In August, I was (finally) diagnosed with a ruptured L5-S1, central rupture. I had been suffering from horrible back pain and even worse radiculopathy for almost a year. I saw a pain doc on Oct 1, and he did an epidural injection. It took about three days for the injection to work and lasted about another 8 days before it was kaput. The pain doc also put me on Neurontin and naproxen. I called last week, after giving the meds a full two weeks to work, and said that I was still having quite a bit of pain. He upped my Neurontin to where I will eventually be taking two capsules three times a day (300mg capsules, I think) and switched the naproxen to diclofenac twice daily. I don't know which medicine is making me an absolute idiot, but one of them is! What's worse is that they are neither one doing a real good job at managing the pain. I am still working on getting the Neurontin to the full dose he recommended.
I am a teacher and need to be on my toes, and quite honestly, I hate the way I feel. I had better luck with Advil and hydrocodone. Those never made me feel dopey. I go back on November 11, possibly for another injection, but in the meantime, I just wanted to ask...will my body adjust to these medications or am I destined to feel detached, fuzzy, and dull the entire time I take them?
Thanks for any and all advice!!
I'm sorry you're not feeling well. For me, it was Neurontin that made me feel out of it and detached, like I was on autopilot. I hated that feeling and it also tore up my stomach so I could never take more than 200mg a day. Mercifully my doctor switched me to Cymbalta and I find it works better for my nerve pain than Neurontin ever did. I also took Naproxen 500mg which is prescription strength and it made me a little drowsy at times. Of course everyone reacts to meds differently so I can't say for sure if it's one or the other. Personally I would put my money on Neurontin
Maybe your doctor will put you back on Hydrocodone and another nerve pain medicine like Cymbalta, Lyrica, Topamax, etc. Take care
PLS,nerve damage,facet arthropathy,severe DDD,DJD,scar tissue; Fibro
Back Surgeries: Microdiscectomy/ laminectomy,2 level TLIF/Laminectomy w/ hardware, Synchromed infusion pump
Meds: Dilaudid,Oxycodone,Lyrica,Robaxin,Cymbalta,Elavil,Plaquenil
Spineys Rule!
That's rough you're having so much pain. I had some relief after my 2nd epidural and then some(I had 5 total over 20 months). I also found Cymbalta was more effective the same as Meydey. I also took Lyrica similar to Neurontin for a short while after that. I still use my infrared platinum heating pad and it helps while siting especially. Take care and hoe you keep looking for more Neurosurgeon or Orthosurgeon opinions. Charry
Any answers I have is not medical advice only a Doctor can help you with that. Just sharing my personal experience as a fellow Spine Health member only. Mild DDD of complete lumbar area with recent healing of L5-S1 HD and annular tear.Leg &foot weakness nerve compression L4-L5.Mod. disc changes C5-C7 nerve impingement sore elbow and numb hand. Sept. 2011 MRI L4-L5 disc bulge and L5 facet joint and narrowing. Meds-Oxycontin 80mg,Cymbalta,Lyrica, Flexeril,Naproxen,Serax. Platinum Infrared heating pad. ER and Oncology trained and Cardiology RN on Disability. Keep the faith.
I too have problems with Neurotonin and Lyrica. Can not take them at all because of the horride side effects. My brain was in such a fog and could hardly talk let alone walk. I only took one pill but that was enough for me. I could not function at all. It took two days for it to wear off.
I know a lot of people who swear by them. My vision was so blurred I could not call the ambulance
to take me to the ER. I thought it was going to kill me...i really did. Do bot let my experiane scare you. As I said, a lot of people get wonderful relief. I am just one of those people who has ptoblems with meds. The brain fog was just one of the problems I had.
Best of luck to you.
Cheers
Patsy W
I am not a Doctor but I do watch House and Doc Martin on TV.
Never give up HOPE..June 18,2010 I had a pain pump implant....I now free of pain.
My thoughts and opinions are just that, my thoughts and my opinions, based on my experiances.