Posted 4/22/2012 8:42 PM (GMT 0)
Hi Mayflower7, thanks for your post. I live in a small town and getting a family doctor is difficult so once you get one you stick with them....sucks but its better to have one then bounce between "on call" doctors, because at least you dont have to repeat everything to each new face. I did ask the specialist if RA would effect my kidneys and he said he didnt believe it could. I went for a MRI a year ago, and they said it did show some inflammation, and oh guess what you have a bad back and knees....(like I didnt already know that) lol. I usually have lotsa blood work done when I go see my rhuemy but that is only twice a year...she gets like 15 give or take tubes of blood.
They have not x-rayed my back where it is currently effected,because I didnt have that "idea" I thought it was an infection. It is in the lower back, where you would locate kidneys, on both sides. Mostly the left but also the right most days. My RA meds havent completely taken the pain, or inflammation away. I just assumed it would take some of it and that I had to deal with the rest. I was prescribed tylenol 3 for the pain, but it is just like taking m&m's or skittles ( with the added bonus of feeling kinda high , which really sucks) but no pain relief. Since the T3's dont work I did tell my family doctor how it worked now for me, and she upped my amitriptyline from the 25mg to 50mg daily hoping that would help and told me to just take advil for the pain....well that didnt work...still have pain and advil is a bigger joke than the T3's. (advil works for headaches for me but thats about it.)
I think I have alot to learn about RA, and am trying my best. Just frustrated I guess, and self diagnosing isnt working for my new kidney area pain and was hoping for some help. You all have helped alot, and your support certainly appreciated. Thanks again. Have a great day ((gentle hugs))