How do you cope on Holiday with ME/CFS
Posted , 7 users are following.
Hi,
Just wondered how other people cope with the family holiday. Being out of your normal routines and in a new place perhaps. What do you put in place to help you cope?
Being at home knackered is one thing but being in a caravan, apartment or hotel etc. is much different. Having to be mobile and do holiday stuff with the kids, can and is an overload for my system. Do you avoid going away because of things like this or is it just me?
The last 10-day holiday we took has taken me 4 months to get over! (Moreover, I was still feeling rough after 4 months…) I know I am lucky to be able to grab a family holiday, but I do wonder at times, if it’s more harm than good taking a holiday with ME/CFS.
1 like, 34 replies
JulieBadger dragontest
Posted
This year we are having a week in a caravan 35mins away ish. We will also be taking my car cos my car the seating position is more like a dining chair rather than hubby's which is lower with legs more out front.
We also own a sea-side chalet which is 30mins away. We go for weekends and a week at Easter there. That's nice with proper sofas and beds. x
dragontest JulieBadger
Posted
Glad to hear you are managing to get a break from the house. i have been just 10 miles away in a caravan in a "basic" field and had a great time, like you it was a change for struggling with stairs. I struggle with the travel inns type of places as you need to be out of the room for the cleaners etc, thats when we tend to go somewhere and I overdo it :-(
GeorgiaS dragontest
Posted
JulieBadger dragontest
Posted