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Hello everyone, I am new. Please tell me if this sounds like MS

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    Hello everyone, I am new. Please tell me if this sounds like MS

    My doctor tells me I don’t know after seeing high b 12 levels, blood in my urine.
    High Protein in my urine, high protein in my blood, both my sympathetic and parasympathetic are showing nerve damage. I am getting inside tremors as well as tremors in my hand and feet which nobody sees. My mri scan shows no results while I am having issue with my gait and freezing gait. Blurry vision, chest pain, back pain, numbness, tingling and inside fever without high temperatures. Heat intolerance, excessive sweating anytime, and increase urinating. Constipation, flatulence, diarrhea, tittinus, and feeling like about to fall a sleep during the day, Having a hard time falling asleep, dizziness and balance problems.

    #2
    Hello Mystery101 and welcome to MSWorld.

    Please tell me if this sounds like MS
    Unfortunately, there is no way to know if you have MS simply due to symptoms. There are many conditions, vitamin/mineral deficiencies, some medications, and mental health issues that mimic the symptoms of MS...no symptom is exclusive to this disease.

    Blood tests and urine tests are to diagnose other conditions. There is no blood/urine test that indicates Multiple Sclerosis.

    Your B-12 deficiency should be treated as this can cause symptoms similar to MS. Chest pain should be evaluated by a Cardiologist. Your blurry vision should be evaluated by an Ophthalmologist.

    inside fever without high temperatures. Heat intolerance, excessive sweating anytime,
    If you are a female you might make an appointment with your gyn to check your hormone levels.
    Diagnosed 1984
    “Lightworkers aren’t here to avoid the darkness…they are here to transform the darkness through the illuminating power of love.” Muses from a mystic

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      #3
      Thank you but unfortunately my doctors is just I don’t know. My MRI scans are clear and my b12 is high for no reason.

      Originally posted by SNOOPY View Post
      Hello Mystery101 and welcome to MSWorld.



      Unfortunately, there is no way to know if you have MS simply due to symptoms. There are many conditions, vitamin/mineral deficiencies, some medications, and mental health issues that mimic the symptoms of MS...no symptom is exclusive to this disease.

      Blood tests and urine tests are to diagnose other conditions. There is no blood/urine test that indicates Multiple Sclerosis.

      Your B-12 deficiency should be treated as this can cause symptoms similar to MS. Chest pain should be evaluated by a Cardiologist. Your blurry vision should be evaluated by an Ophthalmologist.



      If you are a female you might make an appointment with your gyn to check your hormone levels.

      Comment


        #4
        We get a lot of questions from people like yourself looking to help us diagnose you without being qualified ourselves.

        What this site can help you with is navigating through the procedures and dealing with stubborn providers. There is no rush to get a diagnosis unless your legs collapse under you.

        But, while you are moving towards a dx, might as well take it slow. Go to the Limbo Landers section of the site. You will find a lot of company and probably get better advice than we can give you.

        Look at it this way. You don’t have MS...YET. Enjoy every moment because the day the hammer
        bangs out the verdict, there is no turning back.

        Comment


          #5
          Welcome to MS World. I am sorry for your symptoms, your current health challenges and your need to seek answers. I wish I could wave a magic wand and it could go away.

          Regarding your question (Does it sound like MS), my neuro often said, "There are lots of other illnesses that mimic MS." Those illnesses will need to first be ruled out, and you will also need to meet the criteria for an MS diagnosis before you can be diagnosed.

          Yes; MS can be a mystery and a puzzle. It took almost 2 years for me to get diagnosed. For some, the path is shorter. For others, it's longer. Because my symptoms were serious and horrific, I even went to Mayo Clinic in Rochester for 2 weeks and had many, many tests and many specialists look at me. They, also, could not diagnose me. They didn't rule out MS, but gave me a different "probable" diagnosis. I had multiple flares, ER visits and hospitalizations during those first years. In addition to lots of other tests (both locally and at Mayo), I had 7 MRI's prior to being diagnosed. It was not until all of these things had transpired and my neuro had more data to look at, including an MRI that began to "look more like MS" that I was given an MS diagnosis.

          I can't answer your question. I am simply not qualified. Your symptoms might be MS. They might not be.
          ~ Faith
          MSWorld Volunteer -- Moderator since JUN2012
          (now a Mimibug)

          Symptoms began in JAN02
          - Dx with RRMS in OCT03, following 21 months of limbo, ruling out lots of other dx, and some "probable stroke" and "probable CNS" dx for awhile.
          - In 2008, I was back in limbo briefly, then re-dx w/ MS: JUL08
          .

          - Betaseron NOV03-AUG08; Copaxone20 SEPT08-APR15; Copaxone40 APR15-present
          - Began receiving SSDI / LTD NOV08. Not employed. I volunteer in my church and community.

          Comment


            #6
            Go have an MRI. I don’t know; your doctor doesn’t know; no one here knows. Good luck.

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