Spinal Cord Stimulator Problems
Posted , 47 users are following.
I have had my spinal cord stimulator since May and I am having a lot of nausea. I have to keep soda crackers with me all the time. The SCS was put in after I had ongoing pain after my spinal fusion. I had an injury from an auto accident. I have had issues with the settings put on the control box by the rep as well. I had to push for setting changes to alleviate sharp shock like symptoms as it was stimulating. There is poor follow up by the reps after the SCS are put in. It seems their goal is to sell the stimulators but the patient is forgotten when it comes to legitimate reportable symptoms and follow up care.
4 likes, 221 replies
marie04822 TreasureNurse
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I agree about follow up care. I've had myStimulator in for about 2 months and the Nevro Rep just keeps adjusting it. I feel like an experiment.
dianneg marie04822
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marie04822 dianneg
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The Nevro Rep down played the surgery. He was wrong. It was surgery to implant the Stimulator. They do a test where they just tape the wires to see if the Stimulator will be effective for you. The test decreased my pain by 50-70%. When they placed the permanent one in place it didn't do the same. Hence, the adjusting. I'm still hopeful.
TreasureNurse dianneg
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TreasureNurse marie04822
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It has taken 5 months to get a good adjustment on my stimulator. I felt played down as well while the rep was commenting on my questions. He did not want to admit I needed an adjustment. But after the adjustment the pain was decreased. They act like patients dont know anything ao they try ro tell you an answer that is not right. I let him know right then and there what I was feeling and that it was not a "mind issue" like he was trying to insinuate. My stimulator had not been set right and he was trying to avoid responsibility.
bonnie_66734 marie04822
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Yttiks marie04822
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tom27472 TreasureNurse
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I am on my second stimulator. No contact from rep at all
First one they took out after three weeks. Had to wait about five weeks to heal. They just did another implant. Same thing is happening when they removed the first one. A lot of pain, can't even turn on know until I heal because they are concerned if will cause infection because battery heats up when on only he 1 degree enough to bread bacteria. So they put the second one last week they admittted me to hospital for 5 days to The debreed the surgical area around the battery. In a lot of pain still draining, unit still not on. Trying to get the truth.
marie04822 tom27472
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DJ1976 tom27472
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bonnie_66734 tom27472
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I can'think handle the thought of going through an implant again to but I am sure the battery is making me feel overheated.
DJ1976 TreasureNurse
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They probably have your stimulator set for tonic which is a constant flow of a tingling sensation and pulsating throughout your leg and back. There is also a Burst setting which incorporates the two where youfeel no sensation. I do not know what stimulator you have. Let me know. I did the NERVO TRIAL with no relief. I just completed BURST by St. Judes Hospital. It is a full 7 day trial. I was reprogrammed after 5 days and on day 6 I got my first relief. We recorded the settings and it is in my nice little apple I phone for when I get it put in permanently.. shouled be hearing from the Surgeon for my first consult and then a surgical date. I must admit I am more nervous as the modulator will be implanted under the skin. They just need to know which side you want it on. Being a right side sleeper I opted for the left side just near the top the the butt. The reps for both the trials I was in have been remarkable and have gone above and beyone even coming to my home for over an hour and reprogramming it. Don't give up. Be firm with your pain management Dr. I didn't have to be she was and is always one step ahead of me. Keep me posted.
socksmom TreasureNurse
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bonnie_66734 socksmom
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tom27472 TreasureNurse
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marie04822 tom27472
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