Ok - I am going to put this here because it is the thing that is causing me the most trouble atm.
To explain - I have had ME/CFS for 10 years - I had it very severly - bedridden for 2 years in a dark room (dizzy, unable to sleep, no light, no sound, pain, migraine etc etc) - I got a bit better and slipped a disc picking up a piece of tissue. The pain for the next 2 years was excruciating - the whole right side of my body was in almost constant spasm and the sciatic pain was unbelievable. I couldn't move and ended up with bed sores - it was so painfulI couldn't speak or cry a lot of the time - I was having to pee in a bowl next to the bed. I took an overdose and woke up sometime the next day partially paralysed. A piece of my disc had broken off and was pressing on my spine. I had surgery.I was hopeful that would be the end of it. A week after coming out of hospital something in the middle of my back went clunk (there is some loss of height in the disc there) - immediately all of the muscles in my upper back, shoulders and neck went tight - it feels like tortion - like my body is being crushed and pulled in several different directions at once. Everything grates and clunks - my head feels like it is in a vice. Sometimes it hurts to breathe. I have tried massage, osteo, chiro, shiatsu, accupuncture - I was refered to the Input pain programme at St. Thomases but wasn't well enough to get to London and back weekly. I have been like this for 5 years now. I am hoping to do a local pain management programme that starts in April next year.
The problem is I have NO money for any treatments - I have maxed out my credit cards and I live on incapacity and housing benefit. I would like to know if anyone can recommend anything I can do at home that might help. I have tried stretches and core strengthening - With the stretching it helps while I am doing it but as soon as I sit up or move everything locks up again and nothing ever feels properly stretched. I did yoga before I got ill so I know what it feels like to become more flexible over time - this no longer happens - there is no improvement in my in the feelings of crushing and pulling and the vice like feeling around my head. Also even pulling my naval in and up slightly causes all of my other muscles to lock in - I have tried to distract this reaction by, for instance, blowing raspberries and shaking my arms as I do it - no luck. I do Alexander Technique relaxation and some meditation but as I'm sure you can imagine I am really quite stressed out and depressed about my situation. I have also lost my relationship and my home to all of this. I feel like I am lost. I feel ill everyday - sometimes I can't even get to the doctor to get my prescription.
Currently the only thing that helps at all and allows me to be able to sit up at all for more than 20 minutesis Diazepam.
I also have Essential Thrombocythemia which is a bone marrow problem that causes my stem cells to make too many (and abnormal) platlets - I just take asprin for this atm although if it gets worse I might have to take some chemo tablets.
ANY advice on where on earth I could start in an attempt to unravel all of this would be really appreciated.
I am going to put this in the pain and fatigue forum as well - I hope that is OK(?)
Good thoughts to all,
Joss
To explain - I have had ME/CFS for 10 years - I had it very severly - bedridden for 2 years in a dark room (dizzy, unable to sleep, no light, no sound, pain, migraine etc etc) - I got a bit better and slipped a disc picking up a piece of tissue. The pain for the next 2 years was excruciating - the whole right side of my body was in almost constant spasm and the sciatic pain was unbelievable. I couldn't move and ended up with bed sores - it was so painfulI couldn't speak or cry a lot of the time - I was having to pee in a bowl next to the bed. I took an overdose and woke up sometime the next day partially paralysed. A piece of my disc had broken off and was pressing on my spine. I had surgery.I was hopeful that would be the end of it. A week after coming out of hospital something in the middle of my back went clunk (there is some loss of height in the disc there) - immediately all of the muscles in my upper back, shoulders and neck went tight - it feels like tortion - like my body is being crushed and pulled in several different directions at once. Everything grates and clunks - my head feels like it is in a vice. Sometimes it hurts to breathe. I have tried massage, osteo, chiro, shiatsu, accupuncture - I was refered to the Input pain programme at St. Thomases but wasn't well enough to get to London and back weekly. I have been like this for 5 years now. I am hoping to do a local pain management programme that starts in April next year.
The problem is I have NO money for any treatments - I have maxed out my credit cards and I live on incapacity and housing benefit. I would like to know if anyone can recommend anything I can do at home that might help. I have tried stretches and core strengthening - With the stretching it helps while I am doing it but as soon as I sit up or move everything locks up again and nothing ever feels properly stretched. I did yoga before I got ill so I know what it feels like to become more flexible over time - this no longer happens - there is no improvement in my in the feelings of crushing and pulling and the vice like feeling around my head. Also even pulling my naval in and up slightly causes all of my other muscles to lock in - I have tried to distract this reaction by, for instance, blowing raspberries and shaking my arms as I do it - no luck. I do Alexander Technique relaxation and some meditation but as I'm sure you can imagine I am really quite stressed out and depressed about my situation. I have also lost my relationship and my home to all of this. I feel like I am lost. I feel ill everyday - sometimes I can't even get to the doctor to get my prescription.
Currently the only thing that helps at all and allows me to be able to sit up at all for more than 20 minutesis Diazepam.
I also have Essential Thrombocythemia which is a bone marrow problem that causes my stem cells to make too many (and abnormal) platlets - I just take asprin for this atm although if it gets worse I might have to take some chemo tablets.
ANY advice on where on earth I could start in an attempt to unravel all of this would be really appreciated.
I am going to put this in the pain and fatigue forum as well - I hope that is OK(?)
Good thoughts to all,
Joss