Impact of increased exercise/activity
From: "Emerge Australia Health and Wellbeing Survey 2018"
emerge.org.au/emerge-austral
#MEcfs #CFS #MyalgicE #MyalgicEncephalomyelitis #ChronicFatigueSyndrome
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The statistics on graded exercise are very confusing.
Page 42 says 16% of those with severe/very severe symptoms found GET very helpful, (32% of the mild/moderate)
whereas on page 39 only 3% of the severe/very severe say GET helps them feel better (8% of the mild/moderate)
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#CFS Hi Tom, if other researcher would stop stealing my research and claiming it to be theirs I could tell them a lot more about CFS and exercise, as well as many other ways of treating it. But they keep guessing and getting it wrong for the past 40 years.
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Rather than sharing this image, which is taken from the report and likely to lose attribution if people save it and share it elsewhere, please share this infographic:
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I shared that image previously
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Results are now available for @EmergeAus Health and Wellbeing Survey 2018
emerge.org.au/emerge-austral
Full 77-page report: emerge.org.au/wp-content/upl
#MEcfs #CFS #MyalgicE #MyalgicEncephalomyelitis #ChronicFatigueSyndrome
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I think the five percent probably are not living with MECFS because everytime many of us do exercise is a risk for our energy and our activities. I send you a hug.
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