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DX with MS 4 years ago but wasn't told

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    DX with MS 4 years ago but wasn't told

    On February 14, 2007 I had an appointment with Dr. Jeffery, I was referred to him by my primary doctor at the time. I was referred to Dr. Jeffery for the purpose that my doctor suspected that I had MS and Dr. Jeffery was an MS Specialist. My first visit wasn’t that best, he had no bedside manner at all and he did mention that MAYBE there was one spot on my MRI that could possibly be a lesion but it was barely there, so it was hard to tell. He wanted me to have a cervical MRI and come back in six weeks for the results.
    So I had the MRI and went back on April 5. Forgetful me, didn’t take a copy of the MRI with me and he wasn’t happy. He flat out told me to go home and lose weight and I would be fine. So once again I left his office without any type of answers whatsoever and never heard from his office after that.
    As time went on and my pain got worse my doctor referred me to a Rheumatologist to see if they could help me. On my first visit, the Rheumatologist diagnosed me with Ankylosing Spondylitis (AS). Throughout the past few years I have tried every TNF inhibitor to treat the AS, without any luck. Which brings us up to date.
    I was having this weird eye/head thing going on so I went to my primary doctor. He sent me to have and MRI to rule out tumors or any other bad things that might be floating around in my brain. Well the results were multiple lesion consistent with MS. So now I am starting over with a new Neurologist. Since I am going to a Neuro I thought I would contact Baptist Hospital and get a copy of my record from Dr. Jeffery. So when I got the mail, my records were in it. Much to my surprise this is what I read…
    “At this point, I believe we have confirmed a diagnosis of multiple sclerosis. She has additional imaging evidence compatible with that diagnosis by MRI scan. At this point, we will plan to go ahead and start her on Rebif therapy. I will see her back in six weeks. I have talked to her about all the side effects of this therapy. She will return to clinic in six weeks and will check her baseline CBC and liver function test. I wish to monitor interferon and interferon-induced hematologic and hepatic toxicity.”
    Never did he tell me during that visit that I had MS nor did we ever discuss treatment. I don’t know if he got a copy of the MRI later and made the diagnosis and someone forgot to call me, but I NEVER received another phone call from his office again. Bad enough that I was never told about the diagnosis, but now I have been taking TNF inhibitors that has a side effect of demyelinating disease. So for the last four years I could have been treated for MS, but instead I was taking drugs that can cause it as well.

    #2
    My first neuro treated me somewhat the same way. She diagnosed me in August of 2008 without my knowledge. I found out in May of last year. Handy info to know about, huh?
    Rae Roy

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      #3
      This makes me want to request a copy of this last neuros notes. Why, oh why would they do something like that? This blows me away.

      My last neuros notes showed he wrote me off for a nutcase.



      Although, the last visit, the one right before he received the neuro-opths evaluation, he never included in my requested copies. Her evaluation proved his nutcase theory wrong. I'd like to know if it's missing entirely.
      I do not have MS. I have Whatchamacallit; and all of the symptoms are mirages.

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        #4
        I have requested all doctors notes and images. In the first report they had my age wrong and said that I had an LP done, which I never had. It's just crazy!

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          #5
          I recommend always getting copies of your medical records. You'd be surprised what you could learn and it's best to keep an eye out for errors and things like this. You're your own best advocate for health care, and knowledge is power.

          Good luck and hugs,

          Lisa
          Joy is not the absence of suffering. It is the presence of God.
          Cut aspartame from my diet in 2012 and my symptoms have slowly disappeared. Interesting!
          Alpha Lipoic Acid (200 mg) + Acetyl L-carnitine (1,000 mg) = No more fatigue for me!

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            #6
            My neuro and PCP send info back and forth to each other. Sometimes more than I want like when I might be irritated with one of them...LOL Anyway, had my neuro "forgotten" to tell me I had MS (which would have really, really upset me) etc it would have been in the report for my PCP to pick up on. I'm very grateful that they take the time to check up with each other.
            What if trials of this life
            Are Your mercies in disguise?
            "Blessings; Laura Story"

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              #7
              At the very least, you should report him to the medical board for not notifying you of your condition and not treating you. What he did wasn't just a typo on your record. It was much more than that and his peers should be informed.

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                #8
                LOVEJLAWS- SO SORRY THAT HAPPEN TO YOU- IVE BEEN GOING TO JEFFREY FOR OVER 4 YEARS AND I CAN SAY HE WAS OFF WHEN HE WAS AT BAPTIST- NOW HE HAS LEFT BAPTIST AND MUCH BETTER- AS A BETTER OF FACT I TOLD HIM HOW MUCH BETTER HE IS- I MAKE IT POINT TO HAV ALL MY MEDS AND QUESTIONS WRITTEN DOWN AND MAKE SURE HE HAS MY BEST INTEREST AT HEART! AND SO FAR SO GOOD!
                I GOT TO KEEP IT MOVIN-
                ;DM.S. + MY STORY = I WILL SURVIVE THIS STORM TOO! AUDREY R

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