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.
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Going on vacation without your child with cystic fibrosis can be hard, but here are some tips to help make it a little easier.
With a record 45 clinical trials either ongoing or starting up in 2016, research coordinators and principal investigators throughout the Therapeutics Development Network took time out in San Antonio recently to discuss clinical research and put attendees through boot camp.
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.
Dr. Skach discusses the latest advances in CF research and exciting new approaches to address the underlying cause of the disease.
During our family round trip from Oklahoma to Florida, I learned a thing or two about traveling with a CF tot.
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.
Hear from John P. Clancy, M.D., the first plenary speaker at this year's NACFC, about recent advances in personalized medicine, which could allow clinicians to better tailor treatment to the individual with CF.
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.