I never had it explained to me either so my one and only flare I had recently took me by surprise. Can anyone tell us how to consult our Rheumatologist and how to describe our symptoms? I realize everyones symptoms are different but there has to be a better way to describe pain other than a scale from 1-10.

Mine too! Only had to add prednisone after switching meds. Started with methotrexate, then Remicade infusions, then Arava, then Xeljanz, now on Orencia. Had to do a prednisone burst in between each change. Fingers crossed.🤞

You should definitely call your doctor. Tell them where the pain is. Describe the pain. For me it is sharp sometimes throbbing pain.
Prednisone is usually the best thing for flares. You will learn it is a Love Hate relationship. Some people get “roid rage” some get lots of energy. I get hungry which sucks because I am fluffy already. If you are on it for a long time you will get a round face.
Hopefully this helps!

Are you able to contact your RA doc through the patient portal. I find it a valuable tool. I send my doc an update on flares, meds, and new side effects in the morning and usually have a response by the evening.

My doctor gives me a tapered prednisone as well.