This National Clinical Trials Day, the Bateman Horne Center calls for a shift in how we fund and value patient-centered research. On National Clinical Trials Day, we celebrate the scientific backbone of modern medicine: the clinical trial. But while many people...
A Roadmap to Better Care: Clinical Care Guide for ME/CFS, Long COVID & Infection-Associated Chronic Conditions Introducing the Clinical Care Guide for ME/CFS, Long COVID & Infection-Associated Chronic Conditions For individuals living with ME/CFS, Long COVID,...
The Medical Education Resource Center (MERC) was founded by Open Medicine Foundation and Bateman Horne Center to inform clinicians about ME/CFS and other complex infection-associated chronic conditions.
Bateman Horne Center Bridges Borders to ME/CFS Care: A Conversation with Dr. Hacohen and Jennifer Bell, CNP Bridging Borders to Advance ME/CFS Care: A Conversation with Dr. Gourgy-Hacohen and Nurse Practitioner, Jennifer Bell At the Bateman Horne Center (BHC), our...
Borrowing and Holding Onto Hope: A Journey Through Long COVID and ME/CFS Living with Long COVID and ME/CFS means facing uncertainty, loss, and often, unimaginable suffering. But it also means discovering resilience in ways few can understand. One patient’s story...
Are research and education on Long COVID translating into better treatment and care for those with Long COVID, ME/CFS, and related conditions? The answer is yes—though progress is painfully slow. Still, I see significant forward movement, and I remain hopeful. The...
Far From Rare: A Common Disease Hidden in Plain Sight Why ME/CFS Needs to be Recognized Now February often brings conversations about rare diseases—conditions affecting fewer than 200,000 people in the U.S. ME/CFS doesn’t fit that definition. Yet, we chose to...
The emergence of SARS-CoV-2, the virus responsible for COVID-19, swept across the globe with an unparalleled speed and severity. As a researcher dedicated to understanding how viral infections lead to chronic illness, I knew this pandemic would have far-reaching...
Promising Clinical Trial Results: Advancing ME/CFS and Long COVID Treatment by Suzanne Vernon, PhD, Director of Research At the Bateman Horne Center (BHC), we are committed to finding effective treatments for myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS)...
Practical Tools for Managing ME/CFS: Insights from Amy Mooney, MS OTR/L and caregiver Caring for a teenager with severe ME/CFS has been a life-changing journey for me, both as a mother and as an occupational therapist. The complexities of this condition—where energy...
This National Clinical Trials Day, the Bateman Horne Center calls for a shift in how we fund and value patient-centered research. On National Clinical Trials Day, we celebrate the scientific backbone of modern medicine: the clinical trial. But while many people...
A Roadmap to Better Care: Clinical Care Guide for ME/CFS, Long COVID & Infection-Associated Chronic Conditions Introducing the Clinical Care Guide for ME/CFS, Long COVID & Infection-Associated Chronic Conditions For individuals living with ME/CFS, Long COVID,...
The Medical Education Resource Center (MERC) was founded by Open Medicine Foundation and Bateman Horne Center to inform clinicians about ME/CFS and other complex infection-associated chronic conditions.
Bateman Horne Center Bridges Borders to ME/CFS Care: A Conversation with Dr. Hacohen and Jennifer Bell, CNP Bridging Borders to Advance ME/CFS Care: A Conversation with Dr. Gourgy-Hacohen and Nurse Practitioner, Jennifer Bell At the Bateman Horne Center (BHC), our...
Borrowing and Holding Onto Hope: A Journey Through Long COVID and ME/CFS Living with Long COVID and ME/CFS means facing uncertainty, loss, and often, unimaginable suffering. But it also means discovering resilience in ways few can understand. One patient’s story...
Are research and education on Long COVID translating into better treatment and care for those with Long COVID, ME/CFS, and related conditions? The answer is yes—though progress is painfully slow. Still, I see significant forward movement, and I remain hopeful. The...
Far From Rare: A Common Disease Hidden in Plain Sight Why ME/CFS Needs to be Recognized Now February often brings conversations about rare diseases—conditions affecting fewer than 200,000 people in the U.S. ME/CFS doesn’t fit that definition. Yet, we chose to...
The emergence of SARS-CoV-2, the virus responsible for COVID-19, swept across the globe with an unparalleled speed and severity. As a researcher dedicated to understanding how viral infections lead to chronic illness, I knew this pandemic would have far-reaching...
Promising Clinical Trial Results: Advancing ME/CFS and Long COVID Treatment by Suzanne Vernon, PhD, Director of Research At the Bateman Horne Center (BHC), we are committed to finding effective treatments for myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS)...
Practical Tools for Managing ME/CFS: Insights from Amy Mooney, MS OTR/L and caregiver Caring for a teenager with severe ME/CFS has been a life-changing journey for me, both as a mother and as an occupational therapist. The complexities of this condition—where energy...
Lucinda Bateman, MD, is a renowned clinician, researcher, and educator. Her Johns Hopkins University Medical School training instilled an approach to care that she has employed throughout her career - the patient comes first and the unknown or unexplained does not equate to a lack of proper and compassionate care. Since starting her own practice in 2000, she has served on six boards or committees, been the principal investigator for 45 studies, authored/coauthored 40 journal articles, served as adjunct instructor and adjunct assistant professor in the University of Utah Departments of Preventative Medicine, Internal Medicine, and Anesthesiology, and lectured around the world.