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. […]

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

ME Letter March 2012

April 7, 2012 / Charles W. Lapp, MD / News

This Month’s Contents Ask The Doctor Open Medicine Institute considers Ampligen, rituximab Six Month Disability Follow-Ups Recommended $50 Bonus for Referring to HHC! CFS/ME/FM Treatment Website A New Imaging Technique Reveals Brain Wiring Having Trouble Getting or Affording Health Insurance? Ask The Doctor PWCs often want to ask general questions about CFS/ME or FM. Now […]

Ampligen, CFS & FM Self Help, Disability, PCIP, Rituximab

ME Letter December 2011

December 26, 2011 / Charles W. Lapp, MD / News

Contents New Research Opportunities Clinical Assessment of CFS Rituximab Fatigue Self-Help Skills Pain Is A Problem! Disposing of Medications Hunter-Hopkins Is On Facebook Ampligen Update Happy Holidays, Merry Christmas, and best wishes for 2012 New Research Opportunities Hunter-Hopkins has joined with several well-known practices to form the Open Medicine Institute. Using EMR (Electronic Medical Records) […]

Ampligen, CFS, CFS Treatment, Chronic Fatigue Syndrome, ME, Myalgic Encephalomyelitis, Pain Meds, Rituximab

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

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 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.

Hunter-Hopkins Center, PLLC

December 2012 ME-Letter

ME Letter March 2012

ME Letter December 2011

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