August 16, 2019

U.S School Nurses, Teachers & Counselors can now take Continuing Education Course about Pediatric ME/CFS

August 16, 2019 No Comments

School nurses, counselors, social workers or teachers in any U.S. state can now earn earn 3.25 Continuing Education credits (CNE) for completing a course on pediatric myalgic encephalomyelitis / chronic fatigue syndrome (ME/CFS). The course is titled, ““Why Can’t This Child Get to Class? Learn How ME/CFS Keeps Youth from Attending School.” The course features Dr, Peter Rowe,

Australia to Launch its First ME/CFS Biobank and Patient Registry

August 16, 2019 1 Comment

Australian philanthropic trust the Mason Foundation will establish the first Australian national ME/CFS biobank and patient registry, with a $1 million grant. The grant consists of two components: the biobank and patient registry, and a research project which uses the samples stored in the biobank. This is significant news for the Australian ME/CFS community, and has been picked up by mainstream media.

Greater London Authority Unrest screenings to raise awareness of ME

August 16, 2019 No Comments

The Greater London Authority’s offices have held two Unrest screenings over the past few months to raise awareness of myalgic encephalomyelitis (ME). The screenings, held for staff, took place at Union Street and City Hall, and were part of ME Awareness Week and the #MillionsMissing campaign. Officers and staffers attended the two screenings, held in

Day: August 16, 2019

U.S School Nurses, Teachers & Counselors can now take Continuing Education Course about Pediatric ME/CFS

Australia to Launch its First ME/CFS Biobank and Patient Registry

Greater London Authority Unrest screenings to raise awareness of ME