Travelling with Crohn’s disease and ulcerative colitis can be challenging. Whether it’s working around medication access and schedules or dealing with flare ups and symptoms. But this shouldn't stop you from exploring new places.
Here are some travel tips to HELP get you started on your journey:
- Always travel with more medication than you think you’ll need. You never know when you might leave something behind on the airplane or a pill gets lost behind a dresser.
- Make sure to keep all prescriptions in their original container. This helps with any problems you may encounter at airport security.
- Always pack your medication in a carry-on bag. The last thing you need is to be without your daily medication because it’s halfway around the world in your checked-in luggage.
- Get back in touch with your inner toddler. Always try to use the washroom before you leave your hotel room or a restaurant. I find that the restaurant pit stop is the most important one because you know you’ve just eaten.
- Keep your eyes open for the universal washroom sign. Places like McDonalds and Starbucks are a great go-to stop as they are practically everywhere in the world and are guaranteed to have bathroom access. Also be aware of transit bathrooms—whether they are in the stations or on the planes, trains or buses you are boarding. (Some countries also charge a few cents to use public bathrooms, so try to keep some local coins on you at all times.)
- Listen to your body. If you know that certain foods cause you to need the bathroom right away, avoid eating them before long periods of travel where you’re unsure of bathroom locations.
- Most importantly though, when you are traveling with friends, family or people you’ve just met, always let them know about your health situation. We all have emergency, out-of-the-blue bathroom needs, and telling them about your disease will help keep the stress and nerves at bay when having to call for an unplanned bathroom break.
need more information?
Get into contact with your local chapter to hear from others about their experiences travelling with IBD and get helpful tips.
Contact firstname.lastname@example.org to receive more information.