LeeApril26 Those were my thoughts exactly about the CT scan. If I don't get better and better, I will definatley have it. It's worth the radiation risk. I'd rather risk that which I don't know will happen for sure, than live like this, which I know is a nightmare.
The OS said I can't get another shot for 3 months. I imagine there's a different protocol for hips and joints, as I've heard this before, but maybe he'd do it a bit sooner.
My next step would be the CT scan,
probably a blood test for metal allergy if the scan doesn't reveal anything,
consulting with the rhematologist, who wants me to go on methotrexate as he's suspicious I have sero-negative RA (I'm not so sure - my shoulders are better since I stopped paddling around the pool with only my arms - I'd think they'd still be bad if I had RA? and he's basing this on pathology report from THRs that showed 'synovitis' which is an RA thing - OS said he's seen it due to the inflammation from osteoarthritis, too, so...,
but instead of metho, maybe trying some prednisone by mouth for a month (oh boy, sleepless nights here we come!), and then - if there is no resolution
I suppose pain relief measures, like a pain clinic. That may be the only option if there is no diagnosis, and all else fails, as I can't live with pain and dysfuntion for the rest of my life.
Depressing....
Too bad your valerian isn't agreeing with you...I wonder if you take it with yogurt, or milk and crackers? Just a thought.
My muscles are flabby from underuse, and I am thinking of that, hoping I'll get back to being functional if and when I'm able to walk! I was in very good shape before all of this, but couldn't walk much for 4 mos before surgery, and had to modify the swimming. So it's been a while that I've been up and running like I used to do.
Thanks for the post. Are you still in Penna? The weather is definately better here, had some nice rain last night which we needed. I hope you're enjoying yourself and getting to the pool or the lake a little bit.
Any info or idea you have are always welcome, Lenora. You have a good thinking cap!
