When travelling with Crohn’s Disease, the best thing you can do is be fully prepared before you go. Things such as travelling with extra medication, taking a doctor’s note, packing a medical kit, and calling the hotel in advance to make sure that there’s a fridge in the room to store liquid meds are SO important to do in advance. It’s bad to be caught off-guard as an able-bodied person, but with Crohn’s Disease, the risks are so much higher.
A couple months ago before the Coronavirus pandemic blew up, I went on a small trip around Europe. During that time, I thoroughly indulged myself in chocolate and cheese in Switzerland (note: I’m intolerant to dairy), along with partaking in other activities which usually cause gut irritation (constantly travelling, having no sleep, etc). When I finally landed in Cologne, my stomach was in turmoil – and I ended up spending the whole trip trying to get back to my former self.
In Crohn’s Disease, a flare-up is a sudden reactivation of symptoms where inflammation becomes more present in the body – and by my own carelessness and gluttonous nature, I had provoked it into returning. I had several weeks to really focus on bringing that inflammation down, and after just a few days, my stomach had returned to normal (or at least, as normal as it can be for someone with Crohn’s).
This is how I did it.
TOOK IT EASY
My travel partner and I became the queens of slow travel once we’d finally landed in Cologne. Aware of the fact that we hadn’t relaxed properly in about a week, we took our time visiting museums and bookstores, and interspersed each visit with long stunts of cafes and rest. We took everything real slow and were careful not to overdo it – after such a hard couple of weeks on my stomach, it was beneficial to just take some time out to really listen to my body.
SWITCHED DIETS
After the dairy overload in Switzerland, I decided to switch to a diet that would be kind to my digestive system. I cut out food groups that are known to cause inflammation, and introduced more gut-friendly foods. My diet was low-fibre, but I still made sure that I was getting at least the recommended amount of vitamins. In times of flare ups, it’s hard to make sure that you’re not bordering on malnutrition, so it’s even more important than usual to keep re-introducing the good stuff to your body.
MADE MYSELF COMFORTABLE
Instead of bunking down in a stressful little hostel, we stayed in a private room in the gorgeous Koncept Hotel. This directly contributed to making sure that I got enough sleep each night, so that I would give my body a chance to heal during REM. Staying somewhere comfortable and avoiding stress is a key thing to keeping inflammation down, slowly helping to draw myself out of the flare up. Another key thing is to not stay sedentary – so little strolls and spending time dedicated to moving about is just as important as slowing down and taking it easy.
TOOK EXTRA MEDICATION
Luckily, I always pack more medication than I should need for this very reason. Not only does it cover my bases in case I lose a bag at the airport, but it also means that I can double-dose my medication when I feel like I need it most. Depending on the type of medication you take, this may not always be possible – but it’s worth checking with your doctor beforehand to see if you can double the dosage or incorporate another drug into your diet, should you desperately need it.
WATCHED WHAT I DRANK
Throughout the whole trip, I made sure to avoid alcohol (especially the much-loved German bier!), as the carbonation and acid would irritate my digestive system and contribute even further to the level of inflammation of the stomach lining. I also avoided fizzy drinks (due to the sugar and carbonation) and anything heavily caffeinated, instead sticking solely to water and green tea.
STAYED HYDRATED
Making sure to stay hydrated with bottled water and calming teas such as jasmine and camomile, I was able to both make up for the liquids I was losing, along with helping move on the toxins forming in my body and keep my digestive tract clear and ready to heal. It’s one of the most basic things to do when you’re a sufferer of IBD, and yet its importance is often overlooked.
BOOKED A DOCTOR’S APPOINTMENT
Whilst it didn’t seem necessary to book an appointment in Germany for the short time that I was there, I still made sure that I would have an appointment waiting for me back home. Doing this meant that I was prepared with what to do next, making sure that I could bring myself back up to top health as quickly as possible
Crohn’s Disease is an auto-immune disease affecting every part of the body – from the stomach, to the joints, to the skin, to the eyes. Unfortunately, I seem to have every little side-effect relating to Crohn’s, which can make it quite an overwhelming illness at times. However, when my dream is to become an explorer, I really can’t let a little thing such as having an incurable disease stop me. Some things are simply more important.
If this has educated y’all a little more about what it’s like to travel with Crohn’s or has helped you in any way, let me know in the comments below!
It’s good to know about Crohn disease, I honestly didn’t know about it. I like the idea of slow down kind of holiday, when I travel with my boys this is actually how we do our holiday. It’s not only less stressful but you can enjoy more the lifestyle of the city.
I completely understand about having extra medicine on hand. Sometimes you just never know! I had very bad asthma so I always have to take extra precaution when I travel, especially if I’m not sure I’ll be able to get the medicine I need where I’m going!
I’m glad you got it under control. Definitely sounds like you were prepared.
Wow impressed that you are finding a way to travel in spite of having Crohns….I know that can’t be easy! But sounds like with a little preparation, it’s definitely possible. I’m happy your sharing your story and giving hope to those going thru the same thing! <3
I’m glad to know you were able to manage throughout your trip even though your crohns showed up. I think it helped that you decided to take your trip slow and easy. 🙂
Always stay safe, Amy! 🙂
I’m sorry to hear you had a flare up whilst travelling, it must have been annoying that you were not completely comfortable. I hope you managed to make the most of the trip anyway, at least you stayed in a super fancy hotel 🙂 xo
This had to be difficult, but I know that your article will help many others! Thanks for having the courage to share!
Thank you for sharing, I don’t know much about Crohn’s except a friend of mine had it and every time I have seen her (at work) she would say I know I am not supposed to eat this but I am anyway, so I was never really sure what she could eat. I’m sorry to hear about your flare-up, but it sounds like you were prepared at least.
This is a great guide! My bro has recently been diagnosed with Crohn’s so I’ll be forwarding this article onto him.
I’m so glad you found a way to fully enjoy your trip! It would be killing me if I wouldn’t be able to try all the crazy stuff you can find while traveling since I’m a big food lover, but on the other hand, I’m sure that gives you chance to enjoy in many other things 🙂
Never heard of this illness before, so thanks for the introduction. Sounds like you were well prepared and that is always good. I can’t wait to travel.
Ugh I hear you. I have something called SIBO which is similar. It caused by lack of motility of the intestines, in my case from adhesions which is a form of scar tissue that adheres to all the organs and is an allergic reaction to the gas that they pump in the abdominal cavity to separate the organs. It is somewhat less intense then Crohns. The downside is there are no flareups. It is on 24/7 365 and you react to all food as it is the process itself that is the problem. So yes I know not easy to live with at all.
Allie x
I think this kind of posts are really useful to share for people that need this tips well traveling and make it more easy.
I hope you keep well,
Kisses,
E
My sister and I both have varying degrees of an auto-immune disease. Mine can mainly be managed through diet but hers is much harder to manage. I’m glad you know what your triggers are and how to manage them. Is it seasonal as well?
Planning ahead is a good thing to do with or without a disease, but especially with one. You did well and followed the rules you knew you needed to follow. Some folks never quite figure that out.
Have a fabulous day and rest of the week. Stay well. ♥
I have a friend that has this and it can be tough sometimes, but it does help to be prepared and to know your triggers!
Carrie
I love reading your stories! I’m glad that you were able to get back in control, and are now back to being as healthy as you can be. I can really see why Crohns can impact every little thing you do.
Stay safe! 🙂
xoxo
Lovely
You were prepared perfectly, I think this is so important. Loved to read your tips, I’ve never heard of Crohn’s disease. Now I learnt something about it.
xx Simone
Wow. Thank you for sharing! I’m sure this post will help many others. I’m very impressed you are aware with what triggers your flare up. I hope you are doing well and stay safe!
My aunt had Crohn’s disease so I know how serious it can be. Glad you took care of yourself during this trip. Be safe my friend!