The Province (Vancouver): Better treatment needed for 77,000 British Columbians with ME

Regarding the CCDP information @Sly Saint posted, it doesn't look like things will be turning around there after all. I was hoping the new director would change this up for the better. When I went there before they were promoting ME was a Central Sensitivity Syndrome. You did see a doctor once and all he did was review your psychosocial assessment and decide where you fit in program. IE speak to a ND, dietitian, CBT, etc. They did very minimal medical testing. Sounds like not much will change.

I remember getting frustrated with being told I am fatigued and not sick.

I have no idea where they get this from - "This group education format is supported by client feedback and research." Any time we've been allowed feedback its not what I see patients saying nor is it said in Canadian ME groups. The opposite actually.
 
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