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Re: medtronic spinal cord stimulator
Posted by Julia Greenborn on 7/12/06
I've had a spinal stimulator in for three years with one revision because my leads got disconnected somehow but have had virtually no problems at all I guess it works for some and not for others from what I'm reading on here so good luck everyone I will be praying you find a happy medium. All the best Julie From Baltimore On 5/31/06, Jackie wrote: > On 5/31/06, Jackie wrote: > Today my pain management and surgeon both want me to consider a scs. As I > have been researching anything I can get my hands on I stumbled upon your > experiences and this concerns me. I have had C5&6 cervial fusion, C2-7 > laminectomy, L5&6 discectomy, L5&SI 1 laminectomy. All my trips under the > knife have not helped the pain from my neck to my toes. I have taken > oxycotin, methadone, perecets, and fentanly patches with a morphine base > drug. ALL have not helped my pain levels. My next step recomended is scs now > I am concerned as I read your side effects and wonder where do I go? I do > know prior to my first surgery c5&6 i have electrical jolts shooting from my > neck down my arms and legs. The more I felt those shocks the more damage I > did to my spinal cord. as my surgeon said I was a cough, a sneeze, a step > away from being a paraplegic according to my surgeon. I am living proof > today that the damage I did has never healed or returned no matter what I > have done to work at regaining my losses. Your doc lied straight out to you! > If you feel that shock with the slightest of movement you are cutting, > piercing, pressing upon the spinal cord and any damage you do it will never > ever repair itself back to the way it was. Even in the healing process you > always leave a scar. I live it everyday. I just read on the morphine pump > some cons also, the side effects are a risks also. When you had the scs > implant did pain management reduce your pain medication? Did the scs ever > work? I am still on the edge looking or help? I hope I have helped you to > understand the losses from the shocks. jackie >> On 5/31/06, Jackie wrote: >>> On 5/20/06, debbie wrote: >>>> On 5/20/06, debbie wrote: >>>>> On 5/15/06, Darek Haupt wrote: >>>>>> On 5/15/06, Darek Haupt wrote: >>>>>>> On 5/08/06, janis wrote: >>>>>>>> On 5/07/06, Michele wrote: >>>>>>>>> On 4/19/06, Janis wrote: >>>>>>>>>> Has any one had this implant turn on with out the remote >>>>>>>>>> and causing stimulation through out the whole body? If so >>>>>>>>>> could you please let me know by e-mailing me. >>>>>>>>> nfler4@msn.com >>>>>>>>> Janis, >>>>>>>>> >>>>>>>>> Yes I only had the scs for about 7 months but two different >>>>>>>>> times in the middle of the night it shocked my whole body >>>>>>>>> and I thought I was going to die I was able to move just >>>>>>>>> enough to grab the remote and shut it off. I thought for >>>>>>>>> sure I at least had nerve damage because it was like being >>>>>>>>> stuck by lighting. O f course I called the doc the next day >>>>>>>>> and he said it was no big deal (like I was being a big baby) >>>>>>>>> and there is no way it can damage you. After all I went >>>>>>>>> through with the scs I very much doubt that is the truth. >>>>>>>>> You can see my post from 5/6/06. I believe he lied and >>>>>>>>> changed his story about the scs all the time and now I need >>>>>>>>> an MRI becasue my spinal surgeon (not the same person) >>>>>>>>> believes that I have spinal cord damage from the wires. I >>>>>>>>> am now wondering if and how I should go about getting a >>>>>>>>> lawyer, Thank god I found this site and I would tell anyone >>>>>>>>> to think it over very carefully before getting one. I am >>>>>>>>> sure it helps some people (not enough to have it on the >>>>>>>>> market) but at what cost, drugs are far more safer in my >>>>>>>>> opinion. >>>>>>>>> >>>>>>>>> >>>>>>>>> Michele >>>>>>>> >>>>>>>> Michele. >>>>>>>> Could you please let me know your permanent nerve damage. Also >>>>>>>> did you have the implant out and do you have the original >>>>>>>> implant that they took out? I'll let you know about the legal >>>>>>>> end. >>>>>>>> Thank you for responding, >>>>>>>> Janis >>>>>>> I had the spinal cord stimulator implanted July 28, 05'. I had >>>>>>> problems with the leads migrating away from my spinal cord and >>>>>>> felt no stimulation. The surgeon went in a second time to correct >>>>>>> the migration suturing the leads into the muscle. I then had a >>>>>>> hematoma grow on my spinal cord and had SEVERE electric >>>>>>> shockwaves going from my neck to my legs everytime I moved my >>>>>>> head the slightest bit. The surgeon said I was close to being a >>>>>>> paraplegic due to the growth but a major steriod treatment in the >>>>>>> hospital for a third time rectified the situation. I continued to >>>>>>> have erratic stimulation. The voltage was increased to widen the >>>>>>> pain relief area but no go. The stimulator now only works on the >>>>>>> left side and only when it wants to. I am having the stimulator >>>>>>> removed this Thursday the 18th and after the healing period, my >>>>>>> pain mgmt. doctor suggested that the next stage for my pain >>>>>>> management in my back is the implantation of a morphine pump. I >>>>>>> need info. from anyone who has had a morphine pump put in to tell >>>>>>> me if the are better or worse.....is it uncomfortable to live >>>>>>> with?....is it as obvious under the skin as the stimulator >>>>>>> was?.....how is the pain relief? I would really appreciate any >>>>>>> reply. Darek....my e-mail is dwhaupt@comcast.net T
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