The Lean Test:
This study aims to assess the clinical utility of the Lean Test as well as the impact of orthostatic stress on the metabolome and the epigenome. Study participants will complete a supervised Lean Test with a randomly selected subset of study participants providing blood samples before and after testing. ME/CFS patients, COVID-19 long haulers with PACS (post-acute COVID-19 syndrome) and healthy controls will be needed to complete this study.
Recruitment of ME/CFS patients, COVID-19 long haulers, and healthy controls will be held at the following sites:
Bateman Horne Center (Salt Lake City, UT)
Clinical Trials (Domestic and International Opportunities)
The NIH U.S. National Library of Medicine updates their database with on-going clinical trials worldwide. You can sort by status of the trial, eligibility criteria, location, and topic.
The ME/CFS community has such strength in supporting each other as we navigate towards answers for this devastating disease. These are just a few of the patient forums available to find out more information on advocacy and learn about each other's journeys.
#MEAction is a grassroots, international organization that provides a platform to empower people with ME and related conditions and advocates for patients in the pursuit of health equality. Their mission is to continually build community and provide a voice for patients, families, and allies of ME, based on the belief that while it may be difficult to individually advocate, making activism accessible can amass a louder voice for the community as a whole.
Solve ME/CFS Initiative is a non-profit disease organization that works to accelerate the discovery of safe and effective treatments for ME/CFS, strives for an aggressive expansion of research funding that will lead to a cure, and seeks to engage the entire ME/CFS community in research and advocacy. Solve M.E. serves patients and researchers alike, acting as an information and data hub for the ME/CFS community.
The You + ME Registry and Biobank is a collection of patient-reported data and biological samples (e.g. blood) from people living with myalgic encephalomyelitis (also known as chronic fatigue syndrome or ME/CFS), people with long COVID, and control volunteers. A large, rich dataset gathered over time from thousands of people will drive discovery towards potential treatments and cures. Join the You + Me Registry and help find a cure.
The Coalition is committed to improving clinical care for patients with ME/CFS by advancing best clinical practices, providing education for the medical community, expanding the pool of medical providers with strong expertise in ME/CFS, and providing clinical insights for researchers.
Have something to say? Need some more information? Here are some of the online places you can visit to read about what others are experiencing, share what you have encountered on your own path, or review some of the resources that may have some additional information.
Phoneix Rising provides people with ME/CFS information to support their health and well-being. They publish articles and a newsletter, maintain the largest ME/CFS forum in the world, and have the biggest database of information about ME/CFS on the web.
CDC: What is ME/CFS?
HHS Office on Women's Health: Chronic fatigue syndrome
National Academies of Science: Beyond ME/CFS: Redefining an Illness (publication)
NIH Director's Blog: Moving Towards Answers in ME/CFS
NINDS: Common Data Elements (CDE)
RTI: RTI International