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Buggered up lower back
Hello People,
I am in pain.....I don’t know how I did it but I have stuffed up my lower back, I have seen dr and they say to lose a bit of weight and move around a bit more. Been doing core excerises but it hasn’t done much. I now have a sharp stabbing pains and can’t run or walk fast. I rely one KAFO splints on both Legs and crutches. I now get numb and pins and needles at night and whist sleeping and daytime. I hope I don’t need a wheelchair further down the future!!!!
Been a year since both my legs packed up whist at London in my brother’s house that has a lot of stairs. Regrettably it forced me to give up my beloved train work I used to love so much. Been missing it ever since as I amounted to a proud position of Master Train Roofer and had a nice little fleet of carriages to repair and maintain, ever since I missed it so.
I have prided in my mobility so much and the day I was forced to use crutches I found hard to accept that I had use crutches full time..I would be so disgusted if I had use a wheelchair as I value my two legs and walking with aid two crutches means a lot to me and it’s hurt my pride that I have use crutches, but if I am forced to use a wheelchair I’ll do it at the last option.........But if I have to it’s not do it because I want to, it’s do it or else!!!
Going to get treatment soon. Wish me luck!
A broken down Train Girl
Comments
Hi @SNUFFLES! I'm sorry to hear that you're in so much pain. It sounds like the doctors are being a bit dismissive. It's really awful when chronic pain stops you from doing the things you love and being able to function. While your situation is different to ours, my family has gone through similar experiences and I'd like to share some of the things I've learned along the way.
My sister has to use mobility aids. While it's frustrating that she can no longer walk, sometimes there were a lot of positives of using the aids. We were able to get easier access to rides, unobstructed views of events and special taxis. Staff often went above and beyond to accommodate her and ensure that she could still enjoy holidays and fun outings. I think accessibility is improving overall. I know that for some people it can be really hard to accept though and they don't want to be pitied or receive special benefits.
Another thing that helped us when we had chronic pain was to put our issues in perspective. There was always someone out there who had it worse than us. When my sister was still using crutches after having knee pain and surgery, I used to see cases of complex regional pain syndrome and people who were less mobile and think, 'Thank God she's not like that'. But lo and behold, she ended up getting a severe form of CRPS and functional neurological disorder and is now virtually bedbound. She is now only able to leave the house to attend medical appointments or go to hospital. To go in and out of the bathroom, she has to call on three nurses to hoist her in and out of a commode chair. She needs help going to the bathroom and showering. Even using a wheelchair for long periods of time is painful. While she is an extreme case, there are probably others who have more complex health needs. We are very lucky that she can have treatment and is currently being looked after by a top team. Not many people can have that opportunity.
Similarly, one of our family friends has a severe condition. He is in a lot of pain and needs knee surgery but because of his other condition, he has a higher risk of infection. His wife refuses to agree to him having the surgery because if he gets an infection, there is a small chance of him needing an amputation. But the surgeon said even if he does end up having an amputation, is it really that bad? His mobility will be greatly improved with a prosthetic leg. Right now, it's hard for him to mobilise.
When my family and I were still waiting for a diagnosis for my sister and for her to be seen by specialists, we were told that all it would take was to find a doctor who has seen her condition before and knows what to do. It took months, but I believe we finally found a good psychiatrist who has a special interest in cases like my sister's. She was able to explain her condition really well and what we can expect from treatment. She gave us hope that she would eventually get better. There has to be someone out there who can do the same for you, so don't give up searching. Both of us had a lot of bad experiences from people who treated us badly, misdiagnosed us or didn't know what to do, but we were able to find experienced professionals in the end.
I hope the treatment works out for you and you can get some relief for your pain.
Hello again people
My lower back is still a hassle but I am using painkillers and seeing a Physiotherapist and doing exercise to help my lower back muscles and weak leg muscles......I still have trouble walking a good distance without stabbing pains going through my lower back and hips.It drives me nuts as I used to be able walk any distance I wanted! Give me the s***s does it ever!
I have some good days and I have some rotten bad days....But I am hoping my lower core exercises can help strengthen those weak areas and stop them rotten back spasms as they are slowly ruining my mobility. Had a CT scan on my spine and nothing was found...good news ,as structurally my back is sound. So it all muscular pain and spasms.
I have been using the Exercises to help my mobility to ease the cramping muscles.....hopefully one day I will get my strength back in the lower back again along with my legs.
Those exercise worked.......my lower back no longer hurts me and my exercises worked and I am pain free. getting my fitness back, pills changed and losing some unwanted pounds has made a lot less harder on my joints.
Hey @SNUFFLES just wanted to jump in here and say that I'm so glad to hear that the exercises were helpful for you!
As someone who has used mobility aids in the past (and still walks with a limp) I can imagine how frustrating it would have been for you to be so restricted.
I admire your resilience in pushing through the difficult time, and please know that everyone on the forums is here to listen and support you whenever you need
@SNUFFLES I'm so glad you're feeling better! All that hard work with the exercises must have paid off.
@SNUFFLES ouch... hopefully the treatment helps. Has your doctor referred you to a neurologist or someone similar?
Chronic pain sucks... I have leg and lower back pain for some unknown reason, so I walk with a cane now.
I think I know what you mean about your pride.
It can be especially embarrassing to publicly show that I cannot do something that most people manage without even thinking about it.
The way that I cope with those feelings is to completely own my cane.
I find that if I act like it's something to be ashamed of, I feel worse, so I try to show pride in myself, cane and all. I think it's a way of showing myself that there's nothing to be ashamed of.
So when I'm sitting down, I try not to hide it between my legs like I sometimes want to.
It is bright and sparkly, because if I'm going to have it, it may as well be fun. When people stare at me, I look back at them.
It helped me accept it much easier. I actually think I'm more confident since getting my cane, simply because I had something to show confidence about.
It's also helped me to find role models who also use mobility aids.
I know of a passionate, determined human rights advocate. The fact that they use a walking stick and a wheel chair does not cancel out the amazing work that they have done.
My grandmother lived through her town being bombed in WW2, and grew into a forgiving, empathetic and extremely persistent person, and her using a cane does not change how much I admire her strength and resilience.
When I can look up to someone in a similar situation to mine, it helps me feel more acceptance towards myself.
that's amazing that your grandmother is like that!

