Mayo Clinic Connect
Has anyone every experienced muscle and facia pain from gabapentin?
Liked by Mamacita, Alumna Mentor
Thank you Lauriedr. I found that treatment so painful with no good results. They injected nine shots in one leg. And nothing. The Dr. told me that it would relax the knotted muscle.
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Hello Gail, thank you for doing some research. In regards to ketamine, or any drug for that matter, this just emphasizes the importance of always working with your medical provider for dosages, use ,and stoppage of any medications. Unfortunately, we are not always able to choose what medications we use, regardless of their side-effects. It is important to do exactly what you did, educate yourself so that you have educated questions for your medical providers. Always work closely with them to address your concerns, and always keep them in the loop regarding starting or stopping medications.
Hello, everyone, I’m new here, & this is my first post. Was I supposed to start a new post, or reply to one? I think this is a reply. I’m Susan, username @sistergoldenhair.
I take Gabapentin, 900 mg/day, (300 mg x3/day FOR Myofascial Pain. Myofascial Pain was described to me as nerve pain. This is how It was explained to me: The Fascia is part of the muscle; the Fascia sometimes ‘binds’ up the muscle, & the nerves in the muscle & Fascia cause the pain. Is this close to being accurate?
This started 14 mos. ago, & came seemingly out of nowhere. Gabapentin helped initially, but not anymore. My doctor suggested a higher dosage, but I don’t want to do that, for the reasons described by some of you in this forum. With this dosage, (900 mg/day), I don’t experience the ‘zombie effect’, or the all over restlessness. Restless Legs is bad enough, AND the Gabapentin doesn’t seem to aggravate my restless legs. According to literature I’ve read, it’s sometimes prescribed FOR Restless Legs Syndrome. I also take Tramadol, which works well for my long-standing low back pain, but has no effect on this Myofascial pain.
Back to Myofascial Pain Syndrome: I take physical therapy; the therapist has minimal training in Myofascial Release, & spends little time with me. I also had several sessions with a massage therapist with extensive training in Myofascial Release. It helped, sort of. Between sessions, the pain returned, and at $125/visit not covered by medical insurance, I couldn’t afford to continue the sessions. Have any of you had Myofascial Release therapy?
I’m back to square one. The pain comes on with exertion, only affects a specific area, the Latissimus Dorsi (sp?), R side of my back. Wen I use that muscle, like reaching for or lifting something, e.g cooking, laundry, cleaning, the pain starts. Continuing to use the muscle aggravates it enough that I have to lie down, & the pain usually eases up after about 20-30 minutes. When I’ve got a crowd of people waiting for dinner, I don’t have time for rest breaks.
This is lengthy because I wanted to let you all know what’s going on, & what I’ve done for it. BTW, It took months of complaining before my Primary Physician referred me to a specialist. It was initially mis-diagnosed by a Rheumatologist as Shingles Neuropathy without rash, & re-diagnosed by a Neurologist as Myofascial Pain Syndrome. Thanks for reading, & I hope you’ll respond with your thoughts or recommendations.
Myofasial Release does work to release the fibers that are”stuck”. My massage therapist has Myofasial release training and can work out most of the Myofasial pain. You can also look at the training videos on you tube and teach your significant other to release many of these fiber knots at home as they appear.
I have found that massage therapist that can do Myofasial Release works for me better than gabapentin. I know it can work for other people but I’m not one of them. I’m the same way with Lyrica.
I have been taking gabapetin for pain in my feet. I have to take a fairly high dosage (1200). I have developed pain in my muscles. I’m beginning to think the gabapetin is causing pain in my calves and other muscles. I really need something for the neuropathy. I took Lyrica and it was great at first but stopped working after a couple of months. I feel like I can’t win for losing. I take one thing for pain and it causes pain somewhere else.
I have the same problem with the pain in my lower legs. I had this with both gabapentin and Lyrica.
I was taking 100mg lyrica, 3 times daily, plus 800 mg Ibuprophen, twice daily, but my new neurologist didn’t think taking the Ibuprophen as a good idea, caused rebound migraines, so he raised the Lyrica to 150mg, and encouraged me to stop the Ibuprophen. He also started me on Propranolol, to help with the migraines. I’ve only been taking it a couple of days, so don’t know yet if it is going to help. I stopped the Botox injections, they weren’t helping the headaches.
Have lower leg and foot pain but I didn’t associate with the gabapentin. Should maybe taper and stop to find out?
First time posting.
I have Chronic Pain over my whole body due to Chronic Lyme disease, bilateral peripheral neuropathy, blood clots, etc.
The point is that I too felt totally out of it with loss of memory, “goofy” or stupid, etc. when first put on Gabapentin. Then my doctor switched me to Gralise which is the extended release Gabapentin.
I still have some memory loss or slowness, but I had that developing before I got on any of the drugs, I take 3x600mg a day (in the evening) which has relieved most of the side effects I got from Gabapentin and I feel it really helps me.
That being said, I think your goal should always be to reduce the amount of medications you take, and I am trying slowly.
I now have 2 pain stimulators (electronic pain blocker). One focusing on the pain from my waistline down and a DRG (Dorsal Root Ganglion) stimulator that is specifically working on my feet. Although it took 3 surgeons and 6 surgeries, the original pain stimulator now works along with the DRG stmulator (only needed one surgery) using “burst technology”. I have had a lot of trouble getting them to get the units adjusted correctly and keeping it there, but when they both are working it takes my daily pain (at least from the waist down) from 7-8 down to 4-5 which is a huge difference in my life. Although I still cannot work, I am hopeful that someday I will be able to hold a job again.
I too have some questions about Gabapentin. I have been taking it for the after affects pf shingles 4 years ago.. The last month I have been having severe feet and leg cramps mostly at night. Could the Gabapentin be causing this? I also have chronic pain because of back problems. I have been told there is nothing that can be done. One July 17, 2017 I had the first of Medial Branch Nerve Block and will have the next on August 18. It has helped about 70% and I am hoping the next will help more. I also have restless leg syndrome.
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I don’t know anything about gabapentin–except that our veterinarian has prescribed it for several of our animals! It seems to help them with pain issues immensely. Other than that, I know zilch. I, too, have restless leg syndrome. I’m not doing anything for it because it’s not too annoying or troublesome.
I tried one time to stop the gabapentin but the needle affect of the shingle pain came back. My husband use to say “getting old is not for sissies”!
I keep thinking that I’m in my 30s or 40s, so I’m always amazed to realize that nope, I’m 64. (Yes, my husband keeps singing the Beatles’ “When I’m Sixty-Four” to me. Off key, yet!) I’ve heard that shingles pain is excruciating. I’ve had the vaccine, but I realize that I can still get shingles. Still, with the vaccine, I hope that, if I ever do get shingles, the pain will be lessened some.
Yes the pain of shingles is terrible. I was in the hospital for 5 days. Mine didn’t break out. My grandson had then after he can home from Afghanistan while serving with the Marines. He he had them on his forehead. He said he felt like Mike Tyson had belted him. Gabapentin does help. I just don’t know all the side effects.
No.I checked the Mayo Clinic and they mentioned other pain relievers as well as the Shingles vaccine.
Thanks for checking for me. Last night I was up walking leg cramps 4 times. I will try taking potassium and see if that works.
A couple of things that helped me with leg cramps at night was sipping a bottle of Schwepps (without the gin) tonic. It has minimal amounts of quinine. As you’re probably already aware, you need to be sure you’re getting enough water. I keep some by my bedside and while it triggers a trip or two during the night to the bathroom – not having leg cramps is worth it. Also triggering leg cramps for me is the unconscious stretching – it’s almost out of my control – the stretching, I mean.
I recall a doctor telling me once that one cause of leg cramps could be a low oxygen level, so I should do deep breathing. I tend to be a shallow breather.
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