Having read more about the disingenuous and manipulative way that some believe CFS patients should be treated, in order to 'build a collaborative relationship' or whatever, I'm deeply sceptical of anyone making money from CFS in the NHS. Until there have been pretty radical changes, and a lot of quacks fired, I want to stay as far away from any 'fatigue clinic' as is possible.
I think that patients should be spoken to as honestly and clearly as possible, and do not want to play a part in any system which does not recognise the importance of this.
edit: Also though, this is very much my personal choice. ~Other people have different values and preferences, and unfortunately, there are pretty limited options available to people with CFS. I would say that it's worth remembering that those making money from CFS who are not (for example) also calling for the release of the PACE trial's protocol defined outcome measures have made moral decisions about how patients deserve to be treated, and this should affect how you view their 'caring' toward you.