Collinson Foundation for Patulous Eustachian Tube
From Echoes to Action
Be part of the movement to raise awareness and improve the lives of those affected by Patulous Eustachian Tube Dysfunction (pETD). Whether you’re a patient, caregiver, medical professional, or advocate, your support drives education, research, and community outreach. Together, we can make a difference.
Who We Are
The Collinson Foundation for Patulous Eustachian Tube Dysfunction is a nonprofit dedicated to raising awareness, advancing research, and supporting those affected by PET, a rare and often misunderstood ear condition. Founded in memory of Craig Collinson, who struggled for years to find effective treatment and support while living with PET. The daily challenges of the condition took a profound toll on his quality of life and mental health. Craig died in March 2025. In sharing his story, our mission is to provide reliable information, connect patients with resources, and advocate for better diagnosis, treatment, and support.
The first book dedicated to helping those with pETD
Written by CFPET Co-Founder Emily, this book takes you through her personal journey with this condition. Filled with resources from treatment options to doctors, this is a must-have for anyone struggling with, or who has a loved one with pETD.
A portion of all proceeds are donated to CFPET.
“We need to ensure pETD is included as a disability, find funding for research, come together in bombarding ENTs with knowledge, etc”
— Vickie Kropinski Imms, mother of a pETD sufferer
