Merry Christmas, everybody! :sleigh:
...Jo, I had forgotten about the girl you trained that had the fusion. I needed a lift today! I'm hoping that with the fusion, I could at least go back to work part-time. Being a home-body isn't my "cup of tea"! (hee hee)
I guess I'll have to ask Dr. K why he uses a Kutcher nail as his first choice. I think that's what he said the "name" of it was, as well as the talk of "intramedullary" (wow..that's a mouthful!) verbage. When I had my second opinion last summer with another Dr., he told me he would use plates and screws. I think I've got that discussion on her somewhere! I definetely know that I don't want the rod that goes in through the upper femur/hip area. Dr. K said he did not want to do that either. He had more successes with the (2) separate rods. In other news...............
John had to cut off the pink cast yesterday. Can you believe it! It became so loose, that I could slide it up and down a good 5 inches, and get my hand in from the top enough to touch the bottom of my kneecap. Because it was so loose, I could bend it a good 15-20 degrees inside the cast. NOT what this cast was supposed to do. It was supposed to be ROCK SOLID. hhhmmm....is it just me???? Why can't thinks go smoothly and correctly! Sooooo frustrated. Anyway...I'm using the cast I had this summer with the velcro straps to secure it tight. I can take it off at night, or anytime I want, but I'm going to keep it on just as if it was the pink one.
Jo...do you know the hospital time involved in a fusion? He also said I'd need a blood transfusion. Do you know the recovery time when they use the nails/rod? Would I be in a cast afterwards? .....my mind is mush....lots of information to remember and retain.
He doesn't think that the fusion will take away the pain, as it's RSD/CRPS and nerve, tissue and muscle related and not so much the knee implant itself. My PCP believes the same. So...the main reason for having the fusion is to stop the knee from moving and causing the pain, AND for stability to stand, "walk" and try to have a normal life without looking like a hunchback and grabbing at furniture just to go from one place to another. Bottom line: movement makes the RSD flare up and get worse. So...stop the movement and maybe the RSD will subside to a minimum instead of rearing it's ugly head each and every day to a pain scale of 6 or more. I can only hope!!!!!! I know I don't have many options left, and this is the one that I'm comfortable with and believe I can live with. Amputation is not an option. I just can't do that.