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Traveling with CF: Do you have any summer plans?
Hope everyone had a great weekend!
With the summer approaching, many people have trips and vacations planned. Anyone in the CF community knows that traveling comes with additional modifications and adaptations. Whether you are a patient or a caregiver, traveling with CF requires more preparation than it does for other people.
Do you have any summer travel plans? What tips and tricks do you have for traveling? What are some favorite trips that you’ve taken?
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4 Replies
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Travel writer who lives with CF here! I take 7+ trips a year (most of them international) and have to do a lot of prep work to make it happen. The hardest part is packing all of my medications, and I always bring a lot of backups just in case something happens with my luggage. I make sure to schedule CF appointments in advance so I can check in with my doctors in between trips, and once I’m in a destination I give myself a few days to adjust and get back in a healthy routine. Always happy to talk about traveling with CF if anyone has questions!
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That’s awesome! Yeah, it’s definitely a lot of things to prep for. What is your next trip planned?
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I’m traveling right now, actually! Six weeks in Ireland, Italy, and Peru.
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How fun! Stay safe and let us know how the rest of your trip goes! <3
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