On a recent Breathe In podcast episode, Lea and I discussed some of our experiences with clinical drug studies. I’ve done a few throughout the years, some achieving their goals and others ending in failure. Since the episode aired I’ve gotten a few questions about the up’s and down’s of enrolling in clinical studies. For...
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If you’re living with cystic fibrosis, your life, to an extent, revolves around treatments. For 2+ hours a day, everyday, we’re doing treatments. Some of us can breeze through our treatments if our CF hasn’t progressed, while the rest of us feel like we’re getting a good workout in with each session from all the...
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It’s December so that means Christmastime is here! This year I’ve recruited some help for my gift list. The very lovely Salty Cysters themselves, Tiffany and Lea, have certified this year’s list suitable for people living with cystic fibrosis! 1. Salty Cysters Sweatshirt Lea: This sweatshirt is so cute & comfy. Who doesn’t love cozy sweatshirts...
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