It sure does take a lot of work to pack for a plane trip vs. a road trip. We had to check the regulations because they seem to change every 3-6 months as we get more and more removed from 9/11, yet constantly reminded with scares and dry runs that keep getting more regulations in place.

I got a letter from my CF doctor stating that I have cystic fibrosis and will be traveling with [several medications including these listed, but not limited to] and invited them to contact him directly if they have any concerns about what I’m traveling with. That brought a certain special peace of mind, considering that we have over $30,000 worth of medicine and equipment. Each dose of some of my meds is over $30 and my Vest was over $11,000. They will not be leaving our possession, that’s for sure.

To give normal folks and those with various milder forms of CF, here is what we’ve packed:
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