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Woman sues hospital after she says doctors missed her MS diagnosis

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    Woman sues hospital after she says doctors missed her MS diagnosis


    Woman sues hospital after she says doctors missed her MS diagnosis

    Sara Allison says she has filed a lawsuit against St. Luke's Health System and two neurologists.

    A Missouri woman says her multiple sclerosis diagnosis was a long one that has led to her filing a lawsuit against St. Luke’s Health System and two neurologists.

    “I started seeing a neurologist probably in 2007 for migraine headaches,” Sara Allison said. “But after a couple of years of treatment, she suspected something more was going on.”

    Her newly filed lawsuit describes a cluster of new symptoms that began emerging in 2012.

    The reported symptoms included slower cognitive functioning, changes to vision, difficulties speaking and immense fatigue.

    She said her doctor ordered an MRI and it showed white spots on her brain.

    According to her lawsuit, she directly questioned her doctor whether it could be MS.

    She alleges he dismissed those concerns.

    “He just said, ‘No, Sara. It’s not. There’s no way. It’s a migraine. This is typical for migraine. You don’t need to worry about these white spots,’” Allison said.

    In her lawsuit, Allison argues more sophisticated testing wasn’t done, despite her questioning.

    The filing describes how the years rolled by, into a full decade of recurring neurological problems.

    As Allison pushed back, the lawsuit claims she was eventually told to seek another doctor.

    St. Luke’s Health System released the following statement regarding the situation:

    “Saint Luke’s is deeply committed to providing the highest level of care to every patient. While we are unable to comment on pending litigation, we can say we are proud of the exceptional care we provide and have the utmost confidence in our physicians who dedicate their lives to serving our patients.”

    Eventually, Allison said she went to get a second opinion with another specialist who ordered a battery of tests and made a diagnosis that she indeed have MS.

    Allison believes she has lost a lot of time for treatment — time that could have made a difference in her life.

    “As time went by, you know, you start to chip away at your life,” she said. “There goes my career. There goes traveling, and there goes having kids if you’re going to do that.”

    Allison said her days are now filled with therapy. She works on things like balance and recognition. She plays the piano, but it’s more frustrating than it was years ago. Trying to read the music as she plays has become more difficult.

    “My life completely changed in a 5 to 10-year period,” Allison said.

    She said she is learning to adapt but wonders what life would be like if she had an earlier diagnosis.

    “I want the doctors to understand that there is a very real consequence in my life for how this happened,” Allison said. “There was a series of decisions that were made that I really didn’t have any say in, and yet here I am with the broken pieces of my life, trying to put it all back together.”

    Allison said she wants others to learn from her experience.

    According to medical experts, if you are seeking a second opinion, get all your medical records to share with the new physician. This includes labs and test results. Insurance general won’t pay for duplicated tests.


    https://www.wbrc.com/2023/12/02/woma...-ms-diagnosis/

    #2
    What a shame and not totally unusual that it was thought to be the sequela from migraine as there can be spots on MRI from a variety of things which increases as we get older. Who knows if her course of MS would have been more mild if treated early but unfortunately she didn't have the opportunity to find out. This is unfortunate for all involved and I hope treatment now will slow her progression.
    He is your friend, your partner, your defender, your dog. You are his life, his love, his leader. He will be yours, faithful and true to the last beat of his heart. You owe it to him to be worthy of such devotion.
    Anonymous

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      #3
      Wow! A shame, indeed!

      My story is very similar. When I first had symptoms in a small town in Alaska over 30 years ago, the old (and old school) doctor said it was all in my brain and I was having a nervous breakdown. Then I moved away to the lower 48 in the mid 90's and was told by another doctor that I had lupus. A different doctor said it was anxiety. A third doctor thought it was a stroke!

      Finally, in all, it was many years before I got a definitive dx of MS after an MRI and other tests. What a waste of years! Of course, back 30 yrs ago there weren't any treatments available, but there were treatments when I moved in the mid 90's and all the doctors missed the mark.

      Now I am SPMS and have always thought I'd be better off if I had been accurately dx. Who knows for sure?
      Never even thought to sue any of these doctors.
      I wish her well.
      1st sx '89 Dx '99 w/RRMS - SP since 2010
      Administrator Message Boards/Moderator

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        #4
        Yes it is a shame. I hope she wins the lawsuit. I wish her all the best
        God Bless Us All

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          #5
          It's a shame but not unusual. MS symptoms can be so non-specific..

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