Exciting news! The U.S. ME/CFS Clinician Coalition has released new resources for people with ME/CFS to bring to their health care providers for diagnosis, testing, and treatment recommendations.
Read the Coalition Recommendations Announcement here.
The resources include a document on testing recommendations and a document on treatment recommendations to help patients and their healthcare providers with the overall care and management of ME/CFS.
OMF’s goal is to empower caregivers and people living with ME/CFS to manage their health today while we search for tomorrow’s answers. We hope you find these new documents to be helpful in navigating the complex world of ME/CFS.
Be sure to also check out OMF’s Resource Center! This webpage includes parent resources, information to share with your doctor, general information on ME/CFS, and more. We will continue to share with the community whenever the page has been updated with new, verified information.
About The U.S. ME/CFS Clinician Coalition:
The U.S. ME/CFS Clinician Coalition is a group of U.S. clinical disease experts who have collectively spent hundreds of years treating thousands of ME/CFS patients.
They have authored primers on clinical management, served on CDC medical education initiatives, and are actively involved in ME/CFS research. OMF is proud that Ronald G. Tompkins, MD, ScD, OMF Chief Medical Officer, is one of the U.S. ME/CFS Clinician Coalition members.
If you are able, please consider contributing to our effort to uncover research-based answers.
Help us improve the quality of life for all sufferers of ME/CFS and other chronic complex diseases, such as Post Treatment Lyme Disease Syndrome and Fibromyalgia.
