Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS)

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Displaying 1-2 out of 2 doctors available

Last Name Initial: G

  1. Stephanie L. Grach, M.D., M.S.

    Stephanie L. Grach, M.D., M.S.

    1. Internist
    1. Rochester, MN
    Areas of focus:

    Fibromyalgia, Post-COVID-19 syndrome, POTS, Myalgic encephalomyelitis/chronic fatigue syndrome

  2. Alexander E. Gurfinkel, M.D.

    Alexander E. Gurfinkel, M.D.

    1. Pediatrician
    1. Rochester, MN
    Areas of focus:

    Telemedicine, General pediatric care, Supplements counseling, Complex care coordination, Anticipatory guidance, Genetic... disorder, Dysautonomia, Neurodevelopmental disorder, Dizziness, POTS, Orthostatic hypotension, Orthostatic intolerance, Syncope, Headache in children, Myalgic encephalomyelitis/chronic fatigue syndrome, Rare disorders, Failure to thrive

By Mayo Clinic Staff
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Diagnosis & treatment
May 11, 2023
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Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS)

Research: It's all about patients

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Joseph Sirven, M.D., Professor of Neurology, Mayo Clinic: Mayo's mission is about the patient. The patient comes first. So the mission and research here is to advance how we can best help the patient, how to make sure the patient comes first in care. So in many ways, it's a cycle. It can start with as simple as an idea worked on in a laboratory, brought to the patient bedside, and if everything goes right — and let's say it's helpful or beneficial — then brought on as a standard approach. And I think that is one of the unique characteristics of Mayo's approach to research — that patient-centeredness — that really helps to put it in its own spotlight.