My question is, I guess, do other people have similar
reactions to cortisone? I know that with MS, you sometimes have IV steroids as treatment, and wonder how that goes. I'm undx'd, so haven't had experience of that sort.
I had about 6 hours of sleep last night, so things are looking up! :o)
An interesting note; I have been having MS "hug" type symptoms for nearly two weeks, now, and it seems to have lightened up quite a bit since the epidural.