For which I am SO grateful. I thought that the steroids would just keep the pain at bay but after reading so much I realize that few people have been as fortunate as I am... although I am still at 10- 12 mg daily. I have decided I am not in a hurry to reduce. (My doc will be so pleased! As previously I have pushed to reduce faster!) After the 2 weeks of pain and hell in Jan when diagnosed, I have had almost no pain.
I have been fantastically exhausted, unable to work or focus, MAJOR sleep pattern disruption, was nauseated for 3 months, shakes, loss of appetite for the first month, now I'm starving...(especially for SALT, lately... never used to care for crisps -potato chips, right? - and now I crave them!! ) Emotional, memory issues, irritable, shaky, GERD, thinning dry skin, hamster cheeks, dry eyes, nightmares, sensitive teeth, NEVER feeling that I've had enough sleep regardless of how much I did have... but, rarely pain. I am tired pretty much ALWAYS. Over the past couple of weeks, I feel back/hip pain but it is not debilitating - in fact, its not bad compared to my baseline prior to diagnosis. I don't know if this would be considered a flare. I see my rheumy Monday and will ask for blood tests to compare... he sees me about every 6 weeks. We agreed that the steroid side effects were hitting me harder than the PMR lately, so we had a plan to reduce. I got nervous with the back pain returning so I changed it to every other day (10 then 12 ) until I see him. THoughts?