Has anyone else watched these new documentaries about living with ME/CFS? I watched Unrest yesterday; it was hard to watch the suffering of those involved ... I could relate only too well to their pain. Yet I feel the films will be fabulous tools for raising the awareness of the general public as well as family, friends etc. Hopefully doctors? Hopefully funding bodies? I urge everyone on this ProHealth board to share the films on FaceBook, tweet, discuss, share, blogs etc in any way possible to help raise awareness of our illness. Our suffering has been invisible for too long!