VISIT TO OS 8 JULY
INVESTIGATION: First off he asked how my knee was prior to surgery. I explained that it had been OK, but two severe pain attacks prompted my visit to the OS, where he diagnosed bone on bone hence the TKR.
He examined my Xrays. Prosthesis looked good. He said it wasn't the type he would use, but that was just a matter of preference. He then felt my knee to see if it was unduly hot (checking for signs of low grade infection). It wasn't. He asked if I was allergic to anything (checking for metal allergy). I said No. Then on to questions to do with pain. I explained I had no pain/discomfort when off my feet. That I got a lot of discomfort when walking. That it felt like I had a tourniquet around my knee. I was then led to a bed where he checked how flexible my knee cap was. He said it felt good. He checked my bend. NOT GOOD. Only around 100/0. He asked me to walk for him. It showed I had no limp. He said he didn't use MRI scans because of the metal. He did a CT scan. From the CT scan, questions and examination he said the problem was EXCESSIVE SCAR TISSUE.
WHAT TO DO ABOUT IT. He outlined the options 1. MUA 2. open surgery to remove scarring 3. keyhole surgery to remove scarring . He said all of them came with a high risk of making things worse. The reason being that if a patient is prone to excessive scarring all 3 options could result in new scarring forming.
CONCLUSION. He said given that I didn't have pain, but chronic discomfort. That my bend was above 90/O. That I didn't have a limp, didn't need a stick or pain meds, that he didn't want to do anything now. He said there was a reasonably good chance that given more time the scarring would decrease on its own. At the same time I would get more used to how it was. I asked about more PT. He was somewhat indifferent. He didn't say as much but I got the impression he thought it was a bit of a waste of time. He did however say that I should live as full and active a life as possible. He said any improvements from now on would be incredibly slow. For this reason he said he would see me again in 5 months time. If things had improved, the waiting would have been worth it. If things had not improved or got worse then we would need to review the options.
HOW I FEEL ABOUT IT. I've mixed feelings - pleased that there is a chance that I might not need further surgery. Sad because I have to continue living with chronic discomfort and uncertainty. The goal posts have been moved yet again. I am nearly 17mths post op, by the time the OS sees me again I will be 22 mths post op. When I look back at some of my early BS posts, and I asked how long will this take, I never imagined I would still be asking the same question at this stage of the game. I have to get on with it. I have no other choice. So come tomorrow I will dry my tears and put my best foot forward.
POSTSCRIPT I Never could have coped without the kindness, help and support (and love (Diana)) that Bonesmart has given me. Thank you all from the bottom of my heart. Carol