Hunter-Hopkins Center, PLLC

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  • Posts tagged "Fibromyalgia"

ME Letter June 2014

July 20, 2014 / Charles W. Lapp, MD / News

This Month’s Contents Immunomodulators Creatine May Improve Muscle Function Checking the Cost of Medications Getting Some Help At Home Housekeeping Issues Emails under the new HIPAA Bring medications with you to the office Confirm your appointment when you get a “reminder call” The Use of Immunomodulators in CFS/ME/FM A subset of individuals with CFS/ME/FM experience […]

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Ampligen, CFS, Coping with CFS/ME/FM, Dr. Lapp, Fibromyalgia, Immunomodulators, ME Letter

I Sweat A Lot. What Causes That?

February 16, 2012 / Charles W. Lapp, MD / Ask The Doctor

I sweat a lot. What causes that? Excess perspiration is a common symptom of both CFS/ME and FM. The etiology is not clear. Dysautonomia is common in CFS/ME/FM, and may cause perspiration (diaphoresis). Also, PWCs have a narrow comfort range for environmental temperatures. In other words, it is easy for a PWC to get overheated […]

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Chronic Fatigue Syndrome, Coping with CFS/ME/FM, Fibromyalgia

I Never Get A Good Night’s Sleep

February 16, 2012 / Charles W. Lapp, MD / Ask The Doctor

I never seem to get a good night’s sleep any more. What can you tell me about sleep? Sleep is one key to improvement in CFS, ME, and FM. Without sufficient restful sleep even normal healthy people feel tired, achy, and irritable; so imagine how PWCs would feel! There are at least 8 characteristics of […]

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abnormal sleep, CFS Treatment, Chronic Fatigue Syndrome, Fibromyalgia, FM, ME

What Should I Tell Friends About CFS/ME/FM?

February 16, 2012 / Charles W. Lapp, MD / Ask The Doctor

What should I tell friends or employers who ask about CFS/ME/FM? Don’t you get tired of explaining?! If you explain “Chronic Fatigue Syndrome” the likely response is “oh yeah, I get tired a lot myself,” or “isn’t that the ‘Yuppie Flu’?” Both responses are justifiable grounds for homicide, in my opinion! At worst the word […]

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ADA, Chronic Fatigue Syndrome, Fibromyalgia, Myalgic Encephalomyelitis

Ask The Doctor – Please Read Before Posting

February 16, 2012 / Charles W. Lapp, MD / Ask The Doctor

Get the facts on CFS/ME/FM. Ask the Doctor is your opportunity to get questions about Chronic Fatigue Syndrome, Myalgic Encephalomyelitis and Fibromyalgia answered by Dr. Lapp and Dr. Black at Hunter-Hopkins Center. [approved]Please feel free to submit questions for Dr. Lapp or Dr. Black to answer using the comment form or email us at drlapp@drlapp.net. […]

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CFS, Chronic Fatigue Syndrome, Dr. Black, Dr. Lapp, Fibromyalgia, Myalgic Encephalomyelitis

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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