Nightsong
Senior Member (Voting Rights)
I'm not convinced that a "professional charity CEO" with no personal experience of ME/CFS is the right way to go. Many of them will want to move on eventually to bigger & better positions in the ever-burgeoning "third sector" that will be dependent upon the largesse of governments, large corporations & major charitable foundations. Seriously challenging the Government and the NHS, inevitably making enemies in the process, might well not be to their career advantage despite being what we desperately need.
(Even monies dedicated to research have been wasted on the Tyson project - which further enables & entrenches the psychobehavioural clinics, giving them the ability to say they are using "patient approved" tools & resources - as well as "dysautonomia protocols" by rehabilitationists & other such nonsense. And then there is the issue of fungibility.)
Absolutely not. Contributing to any organisation that is collaborating actively with BACME and supporting psychobehavioural clinics is contributing to the furtherance of ongoing harms.PeterW said:we need to get better at engaging our wider communities to raise money and donate to the ME Association, Action for ME and ME Research UK.
(Even monies dedicated to research have been wasted on the Tyson project - which further enables & entrenches the psychobehavioural clinics, giving them the ability to say they are using "patient approved" tools & resources - as well as "dysautonomia protocols" by rehabilitationists & other such nonsense. And then there is the issue of fungibility.)