Discussions
Discussions
Rin Check-In 01/20/2026
Hi everyone! We’re graduate students working on an academic research project for our graduate program at the University of California, San Diego, and we’re hoping to learn directly from this community.
Our goal is to better understand life with non–cystic fibrosis bronchiectasis, including current treatments and what the day-to-day experience is like from the patient perspective. If you’re living with non-CF bronchiectasis, we would truly appreciate you taking a few minutes to share your experience by completing a survey. We would also love to hear from any healthcare professionals in the group who care for people with this condition and are willing to share their perspective.
This survey is for educational purposes only, completely voluntary, and anonymous. There are no right or wrong answers — we’re simply interested in your honest thoughts and experiences.
Thank you so much for considering, and we’re very grateful for your time and willingness to help us learn from you!
Link to survey: https://docs.google.com/forms/d/e/1FAIpQLSc6Fpg17wPWVHa2f9C0fdGkN7_EAmO-7gzB7GQGNMcfy1UVaA/viewform?usp=dialog
Link to survey for health care professionals: https://docs.google.com/forms/d/e/1FAIpQLSf8lqN1OScc2F9Vz-_HjF5bUDF5umxQpFoP0uaNb6J6SjKbHQ/viewform?usp=header
It is not our intention to serve as a substitute for medical advice and any content posted should not be used for medical advice, diagnosis or treatment. We make every effort to support our members, our medical professionals cannot and will not provide a diagnosis or suggest a specific medication; those decisions should be left to your personal medical team. While we encourage individuals to share their personal experiences with COPD, please consult a physician before making changes to your own COPD management plan.
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