I received my results from some of the blood work I had done. I’m still trying to figure out why I have such excruciating back pain. So far, I have no answer. I usually don’t get relief from the pain pills better than a 6 on the scale of 1-10. I have to wait until I get a little relief to be able to go walking, and it’s a catch-22, because that’s when I get the most comfortable, when I’m walking! It’s an odd situation! I spend a lot of time being extremely frustrated by this, as most of you know all too well how that feels. I don’t let it stop me from doing what I want to do, but I really have to muster my motivation to get through it. Every single day! I thought that I had experienced the most pain I ever could have felt before with my MS, but this is a whole different animal.
I have researched the connection between ms and back pain extensively. My neurologist said she doubts that it is because of the ms. But really there (so far) is no answer. Any ideas, my friends? Thank you so much 😊. Love to you all, Kelly