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How do I know if I have Miller Fisher Syndrome?

What signs or symptoms may make you suspect you may have Miller Fisher Syndrome. People who have experience in Miller Fisher Syndrome offer advice of what things may make you suspicious and which doctor you should go to to receive treatment

Do I have Miller Fisher Syndrome?

How to Determine if You Have Miller Fisher Syndrome?


Miller Fisher Syndrome (MFS) is a rare neurological disorder that affects the nerves controlling movement and coordination. It is considered a variant of Guillain-Barré Syndrome (GBS) and is characterized by a specific set of symptoms. If you suspect you may have MFS, it is important to consult with a healthcare professional for a proper diagnosis. However, there are several key signs and symptoms associated with MFS that can help you determine if you should seek medical attention.



1. Triad of Symptoms:


The hallmark of Miller Fisher Syndrome is the presence of a triad of symptoms, which includes:



  • Ophthalmoplegia: Weakness or paralysis of the eye muscles, leading to double vision or difficulty moving the eyes.

  • Ataxia: Lack of coordination and unsteady movements, often affecting balance and gait.

  • Areflexia: Absence or reduced reflexes, such as the knee-jerk reflex.



2. Onset and Progression:


MFS typically develops rapidly over a period of hours to days. The symptoms may worsen for a week or two before stabilizing. It is important to note that the severity and progression of symptoms can vary from person to person.



3. Additional Symptoms:


In addition to the triad of symptoms, individuals with MFS may experience other neurological manifestations, such as:



  • Facial weakness or paralysis

  • Difficulty speaking or swallowing

  • Sensory abnormalities, such as numbness or tingling



4. Recent Infection:


MFS is often preceded by a respiratory or gastrointestinal infection, such as a cold or diarrhea. The symptoms of MFS typically appear within a few days to weeks after the infection.



5. Diagnostic Tests:


To confirm a diagnosis of MFS, a healthcare professional may perform various tests, including:



  • Neurological examination: Assessing reflexes, eye movements, coordination, and muscle strength.

  • Lumbar puncture: Collecting a sample of cerebrospinal fluid to check for abnormalities.

  • Nerve conduction studies: Evaluating the electrical activity and function of the nerves.

  • Antibody testing: Checking for the presence of specific antibodies associated with MFS.



If you suspect you have Miller Fisher Syndrome based on the symptoms mentioned above, it is crucial to consult a healthcare professional for an accurate diagnosis. Early detection and treatment can help manage the symptoms and improve outcomes.


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I was diagnosed in 1997 and in 2009.  I have fully recovered.  Both times the onset was a sinus infection.  I received my care from the Mayo Clinic, Rochester MN.

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