After 7 months of unrelenting back pain, I feel as if I am back at square one. I have been on gabapentin and lyrica with no relief, 2 l/5-s/1 injections, a l-5/s-1 and s-1/s-2 injection, and a piriformis injection...all with no relief. Having had no movement in my toes for a little over 3 months my doctor sent me for an emg/nerve conduction study. I had that done on Tuesday and have been stressing about it all week.
He did the test and when he was finished I asked him how it went and he said that my weakness wasn't stemming from my herniated discs and it was most likely something neurological or in my spine. I see my regular pm doctor on Monday to discuss the findings.
The reason I am very concerned is bc about 10 years ago after dealing with crippling migraines I finally saw a neurologist who discovered spots on my brain. I went through all of the ms diagnostic tests and I was negative for ms. They were never able to determine what the spots were from and assumed it was just scarring from my migraines. I am concerned now that it could possibly be ms or some other neurological disorder.
After completing the emg the doctor prescribed me prednisone and gave me instructions on tapering it for 8 days. I am on day 5 now with no change in the ability to move my toes. I had the piriformis injection done 2 weeks ago with no change in my pain. I'm scheduled for a si joint injection in 2 weeks if the doctor decides to do it. The last time I saw him he told me that my amount of pain and weakness is not explained by the size of my herniated discs and therefore he can't figure out where the pain is coming from.
It's been a very frustrating 7 months for me and I just want answers at this point. I was hoping the emg would provide the specific spot of where the weakness is coming from but that now just opened up a new can of worms. I wish this was an easier process with more success on the pain front as nothing I have taken or been prescribed has helped with the pain