Does your doctor and the french think CFS/ME is a mental disease like the UK or a physical(possibly infectious) disease like the US and canada? 100euros is cheap but i won't be traveling to paris for GET. How long were you disabled and suffering from CFS/ME before you got well? Do you think maybe everything you did was just coincidental and that you're one of the lucky ones who experience remission from CFS/ME? It's been said by many CFS specialists that those experiencing remission have a higher chance if they are younger and within the first 2 years of this horrible disease.