Watch! Solve M.E. and Bateman Horne Center Severe ME/CFS Webinar Series Session 1: Caregiving
Solve M.E. and Bateman Horne Center (BHC) recently co-hosted a webinar on caregiving and Severe M.E. for the benefit of patients and caregivers navigating life with severe ME/CFS. The webinar […]
Solve M.E. and Bateman Horne Center Partner for Webinar Series: “Severe ME/CFS: Care, Rights, and Research”
In a continuing effort to support the ME/CFS community, Solve M.E. and Bateman Horne Center (BHC) will launch a groundbreaking four-part webinar series titled, “Severe ME/CFS: Care, Rights, and Research.” […]
Severe ME/CFS: Care, Rights, and Research Webinar Series — Research (Pt. 4 of 4)
ME/CFS has a broad spectrum of severity, with some able to work while others require total care and support. People living with Severe ME are often confined to their beds […]
Severe ME/CFS: Care, Rights, and Research Webinar Series — Medical Care (Pt. 3 of 4)
ME/CFS has a broad spectrum of severity, with some able to work while others require total care and support. People living with Severe ME are often confined to their beds […]
Severe ME/CFS: Care, Rights, and Research Webinar Series — Legal Rights (Pt. 2 of 4)
ME/CFS has a broad spectrum of severity, with some able to work while others require total care and support. People living with Severe ME are often confined to their beds […]
Severe ME/CFS: Care, Rights, and Research Webinar Series — Caregiving (Pt. 1 of 4)
ME/CFS has a broad spectrum of severity, with some able to work while others require total care and support. People living with Severe ME are often confined to their beds […]
Solve Author Series: Dr. Peter Rowe Discusses “Living Well with Orthostatic Intolerance: A Guide to Diagnosis and Treatment”
Orthostatic intolerance (OI) describes a group of circulatory disorders whose symptoms are characterized by a dramatic drop in blood flow to the brain when people are sitting for long periods […]
Solve Spotlight: Writer Nadine Sander-Green in Conversation with Joe Komsky
Before developing ME/CFS, Canadian writer Nadine Sander-Green was an avid adventurer, canoeing down rapids, mountain-biking along rugged trails, and skiing through waist-deep powder. Post-diagnosis, she’s written in detail about her […]
Dr. Susan Levine’s Responses to Follow-Up Webinar Questions
In Part Two of her follow-up to our March 17 webinar, Dr. Susan Levine, founder of the Medical Office of Susan M. Levine, M.D., responds to a wide range of patient questions that time did not was not able to field during the webinar. Read More…
Dr. Susan Levine’s Responses to Follow-Up Webinar Questions—Part I
On March 17, the Solve ME/CFS Initiative hosted a webinar with Dr. Susan Levine, founder of the Medical Office of Susan M. Levine, M.D., called, “The Future of ME/CFS.” Read More…
