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  • Articles posted by Charles W. Lapp, MD (Page 4)

Is there one climate more conducive to good health?

July 14, 2014 / Charles W. Lapp, MD / Ask The Doctor

Q:            Maureen C wrote, “My husband and I are fortunate to be able to live wherever we would like.  Given my medical situation, where is the best location for me to live?” A:            There is not one best place to live in general, because everyone has different needs and desires. Some prefer cold climates and […]

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Why Do Antibiotics Make Me Feel Better?

June 28, 2014 / Charles W. Lapp, MD / Ask The Doctor

Many PWCs have experienced improvement of symptoms following antibiotic treatment for other conditions.  The natural questions then are why?  And should I continue to take antibiotics? The first answer is simple.  Antibiotics may “work” in more than one way.  Yes, they might be treating some hidden infection in the body.  But antibiotics have other ameliorating […]

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Do I Have Lyme, CFS/ME, or Both?

June 28, 2014 / Charles W. Lapp, MD / Ask The Doctor

On a regular basis PWCs return to me with a new diagnosis of Lyme Disease.  My main concern in such a situation is whether the diagnosis is accurate and treatment appropriate. Lyme Disease can be a trigger for CFS/ME just as can EBV, HHV6, and other infections [Steere AC, JAMA 1993].  That’s why we request […]

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IACFS 2014 Summary

April 4, 2014 / Charles W. Lapp, MD / News

IACFS International Conference Summary 11th International IACFS/ME Conference Parc 55 Wyndham Union Square Hotel San Francisco CA March 20-23, 2014 The theme for this biennial IACFS conference was “Translating Science into Clinical Care,” which implies that most papers would address treatments and management schemes aimed at improving the care of persons with CFS/ME and FM. […]

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IACFS Conference

ME Letter March 2014

March 30, 2014 / Charles W. Lapp, MD / News

This Month’s Contents Introduction – Dr. Ian Lipkin Therapy Immunology Virology / Infections Exercise Testing Prognosis Pediatrics Brain Research Severely Ill Biobanking Summary – Dr. Anthony Komaroff Closing Statement – Dr. C. W. Lapp 11th International IACFS/ME Conference Parc 55 Wyndham Union Square Hotel March 20-23, 2014 The theme for this biennial IACFS conference was […]

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CFS, CFS Treatment, Chronic Fatigue Syndrome, IACFS, IACFS Conference, ME Letter, Myalgic Encephalomyelitis

Candida Infections and CFS/ME/FM

January 26, 2014 / Charles W. Lapp, MD / Ask The Doctor

Cally L. wrote me, “I’ve been reading about candida overgrowth. Is this something you think is valid? Something I should be tested for?” A:      Candida overgrowth is a common phenomenon in persons with CFS/ME/FM, probably because NK Cell Activity is low in most patients and it is the NK Cells that are thought to help […]

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Late Lyme versus ME/CFS

December 7, 2013 / Charles W. Lapp, MD / Ask The Doctor

Q: Nancy H asks, “Do you treat Lyme patients any differently than a patient with ME/CFS or FM?” A: While there is no known cause of ME/CFS or FM, it is well-acknowledged that infections trigger many cases. While EB Virus (mononucleosis) is probably the most common, I have also seen ME/CFS and FM apparently triggered […]

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ME Letter September 2013

October 16, 2013 / Charles W. Lapp, MD / News

This Month’s Contents Cognitive Problems in CFS/ME Seeking Bedbound Patients More Affordable Medications Housekeeping Issues Emails under the new HIPAA Bring your medications to the office with you Cognitive dysfunction in CFS/ME CFS/ME is characterized by four core symptoms: exertional fatigue, muscle pain or headache, sleep disruption or non-restorative sleep, and cognitive dysfunction. Cognitive problems […]

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CFS, Cognitive Dysfunction, ME Letter

December 2012 ME-Letter

December 27, 2012 / Charles W. Lapp, MD / News

Contents Clinical Assessment of CFS / Thanks! Rituximab Hunter-Hopkins Chat On Facebook Ampligen Update Confirm Your Appointment! Happy Holidays, Merry Christmas, and best wishes for 2013 Research Continues on the Clinical Assessment of CFS For over one year Hunter-Hopkins has been participating in a Centers for Disease Control contract study, the Clinical Assessment of CFS.  […]

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Ampligen, CFS, CFS Treatment, Dr. Black, Dr. Lapp, ME Letter, Rituximab

ME Letter September 2012

October 3, 2012 / Charles W. Lapp, MD / News

This Month’s Contents Lexington SC Lecture on October 8 Order Your Physician a Primer from the IACFSME Don’t Forget to Vote! Order Your Absentee Ballot NOW Patient Commerce Site on Facebook Ask The Doctor $50 Bonus for Referring to HHC! Sorry We’re Late … Lexington SC Seminar Planned for October 8 Dr. Lapp will be […]

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IACFSME, ME Letter
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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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