As you can see from my ticker, there's 111 days til my trip. Without boring EVERYONE with specifics, i have suffered from ME/CFS for almost 6 years now.
Is there anyone else here that is going, or has been to WDW with this illness?
I would have posted this on the Disabilities forum, but i especially interested in it from a UK point of view with the long flights and time difference.
I understand if others don't want to share specifics on a public board, but if you have some tips or advice, i'd be very grateful if you could PM me!
I'm interested in finding out how you coped with the long flights, the time difference, alterations to sleeping patterns, how much you could do at the parks, if there's anything special you couldn't do, and most importantly; given the illness and your experience, would you do it all over again!
Thanks,

Is there anyone else here that is going, or has been to WDW with this illness?
I would have posted this on the Disabilities forum, but i especially interested in it from a UK point of view with the long flights and time difference.
I understand if others don't want to share specifics on a public board, but if you have some tips or advice, i'd be very grateful if you could PM me!
I'm interested in finding out how you coped with the long flights, the time difference, alterations to sleeping patterns, how much you could do at the parks, if there's anything special you couldn't do, and most importantly; given the illness and your experience, would you do it all over again!
Thanks,
