have Rhupus. I was still garbled with confused thoughts, headache and balance issues ect....so probably not one of the best days for me to see her. Upshot is, she's taking me off Methatrexate and putting me onvsomething stronger? Cant evenbremember the name of it and am awaiting a call from the rhum nurse to arrange it. As usual, taper down steroids once the new med is in my system. She is also giving me a pack of steroids for home to take right away when I know I am flaring. I have looked on the internet about Rhupus but not a lot there so would truly appreciate any info from this lovely community x
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