Anyone tried Spinal Cord Stimulation for Chronic Pain?
Spinal Cord Stimulation – A Compelling Treatment Alternative for Chronic Pain https://www.hss.edu/conditions_spinal-cord-stimulation-treatment-alternative-chronic-pain.asp
Vladimir N. Kramskiy, MD Assistant Attending Neurologist, Hospital for Special Surgery, Clinical Assistant Professor of Anesthesiology, Weill Cornell Medical College
What Is Spinal Cord Stimulation?
Read more here: https://www.hss.edu/conditions_spinal-cord-stimulation-treatment-alternative-chronic-pain.asp
Posted: 10/8/2018
Anyone tried Spinal Cord Stimulation for Chronic Pain?
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What other options do you know about? Would like to know. Thanks
What time of the day do you take the Tramadol and pregabalin. Morning or bedtime? I take 50 mg of pregabalin at bedtime and wanted to know your schedule
Which brand? So you never had it in ur legs?
Hi Betty,
I take 50 mg of Pregabalin with 50 mg of Tramadol every morning about 8 a.m., and both again in the afternoon at about 3:30 - 4:00, and then again at night at about 11:30. I also take 0.5 mg of Ropinirole at 11:30 for restless leg syndrome. I'm a night-owl so I'm always up past midnight. My foot pain had kept me awake for many years but this regimen works well for me. Hand pain, which I never used to have, is often very bad in the morning until those 8:00 pills kick in, and then it is well controlled during the daytime.
Hi Betty,
I have a PT appointment every week, and as part of the therapy, I get deep-tissue laser treatments in both my hands and feet. If the laser isn't designed for deep-tissue, it doesn't work for me. If I go more than a week between treatments, the numbness in my feet is terrible even if pain doesn't increase, and so the chance of falling is greater.
Do you use any other devices such as TENS or at home heated foot baths with massage? Do you have any side effects with the pregabalin? My doctor has recommended this drug but after reading the common side effects I’m a little concerned as I already have most of them and don’t want to make it worse.
I am considering this option because I have severe pain in my lower back and some in my legs and feet. Would you recommend this to others and would you do it again if you had to? I am not one that takes drugs as I am afraid of the side effects.
What company manufactured the SCS device? How long ago did you have the permanent one implanted? I'm happy you got relief. Thanks
I have an Abbott nerve root stimulator implanted Feb 20th. On 3rd program. Seems to dramatically decrease low level pain from 5 to 1 but I still have intermittent spikes like lightning bolts. They are less frequent and not as sharp, also shorter in duration. Still taking Gabapentin 600mg tid and use med Marijuana at night. I'm a bk Amp for 6 years. My good foot is almost completely numb now.
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