Joeblow604
Established Member (Voting Rights)
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.
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.