Originally posted 4 August 2018
Off on a 12 day trip to the US tomorrow for work. Pain has been pretty manageable lately, but I am a bit worried about a flare away from home, far away from any support. Especially since I’ve only had 2 big flares, so not sure how to deal with them yet. Any advice will be gratefully received.
Traveller’s tips
I did a lot of travelling in the early years of CRPS and very stubbornly did not look for any accommodations. Travelling is stressful, airport queues are long and the pressure in the aeroplane affects many people with CRPS. If you want to have a productive trip – get airport assistance!
One of the hardest things about CRPS is learning to deal with situations that aggravate your pain. You’re not “making a scene” if you need some help. Ask for help! Be kind to yourself.
