Australia: Write to North Sydney by-election candidates
November 30, 2015
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Australia: Write to the North Sydney by-election candidates about ME.
Author: Sasha Nimmo
Aust Senator questions government on lack of action on ME
November 16, 2015
2 Comments
Australia’s Senator Ludlam asks Department of Health what they do for people with ME.
PACE trial's 'sister' study overlooked
November 10, 2015
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In his Virology blog, David Tuller examines results of ‘sister’ to the PACE trial
Australia: What is the fuss? Make a video for the Medical Research Fund
October 19, 2015
1 Comment
Maka a video about ME and make a fuss! (Australia)
Muscle defect studied in UK
October 18, 2015
1 Comment
Patients in the UK’s north east will benefit from muscle abnormality research put into action via hospitals.
Visionary viral disease treatment needs funding
October 15, 2015
9 Comments
Imagine a drug that could treat almost any viral disease. We may only be a few years’ away, thanks to Dr Rider at MIT.
Give your Patient Opinion (UK, IR & Aus)
September 25, 2015
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Independent organisation Patient Opinion wants to hear feedback on healthcare services from patients in Australia, Ireland and the UK.
Treadmill test shows who Ampligen may help
September 24, 2015
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Hemispherx Biopharma research shows that CFS patients who can perform more than 9 minutes on a treadmill are more likely to benefit from Ampligen.
Chronic Fatigue Syndrome Advisory Committee (USA) recommendations
September 21, 2015
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USA’s CFS Advisory Committee wants bigger research, aimed at finding diagnostic tests, using Canadian Consensus Criteria and private-public partnerships to find drug treatments. It asks for $250 million annually, estimating ME/CFS costs the US up to $24 billion.
Study shows immune differences in moderate and severe CFS/ME
September 17, 2015
11 Comments
New Australian study shows immune difference in moderate and severe patients. It may lead to a test based on these markers.