Hi there.
I def have symptoms of nerve root compression esp the altered sensation. I used to get pins and needles and numbness alot, also pins and needles in groin area but that resolved itself. No change it bladder/bowel function though I did have a fright a few months back when I had the sensation of a full bladder but unable to urinate and had to sit for around 5mins or so before bladder would empty. This was put down to the codeine and also due to the fact that I was getting constipated, again due to the codeine. I now make sure I drink plenty water and this is all ok now. Re the altered sensation, my foot still goes numb and I get an odd thing happening when I walk sometimes. It's very weird. Normally you don't have to think about moving your leg yeah, you just do it. Well sometimes it was like it took all my concentration and will to be able to move my leg to walk. It wasn't paralysis as I could feel my leg no problem and it did move no problem,it was just that I had to conciously really think to move it. Most odd feeling. The chiro explained why that happened and it made sense, can't remember exactly what he said but it was something to do with the different kind of sensory nerve cells being effected. I also have muscle weakness in my foot and I did lose my ankle reflex at one point but it seemed to come back again and I did wonder if the Doctor who tested my reflexes at that point was just not very good at finding them because the Chiro was able to get it straight away.
Yes, the recurring flare ups are acute in nature and always seem to occur a few days after over exerting myself or walking downhill. Suggests to me that this is due to inflammation and swelling building up over the course of 2-4 days as the flare ups never occur until after a few days of over activity.
The Chiro has said that the SI problem needs to be sorted or else the disc problems and other back problems will keep reoccuring. He also said that I have a slight lumbar lordosis. Funny that cos I always wondered about my shape as my bum always seems to stick out too much and my belly is always protruding too much also (and it's not fat cos I'm slim!!) He also said that my upper spine was flatter than it should be. I think the main aim of his treatment is to get my spine and pelvis moving properly and to alter the shape of my back. Certainly, my back looks different to me when I look at it in the mirror. He says that I have problems which won't be corrected overnight. With you saying that the treatment is different for nerve compression and nerve sensitisation I wonder if the Chiro has been treating me differently as I had told him that the nerve was NOT compressed as that is what my GP had said to me.
Re Neuro Linguistic Programming, it is something I've heard of, sound interesting and my mother has just bought a CD about it as she is very interested in finding out more about it to help her, as she has Fibromyalgia.
Multifudis is the deep muscle in the back right? When I used to do Pilates I just bought a pilates video and did that and it seem to help my core but I do wonder if I didn't do things properly and possibly set myself up for future trouble. The Pilates type breathing that you have to do, I find very difficult. The Chiro has given me a static abdominal exercise to do. Hard to explain but you pull in the muscle just above the pubic area but you don't hold your breath but keep breathing in and out whilst just pulling in the muscle here. And you feel a tightning there and also a tightnigh in the mid back. He felt that I wasn't ready for any non static abdominal exercises. But for the past week I've been doing Pilates type sit ups where you flex your knees and hips at 90degrees and just lift your upper back slightly off the floor and it is causing no pain to my back or down leg but maybe I should stop cos there is always the possibility that I'm not doing it correctly.
I would like to go back to see a Private Physio but at the moment I just can't afford it as I'm not working. The Chiro is giving me treatment at a reduced price as I'm unemployed and I have a membership to a Health Trust which pays for half of the treatment. But yes, I'm quite worried that if I did decide to go for surgery that it wouldn't resolve my pain but at this point I do feel like I'm running out of options. As for the Cortisone injection I'm only going to get one. I'm of the school of thought that thinks that too many can weaken joints in the long term. And I do also believe that inflammation is part of the healing process and shouldn't be supressed but I'm getting to the point where I'm desperate to get my life back!
PS - I'm in Angus area in Scotland.