WebI know there is different degrees/ severities of CFS and I have a hard time to understand what "the less severe" CFS does look/ feel like since every documentary, interview, article etc I've watched online or read sofar they seem to show the rather severe cases where people suffering from it basically are bedbound 24/7. Hi all, basically title. Web5 • take time to build supportive, trusting and empathetic relationships 6 • use a person-centred approach to assess people's needs 7 • involve family members and carers (as appropriate) in discussions and 8 care planning if the person with ME/CFS chooses to include them. 9 1.1.4 Recognise that people with ME/CFS need:
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