I was wondering if someone could offer me some advice on whether you feel a visit to Mr Knight of the Spine Foundation would be worth the pain and travel? (Although I am only in Leeds)
I had a spinal fusion L4/L5 and may of been L3 too (I can’t remember) I had an accident while doing a sporting event called Zorbing when I was struck in the back by a large bale of hay.
My fusion was in 2006 (I think) carried out by Mr Dunsmuir in Leeds (privately).
I have had no improvement at all and am on Oxycodone 80 mg 2x daily and diazepam for when I get spasms but my gp refuses to supply any more than 14 a month. I have been on gabapentin (a long time ago) and various other drugs including patches, anti inflammatorys, MST and other pain relievers on top of the Oxycodone. I also see Karen Simpson (pain management specialist in Leeds) she has given me different injections including Facet Joint injections, epidurals, and dorsal blocks all which work but only for a short time and my insurance company will only fund 1 per year.
I am now 36 and had my accident in 2003. I do not have a quality of life, I can’t work, I can’t sit, sleep, stand or walk for long and am in continuous pain.
I have recently returned from my holiday and the plane journey once again ended in traumatic pain and am now laid up in bed again. However previously have been ambulanced off the plane which is traumatic for my family to watch.
Once winter arrives I am nonexistent as the cold makes it a whole lot worse and pretty much from end September to March I am laid up in bed.
I am at a point where I feel I can’t continue like this I have a horrible existence and finding the meds I am taking are also causing me horrific stomach pains. I have seen m daughters life pass by and now she is about to go off to uni and I have missed out in a huge chunk of her life. I suffer from depression and my long term partnership with my boyfriend suffers as I get incredibly angry with myself that I don’t live just exist.
I contacted Mr Dunsmuir and he said he doesn’t know of anything else that can be done. I am unsure that because I had the fusion done that my options of anything else to help me is limited if not ended.
Any advise anybody can offer will be greatly received, I spoke with Bupa today but they have to speak with someone else with regards to funding seeing you (I am unsure why this is) but they said they will come back to me soon. I have my last dorsal block done in January but this time it only lasted 6 weeks or so and cannot have any more until January next year according to Bupa policy.
I don't know where else to turn or what else to do I am now of the feeling if noone is unable to help this is going to be my existence for the next 50 years.
I had a spinal fusion L4/L5 and may of been L3 too (I can’t remember) I had an accident while doing a sporting event called Zorbing when I was struck in the back by a large bale of hay.
My fusion was in 2006 (I think) carried out by Mr Dunsmuir in Leeds (privately).
I have had no improvement at all and am on Oxycodone 80 mg 2x daily and diazepam for when I get spasms but my gp refuses to supply any more than 14 a month. I have been on gabapentin (a long time ago) and various other drugs including patches, anti inflammatorys, MST and other pain relievers on top of the Oxycodone. I also see Karen Simpson (pain management specialist in Leeds) she has given me different injections including Facet Joint injections, epidurals, and dorsal blocks all which work but only for a short time and my insurance company will only fund 1 per year.
I am now 36 and had my accident in 2003. I do not have a quality of life, I can’t work, I can’t sit, sleep, stand or walk for long and am in continuous pain.
I have recently returned from my holiday and the plane journey once again ended in traumatic pain and am now laid up in bed again. However previously have been ambulanced off the plane which is traumatic for my family to watch.
Once winter arrives I am nonexistent as the cold makes it a whole lot worse and pretty much from end September to March I am laid up in bed.
I am at a point where I feel I can’t continue like this I have a horrible existence and finding the meds I am taking are also causing me horrific stomach pains. I have seen m daughters life pass by and now she is about to go off to uni and I have missed out in a huge chunk of her life. I suffer from depression and my long term partnership with my boyfriend suffers as I get incredibly angry with myself that I don’t live just exist.
I contacted Mr Dunsmuir and he said he doesn’t know of anything else that can be done. I am unsure that because I had the fusion done that my options of anything else to help me is limited if not ended.
Any advise anybody can offer will be greatly received, I spoke with Bupa today but they have to speak with someone else with regards to funding seeing you (I am unsure why this is) but they said they will come back to me soon. I have my last dorsal block done in January but this time it only lasted 6 weeks or so and cannot have any more until January next year according to Bupa policy.
I don't know where else to turn or what else to do I am now of the feeling if noone is unable to help this is going to be my existence for the next 50 years.