From Emerge Australia.

Emerge Australia conducted a second Health and Wellbeing Survey of people living with myalgic encephalomyelitis/ chronic fatigue syndrome (ME/CFS) in 2019.

An impressive 1,055 participants from around Australia answered 60 questions covering demographics, caring responsibilities, ME/CFS onset and symptom experience, access to healthcare and other services, and the effect of living with ME/CFS on social and economic circumstances. They also provided insight on the greatest barriers faced in accessing healthcare services and identified opportunities for improvement.

Lifelong Lockdown: Lessons Learned from the Health and Wellbeing Survey of Australians Living with ME/CFS 2019  was published in October 2020. Our findings paint a detailed picture of the experiences of people living with myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS).

To read the rest of this story, click on the link below:

Link to Australian ME Survey