Went in Monday for my 3-month check up for my second knee. Would not have gone in if I wasn't having issues, but I'm having issues. The only time I don't have a burning, stretching pain around the top and sides of both knees is when I'm reclined and not moving my legs. At almost 8 months out from first knee and 5 months out from second, I know that's not typical. I'm still taking Norco and extra strength Tylenol to control the pain, and Celebrex for the swelling. It has only been two weeks since I've been off the assistance of a walking pole. I've had too much pain and stiffness to walk on my own. Buy my quads/hams/glutes are finally built up enough to support me.
When doc examined my knees, he commented about the amount of swelling and the color of my scars - still very purple - and how the skin around my knees is different than my other skin (wrinkled like an elephant's) and the capillaries are showing (red dots all over). He said that was an indication of the healing inside, which is not healing. He asked me if it still hurt to have items touch my knees. It does. When I'm home I have my pant legs rolled up much of the time because it's irritating to have material touch them. I also get pain in the back of my knee sometimes, more of a pushing pain that comes and goes. He said he would be concerned that I had an allergic reaction to the metal if I were running a fever, but I'm not. He also said the implants he used (Smith & Nephew Journey II) are hypoallergenic so he wouldn't expect me to have an allergic reaction.
His diagnosis? Complex Regional Pain Syndrome (CRPS). I'd never heard of it before. He prescribed a Medrol does pack (oral cortisone steroid, which I will not take because the cortisone injections in my knees before surgery caused major flares that lasted for weeks), Lyrica (Gabapentin makes the world spin around me), and Elavil. I'm happy to say that the pain is now gone; I'm left with the stretching feeling, but I'll take that over burning pain any day. After doing a bit of research on CRPS I learned that some people recover from it, and some don't. I'm hoping and praying that I'll be among the percentile that heals. I would hate to have to take these meds for the rest of my life!
Just wanted to share about my CRPS in case someone else is way past their surgery date but is still having a lot of pain and/or swelling. You're not being a big baby or imagining it. We know it's real!
I'm in the process of reading Josephine's and others' posts on Bonesmart about CRPS.
