Listen to blog Listen. Believe. Do No Harm. An occupational therapist's guidance for caring well for people with severe ME/CFS For someone with severe myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS), being sick is a full-time job. Light, sound,...
Severe and Very Severe ME/CFS
Practical Tools for Managing ME/CFS: Insights from Amy Mooney, MS OTR/L and Caregiver
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...
Severe ME/CFS Community: You Are Seen, Heard and Valued
Dear Community, Although today is designated for remembering and reflecting on those with Severe ME/CFS, please know that you are in my thoughts every day. I have a photograph of a piece of artwork submitted for ME Awareness Day a couple of years ago. It is entitled...
How to Be a Demanding Diplomat as a Severe ME/CFS Caregiver
Galen Warden is the mother of an adult son with severe ME/CFS. Bateman Horne Center partnered with her to provide essential guidance on caring and advocating for individuals with ME/CFS. This blog post includes: Galen's video presentation Galen's presentation slides...




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.