Hunter-Hopkins Center, PLLC

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  • 2012
  • July

June 2012 ME-Letter

July 18, 2012 / Charles W. Lapp, MD / News

This Month’s Contents Kentucky Seminars on August 17 and 18 New Physician Primer from the IACFSME New Free-Access Fibromyalgia Management Guide for Primary Care Doctors Risky Business – A Possible Relation of CFS to Cancer Open Medicine Institute NYC Meeting Ask The Doctor $50 Bonus for Referring to HHC! Trouble Getting or Affording Health Insurance? […]

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Does “Brain Fog” Ever Go Away?

July 18, 2012 / Charles W. Lapp, MD / Ask The Doctor

Q:           Adam W asked about cognitive problems:  “Does the ‘brain fog’ or ‘spaced out’ symptom of CFS ever resolve?” A:            As with most CFS symptoms, cognitive dysfunction waxes and wanes. One report suggests that IQ falls during a flare of cognitive dysfunction, and our personal experience is that memory, attention, processing speed, and other parameters […]

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The Story of Hunter-Hopkins

The Hunter-Hopkins name derives from two individuals who were memorialized because of the invaluable lessons they taught to Dr. Lapp.

Linda Hopkins

Linda Hopkins presented to the emergency room complaining that she could not breath when she nodded off to sleep. As a result she had not slept in weeks. Other physicians had discounted her story as impossible, but Linda and her mother convinced Dr. Lapp to look into it further. Linda was hospitalized and monitored overnight. Sure enough, as soon as she nodded off, Linda went into respiratory arrest – a very severe form of sleep apnea now known as “Ondine’s Curse.” Once the problem was identified, Linda was fitted with a respirator to be used while sleeping. Lesson learned: listen to the patient.

Allison Hunter

Allison Hunter was diagnosed with Chronic Fatigue Syndrome, but lived in Australia, where the providers of socialized medicine ‘did not believe’ in the diagnosis. As a result she was misnamed a malingerer, hysterical, or Munchhausen – a term reserved for individuals who purposely pretend to be sick. When Alli developed convulsions they were attributed to this ‘phantom illness’ and went untreated. As a result, she died during a grand mal seizure. Lessons learned: (1) diligently look into all complaints and don’t discount them, and (2) don’t trust socialized medicine.

Allison’s parents went on to found the Allison Hunter Memorial Foundation, which has promoted CFS throughout the Pacific Basin and provides superb seminars for practitioners to learn more about CFS and FM.

So we have admired and memorialized these two young women who taught us much about the importance of diligence and listening to the patient.

Our Mission

We are dedicated to exceeding our patients’ expectations by providing individualized, compassionate, empathetic, and timely care. Our goal is to improve the quality of our patients’ lives by providing the highest quality of advanced evidence-based diagnosis and treatment available.

The patient is our first priority; conquering CFS/ME/FM is our ultimate goal.

The Banyan Tree

We chose the banyan tree to represent our practice because the resilient and long lived banyan offers its shade as a safe and sheltered place for weary travelers and the banyan’s distinctive habit of sprouting new supportive roots from its branches reminds our clients to find and accept support for themselves.

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