Fatigue survey results from MS International Federation

Interesting survey results on fatigue and MS.


Pat x

Hi Pat,

Thanks for that. Interesting, although I’m not sure it tells us anything we didn’t know. Hmmm: “Most” MSers have fatigue, it can have a high impact, and it’s difficult to treat…

No surprises there!



Yes agree doen’t tell us anything we didn’t know… but I suppose these surveys are useful to inform others. Don’t suppose Atos (those people who do the benefit tests) will take any notice… but you never know. It all adds to the ‘knowledge pool’.

Pat x

Thanks for that Pat, it helped my wife understand me a bit better by letting her know this is ‘normal’ and not to be too worried.