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What are your CF traveling tips?
Traveling in general is a headache; traveling with cystic fibrosis can cause a migraine. While others can pack just the essentials, those with CF need their meds, backup meds, a vest, a vest machine, and to know where a CF-proficient hospital is in the area they are going to. It’s very daunting, but it can and is done!
As a kid, my mom took packing for our trips very seriously, knowing that if we forgot a medication, I would not feel well. We used a pill organizer and pill charts. We also allotted extra time for the TSA to scan my vest, machine, and meds.
Share how you make traveling with CF less of a migraine! Any creative ideas that others just HAVE to know?
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