I think the posts earlier in this thread about the comments that this service made about the draft NICE ME/CFS guidelines in 2021 remain relevant. From looking at the video above, I don't think the views or attitudes of the Newcastle services have changed. Indeed, the approach seems to ignore (ME)/CFS as much as possible and just talk about and treat 'fatigue' in an extraordinarily patronising way.
I wish there was a way to protect children with ME/CFS from the ministrations of this service. Instead, it now seems that the service's 'expertise' is being shared with other BACME clinicians.
I wish there was a way to protect children with ME/CFS from the ministrations of this service. Instead, it now seems that the service's 'expertise' is being shared with other BACME clinicians.