I have had burning/stinging in my legs for 3 years. Then, I had a car accident in 6/05, irritated a previously
herniatedHerniated nucleus pulposus disc at C7. By 11/05 I began experiencing back pain,
rectalAnorectal fistulas
Colon cancer
Colorectal polyps
Digital rectal exam
Hemorrhoids
Imperforate anus
Imperforate anus repair
Inflatable artificial sphincter
Proctitis
Rectal biopsy
Rectal cancer, x-ray pressurePressure ulcer, etc. By Spring of '06, back pain became unbearable. By 12/05, the nerves in my spine began to
stingSting-kill, and I have neuropathy related constipation.
My D.O. ordered an MRI in 1/07, and an EMG 2/07.
MRI:
1. Mild
centralCentral sleep apnea
Central-vite bulging of the disc at L4-5 and L5-S1 with no evidence of
compressionCompression of the median nerve
Cpr - adult
Cpr - child (1 to 8 years old)
Cpr - infant.
2. No bony stenosis is noted.
3. Otherwise MRI of lumbar sine is unremarkable.
EMG:
1. Minimal sensory neuropathy.
2.Questionable mild S1 radiculopathy on the right side, given and absent H-reflex.
My D.O.'s nurse told me I have a compressed nerve and referred me to a Pain Management Doctor.
Can you tell by these results, which nerve is being compressed, and how can Pain Management help me?
You may want to consider Atlas Orthogonal Chiropractic as some people in your situation have found great reflief. Any neurologist worth his weight will tell you that operations are always a last resort. You may also want to look into the DRX9000 which is proctored by doctors of chiropractic, but, is also supported by many neurologists.
Hope this helps. Sorry for all of your pain.
Peace.
I am wondering if the pain management doctor will know how to de-compress the nerve, or if is he just going to "manage" my pain, with medications.
Absolutely. I think that DRX would work for you, but, a general doctor may not agree. You need to simply go and see them. Google it.
JCmcc.
Sorry for getting your name all mixed up, Lyrica has me in another zone. :(
I agree, I think the disc compression would help me. I need to find out if my insurance covers it, because it can be very expensive.
I am curious to find out, what treatments the PMD recommends. I am not committing myself to anything, unless I am convinced he can help me.
I don't want my pain "managed", I want the reason for it, fixed.
When the Dr amputated it I watched it was cool to see your bones. anyhow that is why I know I am in pain. I have had four nreve blocks on the left side of my head in the back that did not help. It gave me a numbing feeling for a few days and then the pain worsened.
The meds I have been on are..... tegretol, indomesion,nerurontin,amitriptelyine, topamax,imitrex,percaset,naproxen,tremedol,skelaxin, now cymbalata. nothing is working. I was denied SS disability because they feel I can do light duty. NOT I am in pain right now just typing this blog. I also get a pressing feeling aroung my skull thats all the way around, like a migriane with needles and burning sensation. I have passed out and I get very light headed and have to lie down. CAN ANYONE HELPME
liza.***@****