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When I decided to study abroad in 1974, I also decided that I would not allow CF to stop me from living my life to the fullest.

If you have cystic fibrosis-related diabetes (CFRD), the following are some tips to help you manage your treatment while traveling. 

Check in with your cystic fibrosis care team several months before your trip.

Going on vacation without your child with cystic fibrosis can be hard, but here are some tips to help make it a little easier.

My experience traveling with cystic fibrosis has taught me that a chronic illness should never slow you down. It may require extra planning and packing, but it’s worth it and definitely doable.

With the holidays fast approaching, it's time to prepare for the change of schedule in your cystic fibrosis routine.

During my five months in Denmark for a study abroad program, I not only learned more about myself and others, but I became more confident in my ability to take care of myself. Don't let CF stand in the way of experiencing that, or any other dreams.

Thinking of how you will take care of your health while traveling with CF can be very intimidating. For 28-year-old Stacy Motenko, preparation is the key.

After what seems like an hour and too many clicks to count, you finally did it. You booked your flight! A couple weeks leading up to your departure date, panic starts to set in. You go into operation “no one better get me sick” mode.

Hear how frequent flier Stacy Motenko keeps herself organized as she turns traveling with CF into a manageable affair.