ME affects one in 500 people in the UK, but NHS services for ME patients are below par and research funding is negligible compared to other chronic conditions.

How the one-size-fits-all benefit system is failing to assess the complex and sometimes fluctuating symptoms of a brain injury.

Seeking help for such a secretive disorder, is like killing away your only friend, but with the lack of funding, is help really effective?

We speak to one sufferer about the long-term impact of being diagnosed with this life-changing condition.