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    Re: Spinal Cord stimulator

    Posted by Maria on 1/19/09

    I am sorry you had such a bad time with you implant and the
    Doctors. There really are some awful people out there who do
    treat patients like meat. I have been functionally disabled
    since I broke my L5 in 1993, and I also suffered nerve damage
    and spinal cord compression. I am in constant pain.
    I have used a stimulator since 1997 and it changed my life. I
    left it on 24/7. I had the new unit implanted in 2008 and it
    worked well for quite some time, but now I am having more pain
    and have learned of problems with corrosion of the leads, so I
    am now researching this as a possibility of the problems I am
    having.
    As far as your statement that the trial always works, that is
    catogorically NOT true. It sounds like you were poorly treated
    and I feel badly for you, but you do need to make sure your
    statments are true.


    > On 2/18/08, Guy Bodemer wrote: I did not write this:GB
    >> On 2/02/08, Carolina wrote:
    >>> One day in January of 2007 I had an appointment with my
    >>> doctor for injections for lower back pain and pain in my
    >>> legs. I also got prescriptions for medication on these
    >>> visits. I walked to the room I was sent to and there were
    >>> all kinds of different displays advertising Advanced
    >>> Neuromodulation Systems Inc. (ANS) Spinal cord
    >>> stimulators. The doctor then proceeded to tell me how
    >>> wonderful these things were. He said I would be out of
    >>> most of my pain and would have a better quality of life if
    >>> I had the surgery to put it in. He said I would be able
    >>> to travel and visit my grandkids. I trusted this doctor
    >>> more than any doctor ever. I also liked him as a person.
    >>> I believed everything he said. Before I had the surgery
    >>> to implant the spinal cord stimulator he said that he had
    >>> to put a trial stimulator in and that it would have to be
    >>> done in his office. The trial stimulator was done in
    >>> February. The wires were connected to the stimulator
    >>> which was on the outside. I was very excited that it
    >>> worked so well. I found out later that the trial
    >>> stimulator always works and that is why patients get the
    >>> surgery to put the permanent one in thinking it will work
    >>> like the trial one did. An appointment was made by the
    >>> doctor's office for me to go to the doctors office to have
    >>> the permanent one put in. I had never met the doctor who
    >>> put in the permanent one. He was 6 hours late arriving
    >>> for the procedure. Everytime I said I wanted to leave the
    >>> nurse said "wait 15 more minutes he said he will be here"
    >>> He finally showed up and said he worked with my regular
    >>> doctor. Although I was very upset and in a lot of pain, I
    >>> thought because he worked with my doctor and I trusted my
    >>> doctor so much I would go ahead with the surger. What a
    >>> mistake that was. He was rough with me when I cried and
    >>> told him how bad he was hurting me he wouldn't even
    >>> answer. He stapled my back and nobody stopped him. I
    >>> prayed for god to let me die because the pain was so bad.
    >>> All I was to this doctor was money on the table. I
    >>> thought the spinal cord stimulator would work but even if
    >>> i turned it on and walked across the floor it would shock
    >>> me and I would have to turn it off. I could not move or
    >>> do anything with it turned on. The rep from ANS wanted me
    >>> to keep trying to use it. He said I had to keep trying to
    >>> get used to it. He even reprogrammed it but that just
    >>> made it worse. While laying down I turned it on low the
    >>> way he told me to and I injured my legs doing this. My
    >>> legs now shake all the time and tingle. I also have
    >>> trouble with my kidneys since having the surgery. I am in
    >>> the bathroom every 20 minutes. I will have to probably go
    >>> out of state to find a doctor who will even be willing to
    >>> look at it. I had the thing taken out and the pain that
    >>> it caused me is awful. My hip still hurts and thobs all
    >>> the time. I get very little sleep. I went through all of
    >>> this because of greedy doctors and a greedy corporation.
    >>> Nobody explained risks of this thing to me such as loss of
    >>> sensation, loss of limb function, stroke, cardiac arrest
    >>> or permanent damnage to other body organs even death. I
    >>> found this out after I had it removed! Can anyone please
    >>> respond who has had any similar experiences. Fed up with
    >>> doctors in SOUTH CAROLINA

    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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