09/04/2026
I’m looking forward to guest speaking with three bronchiectasis support groups this month: San Francisco, the Las Vegas area, and, at the end of the month, Washington, DC and surrounding states.
Of course, airway clearance is always a favorite topic, but I’m finding that travel is quickly climbing the ranks! And really, so much of what people want to talk about boils down to one thing:
How can we put systems in place that make managing bronchiectasis a little easier, and give us more time to do what we really love doing?
Because bronchiectasis already asks a lot of us. Airway clearance, nebulizing, sterilizing equipment, medications, appointments, exercise, nutrition…the list can get pretty long.
Anything we can do to simplify the day-to-day management of our disease gives us a little more time and energy for the rest of our lives.
As I prepare for these talks, I’d love to hear what’s working for you.
Here’s one of my little systems. I’ve owned MANY pill organizers over the years, but living in a 900-square-foot apartment, I never loved having a big pill organizer sitting on my dining room table.
I like my home to feel happy and creative, and when I’m not using something related to bronchiectasis, I prefer to tuck it away in a cabinet. It’s not that I’m ashamed of my disease. I just don’t want it taking center stage in my home.
That’s why I love this organizer. I simply pull out one tiny little pill case for the day and tuck the rest away. Simple, neat, and one less thing to think about.
Now it’s your turn. What organizers, gadgets, routines, shortcuts, or systems make your life with bronchiectasis easier and give you more time for the things you love?
I’d love to borrow some of your best ideas for my upcoming talks!