Using the internet to cope with chronic fatigue syndrome/myalgic encephalomyelitis in adolescence: a qualitative study (Brigden et al., 2018)

[Snowdrop]

I thought seeking help online was a big no-no for ME sufferers, they should be dissuaded from googling ME and joining online support groups at all costs?

Yes, does anybody have the citation and quote relating to this view that online communication encourages people to think they are sick?