why is it still so poorly understood?

[Theresa60]

Very powerful article that asks some very important questions about the medical politics surrounding myalgic encephalomyelitis.

opendemocracy.net/naomi-whi...

[Bellated]

It wasn't until I needed help with my health that I realised there was no safety net and self management with advice from fellow sufferers was normality.

[ukmsmi4]

This excellent article only touches on the politics of the neglect of ME over decades. The truth behind it gets even more disturbing when you dig deeper into it.

One day the truth will out. Not just about the illness itself but the empire building and career protecting that has gone on over decades whilst leaving thousands of people alone and in the dark in huge amounts of physical, mental and emotional pain.

Let's hope the psychobabble brigade will be made to hang their heads in shame.

[Ian123]

The murky politics of psychiatry jcoynester.wordpress.com/ are involved heavily in the incestous promotion of an artificial construct CFS by a clique that have careers invested in retaining control of the narative on this neuroimmune condition.

[CheshireKatz]

Truly heartbreaking account of state sponsored child abuse brought tears to my eyes.

[readerlist]

Norway a country whose government have apologised for previously bad treatment of patients move on with groundbreaking research.

kavlifondet.no/2016/12/new-...