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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: Care, Rights and Research.”
The first webinar on Wednesday, Oct. 9 focuses on Caregiving and will discuss navigating systems, role changes, daily care, caregiver mental health and maintaining healthy relationships. The series will be recorded and posted on our YouTube channel.
Panelists include:
Galen Warden, mother to an adult son with severe ME
Amy Mooney, mother to a teen daughter with severe ME
Kim Moy, wife of husband has severe ME
Kyle Kitzmiller, husband to a wife (Physics Girl, Dianna Cowern) with severe ME
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.