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.