Peripheral nerve stimulators
This is a long shot, but I’m looking for people who have used implanted peripheral nerve stimulators (PNS) to control nerve pain. They block the pain signal to the brain. Stimrouter and Stimwave are major brands. These are NOT the same thing as spinal cord stimulators, of which there are many brands. I’m about to have a Stimwave implanted to block intractable pelvic and leg nerve pain.
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@sunnyflower @sprinrosa64 The doctor that did my DRG implant is a Pain Doctor and Anesthesiologist. It is very common in Illinois that pain doctors do these implant procedures. I never even thought to ask for a neurosurgeon to implant my device. I didn't think to ask many important questions, and sadly trusted just my pain doc as to the device. Too late, smart.
@faithwalker Renee, My goodness, girl; thanks for all you write about these stimulators, and for clarifying info about the leads. You clarify information very well, and I so appreciate that. I cannot imagine doing a pain stimulator without a psych evaluation, as the whole experience is grueling. It is not for an unstable, very nervous, clinically depressed person to handle. My pain doc did explain why the psych eval was so essential, and I did appreciate that. I have gone through Hell with this device, and I know that a state of clinical depression would have made it that much worse. Thanks a bunch! LoriRenee1
@faithwalker Hi Renee, Could you tell me what "Shock" and "Continuous" even mean in terms of the DRG stimulator? God, I do not know much about my programming. I only know that I have been given 4 programs since my implant in July. I go to my Pain Doc, and the ABBOTT rep is there at the same time. The ABBOTT guy generally adjusts one lead at a time to a point where I no longer feel electric impulses, and then tends to lower it down more, at least 2 notches. I then go home and see how it feels, and find myself lowering and lowering the electricity, one notch at a time. I live with my adjustment a few days, and within the last month, could not seem to get rid of electric sensations in my butt cheeks and shins, primarily. It got to a point that I could not sit down, and shut it off completely. The whole experience has been grueling, but I too, have about 20-30% pain relief, for sure. So far, with the machine off, the pain relief continues. It just got to a point that I could not tolerate the electric sensations. Fun, fun. I would not wish this on my worst enemy, of which I have none. Thanks again, Renee. LoriRenee1
Absolutely! My pain specialist would not let any other surgeon or provider do it! If anyone ANYONE else attempts to schedule surgery TO YOUR SPINE and they are NOT a neurosurgeon, report them to the AMA!
@lorirenee1 @sunnyflower @spinrosa64 @faithwalker007 At Mayo Clinic SCS trials and implants are handled by specially trained doctors in the Department of Pain Medicine, not by neurosurgeons. Perhaps in smaller hospitals neurosurgeons perform the procedure.
Nice! I will pray for a successful implant and treatment. You sound hopeful and should be.
I did a LOT of research before even embarking on the the trial of the DRG SCS. After being emerged in healthcare for 20 years at that point, I knew and still do, how to read and understand studies.
You are not to blame. At least you had a specialist. I’m afraid many are succumbing to pcp attempting this procedure due to the crackdown on Opioids. The equipment should not be accessible to any other surgeons except neurosurgeons or back surgeons. IMO
I only want people to know what I made myself know through RESEARCH. Lol
My CRPS pain is compounded by migraines, osteoarthritis, IBD, and other fun stuff including secondary depression that a SCS will not miraculously FIX.
I’m sure I’m not the only person with neurological pain with these issues and a SCS is not the cure all for our troubles nor should it be expected to be.
However, it is being promoted that way in many cases. “Oh you don’t need to take opioids, I have an alternative for you.” Its been said to me three times since I’ve had it implanted BEFORE these pain specialists bother to read my chart and when they become aware I have the DRG implanted and it is only carrying 15% (max) of my pain load, they say goodbye.
This therapy is NOT an cure for government’s Opioid dilemma. It is simply another treatment for intractable peripheral nerve pain which is not responding to any other therapy.
“Shock” programming (my term) is the program you can FEEL after he is finished programming it. If you adjust it upwards or downwards, it is programmed to treat your pain with sensation of electrical impulses similar to a TENS UNIT.
“Continuous” (DRG term) programming is NOT EVER supposed to be felt after he is finished programming. If you increase the setting, you STOP and decrease of you FEEL electrical impulses Anywhere.
How are you sitting, or laying when you are being programmed? Stand when he is programming you if you move about at home. Lay flat if you lie down a lot at home.
Your position when he programs affects the intensity of the settings of every program he is formulating in your system.
Tell your rep that you do not understand the programming options. Tell him what is happening at home and that the programs are too intense and you think your body position is affecting it when he programs your system.
Ask him to TEACH you how to use your control system better so you can understand how to adjust your Stimulator and not merely shut it off.
Do you still have any inflammation in your back?