Guest guest Posted September 26, 2006 Report Share Posted September 26, 2006 I thought I had true acceptance of my illness, but I am finding that I still have been in denial or not sure exactly what to call it. I had a rheumy follow up to get some test results, since I cannot seem to get a right medicine combination and still in constant pain with my sed rate still soaring and lower back pain, that even with increasing excercise/stretching and desparately trying to lose weight, their is pain. Ok, yes I need to lose weight, but there is a pain that even if I was a size 2 would still be there I know, it. Today, I somehow feel very mixed, since I have extreme inflammation of my SI joints, spinal stenois,and degenerative disc disease. Also, in addition of PA and Fibro, I have the markers for RA now as well and my sed rates are higher than I was just 3 weeks when I was there last. So, I knew I had something wrong in my back, but ok, wow. So, my insurance copmany approved the increasing of Humira to every week, which I can barely stand the thought of, since I have no one to help me out. The thought of that shot every 2 weeks makes me cringe, I just cried leaving her office, since the feel of that shot is ugh........ Ok, I am having a pity party today, sorry........Plus, all the meds I was given, to help with pain, I really cannot even take, since I am lucky enough to still be able to work, but I would never get up ontime. So, I will figure something out since I cannot sleep, ugh what a cycle..... Thanks for listening, Debbie [Editor's Note: Debbie, be sure to let the Humira come to room temperature before injecting. I also found it very helpful to " freeze " the injection site for several minutes beforehand (I used a box of frozen peas, but you can use an ice pack, LOL). It was also a lot less painful to inject very, very, very, very slowly. By doing those three things, I eventually found the Humira injections to be quite tolerable. Have you talked to your rheumy about switching to Enbrel? It's a lot less painful on the way in. Kathy F] Quote Link to comment Share on other sites More sharing options...
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