Alternative exercises if back extensions too painful?
Posted , 3 users are following.
Hi all,
Five months ago I prolapsed a disc at L5/S1, causing "partial compression of exiting right L5 root and compression of right S1 root causing radiculopathy". I received this official diagnosis from an orthopaedic consultant on 24 April as a result of an MRI scan I had on 30 March.
From my first ever appointment for this condition with a physiotherapist (which was late January this year) I had dutifully been carrying out my McKenzie back extensions as instructed by the physio, plus other pilates exercises as and when I felt able to do them.
However a few weeks ago I had a horrible, incredibly painful muscle spasm in my lower back which resulted in my taking a week off work and being unable to walk more than a few steps without significant pain. Now I feel like I'm back at square one - trouble getting comfortable sleeping again, can't walk more than about 100m without bad pain in my thigh and calf, can't bend to do shoes/socks/tights and so on, can't get out of bed without having to do some kind of sideways roll and hoping for the best! These are all the things I've seen a reduction in over the last few months and I was so hoping I was getting better.
Slightly worryingly, I've just over the last two weeks started to get numbness and pins and needles in my foot, along the outer side and in my three smallest toes. That's a first.
I'm on the waiting list for a cortisone injection (which might not be until August apparently) , but I want to keep up my stretching and exercises in the meantime. Question is, what do I do? McKenzie back extensions cause way too much pain as I can barely lie on my front without extreme pain in my buttock and back of thigh right now. All the research I'm doing is suggesting some kind of back extension and I just cant do it right now - I've considered loading up on the co-codamol & pushing through the pain but it just feels wrong in my gut, like my body is telling me not to.
This post has become much longer than I intended! I'm awaiting a call from my physio to get his opinion and hopefully an appointment but my PCT has a pretty poor physio department in my opinion, it'll be a month before I see anyone!
Any help or suggestions anyone can give would be so appreciated...I want so badly to get better and do all I can to heal, just not at the snail's pace the NHS seems to operate at!
With huge and sincere thanks in advance,
Nicola
0 likes, 5 replies
tara95293 nicola2312
Posted
its a shame you have had no responses as I am in exactly in the same boat. I see you r post was 12m ago. I would love to hear if you managed to get sorted as I just don't know what to do.
nicola2312 tara95293
Posted
So that's my experience. As you know when you're in chronic debilitating pain it's hard to think straight, let alone try and sift through all the stuff online trying to find that magic exercise that works.
I really really hope things improve for you soon, I really do - will cross my fingers for you!
All the best, Nicola
nixbadbax tara95293
Posted
I'm laid up in bed thanks to my ongoing back problems as I type this!
I hope I don't knock you with what I'm about to tell you, I will let you know what I've done and had done with the hope that you realise we are all different and what works for you, no matter what it is, is what you should do, no matter how mad it may seem.
I started with light moves, via Physio is always best, if not the internet will offer you basic instructions - cobra lift, child pose etc. Learn to listen to you body, if it hurts it tells you it's too much - keep it light and gradually move on. The key is not to aggravate but to gently place back into a less painfull position. You may feel a little sore but not more pain.
Ive tried all the reflex, chiro, TENS, alternative stuff, personally for me, it didn't touch a thing, that should never stop you though, I don't and have never believed in alternative methods and so I'm sure this obviously didn't help. If you can embrace these types of methods they should help. It did cost me money though, if you have the money or access via your NHS for free, go with the free option first before pulling out cash. Again, the internet advises for free, but be careful you don't hurt yourself.
I've had the nerve root injections, again not a thing for me but they often cure, if offered to you, take them, it hurts a bit but isn't that few seconds of pain worth it to get rid of long term agony?
Finally, and the most major, I've had surgery, and yes it cured it - I had three prolapsed discs and foot drop. Surgery should be your last option, and only because of the severity of my condition did I go ahead with it.
Guess what, for a year it worked then one disc popped out the other side and I was back to square one, but do you know what, that's me and my story, we all have one. I'm one case in many and I'm always pleased to hear folks have been cured with whatever treatments they have tried.
You probably couldn't mention much I haven't tried however, what I'm trying to get through to you is that you do what you feel is right for you or possibly what you can afford to do. I understand your pain and how down and frustrated you get but you will find a method that helps. Keep positive and don't let it control you, you are in charge.
Best wishes to you in whatever path you take :0)
nicola2312 nixbadbax
Posted
Tara, how are you getting on?
Nicola
tara95293 nicola2312
Posted
I don't feel that I'm improving much at all. I have 4 year old twins and work 3 days a week which is sitting in an office. I am just getting so so down that I just can't live a normal family life, go shopping, to the park etc.
the consultant said that from the MRI it showed discs 3 & 4 and facet joints 2,3 and 4 all have degenerative disease but it's not bad enough to operate.
Hard to keep my chin up 4 months down the line.