I’m writing this on a plane, on my way home from visiting family. A lot of my relatives live on the east coast and it was a yearly trip when I was younger. This was the first time I’d been out for about 5 years and it was a great chance to see relatives and re-live childhood memories!
I’ve travelled a lot in the past 10 years or so, including teaching overseas, and travelling from there. I’m determined to not let MS stop me from experiencing the world. I’ve travelled even when I was out of remission at times, but for some reason it was a more difficult trip to pack for and plan this time.
Things have changed a bit, so when I packed to leave I had a suitcase almost full entirely of medical needs, including a large amount of food as MS related digestive issues are becoming very problematic, but can be managed by eating carefully. I also had quite a few “just in case” items like my cane. Complicating things further was that I drove with my parents one way and flew home, so that left me trying to plan and pack and re-pack for different requirements.
But the real point is that it was possible, although requiring a lot of planning, lists, re-packing and thinking through things I made it, I was there to see family, I waded in the ocean (even though the cold water hurt), I had some seafood and most of all was able to participate in a family vacation, and I lived to tell the tale!
I hope whatever you are doing this summer you are enjoying it! Happy Trails to all those travelling!