We’re a family that loves to explore. Whether we’re wandering the colorful streets of Croatia, zip lining in the the Alps or tracking down the best gelato in the Netherlands, travel has become one of our favorite ways to learn, connect, and make memories together.

Of course, traveling with cystic fibrosis in the mix means we pack a little differently than most. Along with clothes and toiletries, we lug around an extra suitcase full of daily and emergency meds, Matthew’s vest machine, two nebulizers (in case one breaks!) and plenty of feeding tube supplies. And let’s be honest: sometimes things go sideways. We’ve had to replace a nebulizer in Austria, refill a critical prescription in Germany (after realizing it had been left behind), and figure out how to keep meds cold in a hotel room that didn’t have a fridge. But somehow, even the logistical hiccups become part of the adventure.

We believe that travel should be possible—and joyful—even when it takes a little extra effort. For us, it’s about saying yes to experiences, even if they come with a carry-on full of medical supplies. It’s about showing Matthew the world, and showing the world what’s possible with CF.

Click on any photo below to visit that country’s gallery and see where the road has taken us so far. Thanks for coming along for the ride!