I wonder if anyone has the same experiences as I do, prior to Fybro flare my urine output slows and I start to become swollen (I also have psoriatic arthritis) in my joints, then my thighs, ankles and wrists. Then the pains.
I am really lucky as I have injections of 120mg Depomedrone twice a year, they last about 4 months then I have one month of oh oh here we go again then a month of Fybro pain and arthritis pain. Thee injections treat both Fybro and arthritis. My rheumatologist is lovely and keeps his eye on me ensuring that I have constant checks, he has tried other meds but I don’t seem to able to tolerate them very well, this seems the only thing that keeps me going.