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Severe ME/CFS Care, Rights, and Research
The Bateman Horne Center and Solve M.E. are pleased to host a free, comprehensive webinar series, “Severe ME/CFS Research: Removing Barriers to Access”
Tuesday, January 21: Research
Traditional research often excludes people with severe ME/CFS, who make up nearly 25% of the community. Their absence limits our understanding of the disease—but patient advocates are driving change to make research more accessible and inclusive. Join BatemanHorneCenter and Solve ME Initiative for an insightful discussion on:
✔️ Barriers to research participation for severe ME patients
✔️ How patient advocates and researchers are improving accessibility
✔️ Tips for patients considering participation in clinical studies
The series will be recorded and posted on our YouTube channel.
The content provided by Solve M.E. and the Bateman Horne Center in this webinar is for informational purposes only and does not constitute legal or medical advice. Viewers are encouraged to consult with qualified legal or medical professionals for specific advice tailored to their individual circumstances.
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.