25% group

Ensuring the Voice of the Very Severely Affected Myalgic Encephalomyelitis/Chronic Fatigue Syndrome Patient Is Heard in Research—A Research Model 25% ME Group Abstract Most of the research about Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) has focused on ambulant patients who...

This thread has been renamed to include general discussion of pacing for people with severe ME/CFS as well as the leaflet linked in this first post. 25% ME Group pacing leaflet (among other things, it differentiates between CFS and ME) https://25megroup.org/download/1796/?v=3222 It ends: ---...

25% ME Group stance on exercise https://25megroup.org/25-me-group-stance-on-exercise https://25megroup.org/wp-content/uploads/2020/08/25-ME-Group-stance-on-exercise.pdf We are the 25% ME Group Charity, the only charity concerned specifically with the needs of those most severely affected by...

25% ME Group: 25 year anniversary of the 25% ME Group https://25megroup.org/25-year-anniversary-of-the-25-me-group by Simon Lawrence This year marks the 25 year anniversary of the 25% ME Group, the only charity concerned specifically with the needs of the severely affected. Further details –...

Download link, https://25megroup.org/download/2302/?v=2840

The 25% ME Group: The Crushing Physical Burden of ME by Simon Lawrence of the 25% ME Group for those with severe ME on 14/08/2018 https://25megroup.org/the-crushing-physical-burden-of-me There is clear evidence that ME is not the same as depression or any other psychiatric disorder. In 2015...

The 25% ME Group - for those with severe ME - has a newly designed website - https://25megroup.org/ From the page "What is severe M.E.?" - https://25megroup.org/me ME is a WHO classified neurological disease with multi-system dysfunction. It is a physical disease that in its more...