![]() ME/CFS South Australia Inc supports the needs of sufferers of Myalgic Encephalomyelitis, Chronic Fatigue Syndrome and related illnesses. We do this by providing services and information to members. Disclaimer ME/CFS South Australia Inc aims to keep members informed of various research projects, diets, medications, therapies, news items, etc. All communication, both verbal and written, is merely to disseminate information and not to make recommendations or directives. Unless otherwise stated, the views expressed on this Web site are not necessarily the official views of the Society or its Committee and are not simply an endorsement of products or services. |
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Researchers At Columbia University Publish First ME/CFS Study Of Proteins In BloodWednesday 30 September 2020
From the Solve ME/CFS Initiative:
RESEARCHERS AT COLUMBIA UNIVERSITY PUBLISH FIRST ME/CFS STUDY OF PROTEINS IN BLOOD In 2018, Solve M.E. provided partial funding to Columbia University Mailman School of Public Health’s Center for Infection & Immunity (CII), led by W. Ian Lipkin, MD, for an exploratory study of blood plasma proteins in a group of ME/CFS patients and controls. We’re excited to report that the research team, which also included Columbia physician-scientist Mady Hornig, MD, and a number of other leaders in the ME/CFS field, published their findings in PLOS One at the end of July 2020. Using powerful new technologies that can measure a large number of proteins simultaneously, researchers were able to identify a group of proteins that distinguished people with ME/CFS from controls. You can get a quick breakdown below and read the full study here. Don’t miss this! ME/CFS blogger and thought leader Cort Johnson published an article about the study findings and future research directions. He also talks to Dr. Ian Lipkin (who is recuperating from COVID-19) about joining the “long hauler” community and what we know about the connection between long COVID and ME/CFS so far.
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