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    Re: Spinal Cord stimulator

    Posted by Lyra on 3/10/08

    Hi. I just wanted to let you know that I have had a good
    experience with an implanted neurostimulator. I crushed two
    nerves in my left foot on September 5, 2005. I went from
    doctor to doctor while they tried to figure out what I had.
    I was diagnosed with Chronic Regional Pain Syndrome in April
    of 2006 and told there was no cure, only measures to help
    deal with the pain. I was also told that this disease can
    spread, which it has. I went through months of horrible
    sympathetic nerve blocks in my back which I was allergic to.
    All through this time, I was trying to go to school to
    become a Medical Assistant. I found out a week before
    graduation, in May, that I was Permenantly disabled at the
    ripe old age of 32! I got transfered to a wonderful pain
    doctor in Wausau Wisconsin who helped me out. I had the
    trial done in June with wonderful results! I had the full
    implant done on July 31, 2006! It was the best thing because
    it worked just as good as the trial.

    In December of 2007, I had one of my two leads slip. This
    was due to me moving wrong and I broke an anchor. I went
    back to my doctor and just had a lead revision on February
    27, 2008. Without my neurostimulator, I would be crippled
    and confined to a wheelchair by the age of 42. This was not
    something I want to happen! I have three kids age 16, 13,
    and 9. I can't be confined to a wheelchair!

    I don't know how much experience your Physicians had with
    implanting these things, or how much research you did before
    deciding to get one. I did a lot of research before getting
    it because of all the risks involved. I have some problems
    with mine. I can't fully empty my bladder with my stimulator
    on, I do have some pain where the wires and battery pack
    are, and I do get dizzy sometimes when I turn it off. I tell
    you what though....I would rather deal with all that than be
    depressed not being able to do anything because of the
    severe pain I am in without it.

    I am very sorry that all of you have had negative
    experiences with spinal cord stimulators. It sucks to hurt,
    trust me, I know! I just wanted to let you know that there
    are positive experiences too. If you want to ask me any
    questions, feel free. My doctor even has patients who are
    thinking about getting this call me first since I was his
    first patient to get this thing!

    Posts on this thread, including this one
  • Spinal Cord stimulator, 2/02/08, by Carolina.
  • Re: Spinal Cord stimulator, 2/18/08, by Guy Bodemer.
  • Re: Spinal Cord stimulator, 2/18/08, by Guy Bodemer.
  • Re: Spinal Cord stimulator, 2/18/08, by Deb Brinker.
  • Re: Spinal Cord stimulator, 2/23/08, by barbara.
  • Re: Spinal Cord stimulator, 3/05/08, by Andie Pauly.
  • Re: Spinal Cord stimulator, 3/10/08, by Lyra.
  • Re: Spinal Cord stimulator, 1/07/09, by Guy Bodemer.
  • Re: Spinal Cord stimulator, 1/07/09, by Guy Bodemer.
  • Re: Spinal Cord stimulator, 1/14/09, by robert.
  • Re: Spinal Cord stimulator, 1/19/09, by Maria.
  • Re: Spinal Cord stimulator, 2/05/09, by vicki.


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