Whilst being very conscious of the problems with getting elective surgery back on track at the hospital, I was getting a bit concerned I’d dropped off the system and so have followed up a few time over the last 2 or 3 months to see what the MRI showed, and what the next steps will be. At one point I was told that Mr Mundil needed to review the MRI to make sure there was space for the SCS before booking me in for surgery. I pointed out that I hadn’t actually seen him in person yet, and he had said he would need to see me in order to determine where might be the right place to put it to get the best affect. The next time I was told the MRI results were being reviewed the following day and I would then get an appointment. After a few weeks I still hadn’t heard so I chased again. A few days later I received a copy of the clinic letter describing the discussion I’d had with Mr Mundil back in September.
I’ve now had a follow-up appointment to see Mr Mundil in person. It’s not until July, but at least I know things are moving. I’ve got a growing list of things to ask him before making a final decision, but having considered a number of things, and done more background reading, I’m feeling inclined to go with the more invasive surgery, but will obviously see what his answers are to my questions.