Dr. Bateman Keynote at Long COVID and Fatiguing Illness ECHO
As part of the Long COVID and Fatiguing Illness Recovery Program ECHO, Dr. Bateman has been asked to speak as the ME/CFS expert for this session in honor of awareness […]
As part of the Long COVID and Fatiguing Illness Recovery Program ECHO, Dr. Bateman has been asked to speak as the ME/CFS expert for this session in honor of awareness […]
We are holding the 4th annual virtual BHC awareness event on Tuesday, May 9th at noon MDT! The Reflections of ME/CFS, FM, & LC event will include a line-up of […]
The Bateman Horne Center and Solve M.E. are pleased to host a free, comprehensive webinar series, "Severe ME/CFS: Care, Rights and Research." Register Here 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 […]
The Bateman Horne Center and Solve M.E. are pleased to host a free, comprehensive webinar series, "Severe ME/CFS: Care, Rights and Research." Register Here Legal Planning for Severe M.E.: Steps to Take if You Need Help Managing Life and Decisions The second webinar in our series focuses on the multifaceted legal considerations faced by people […]
The Bateman Horne Center and Solve M.E. are pleased to host a free, comprehensive webinar series, "Severe ME/CFS: Care, Rights and Research." Register Here Wednesday, December 4: Medical Explore insights from healthcare professionals on the unique challenges and strategies involved in caring for individuals with severe ME/CFS, including treatment approaches and navigating the medical system. […]
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" Register Here 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 […]