I have cervical myelopothy C5/6
On an average day my pain levels never go below 6, when I experience a flair up usually its 8- to 10 , and the flair ups can last for weeks until it subsides,
I’m constantly dropping thing, all glass ware in my house was changed to plastic, I have ceramic floors.. I have no feeling in my hands; I can feel pressure, but no sensation. In other words I can not tell if I’m touching sand paper or concrete, and touching steel is very unpleasent.My right side has been most affected. I can still use my arms and fingers I just got to focus on the task on hand. I learned to compensate, by applying thought and patients relearning tasks that healthy people take for granted.
I will give you a prime example; a typical day , I make my self a mug of hot coffee, I hold it in my right hand (I’m right handed) as long as I’m mentally aware that the mug is in my hands everything appears normal the second the phone rings and my concentration is broken ,another one bites the dust,
I find it amazing how the human body can adapt to changes. I had to re learn just about everything, I always must be aware of my present surroundings. My physical situation does not compare, pain wise, to my skin sensation with out medication.
I can describe this as the most debilitating for me, This is the reason I have such trouble describing my pain to some one:
My neck/head/shoulder blade area –burning, itchy pins and needles, always stiff and a dole soreness but constant. most of the time not bad enough to incapacitate me but bad enough to drive me nuts, then there is my right fore arms, in a flair up situation I’m convinced its going to explode just below the elbow, this pain usually radiates to my fingers which are constantly stiff and pain full but still usable.
Then there are my legs. Extreme itchy, burning, ants crawling, those pesky shooting pains which usually hit with out warning; sharp stabbing pains in my ankles and feet mostly. This lasts maybe a few seconds, boy do they hurt. My legs are wobbly , they work but not like most peoples, once again I have to focus on my stride. When I walk my right leg has a tendency to drag. Two winters ago I was walking on ice and some one blow there car horn behind me before I new it I was in the hospital with a spiral a tibia fracture.
And for the icing on the cake these nasty muscle spasms
My neurologist tells me that most of the sensations I’m experiencing is caused by the myelopothy sending wrong signals to the brain,
I still love life
A little back ground;
I’m a 48yrs old male, I have moderate to severe chronic pain everyday of my life for the past10 years,
I was diagnosed with, sever stinosis in the neck, severe D.D.D ,
At 37 I had to have a lamanectomy from C3 to C7 inclusive, do to herniated disc, and myelopathy affecting my spinal cord. The doctors have made it very clear ; there is real nothing left to try, medically. Also the same goes for the pain situation aswell.Which means this is it…..
Presently I can not feel with my hands, no sensation, I have pain from my head to my toes. I have been on every type of pain medication and all stopped working after a while
Now I take Lyrica and and medical marijuana
(My advice to the world ,” acceptance, never give up, keep your self occupied . get physiological help, just to put things into prospective. Try to smile)
Have you investigated Myofacial Pain Syndrome.
I also have neuropathy in my arms and hands from DDD.
Also have had laminectomy and a fusion.
Was unable to function well at all and no work until
I was diagnosed with MFS
I now have stretches etc and see an Osteopath biweekly.
I am able to work! ! It is painful but I do it.
I also take Neurontin and it helps the heavy tingle,pain
and numbness in arms and hands.
Please look into MFP and try to find a Doctor of Osteopathy.
Called Dr in US but only Osteopaths in Canada.
I am taking 3000mg of Gabapentin a day.
Any less and the neuropathy comes back too strong.
We are all so different and react differently to meds.
LOL Yes I am awake.
I started lower and went up to 3300mg, then tried to switch to something else and that was a "horror" so much pain! ! !
Then went back up to 3000mg. Have tried to go down 100 at a time, but can't get very far down so I will stay where I am.
Not only awake but putting needles into people at work (I work in a medical lab) LOL, honestly.
Could not be working without Gabapentin and stretches for mfp.
Post Edited (lois22lane) : 11/9/2008 2:16:59 PM (GMT-7)
JJ how is it going?? You have not replied to us.
Please let us know.