Rheumy said I had slight protien in urine at my last appointment in December, plus blood tests showing raised levels of disease activity. I have now been asked to provide another sample for retesting, & measurement of creatinine levels.
I would be interested to hear everyone's experiences on this. Can the protein levels fluctuate, like the disease itself does? At what point is treatment altered to address this? I've read the relevant info on Lupus UK & St Thomas's site. But you, my fellow lupies are always so much more helpful, & explain things in plain English.