Living with tracheobronchomalacia (TBM) can be challenging, not just for those who have it but also for their loved ones. When family members don’t understand what TBM is, it can lead to confusion, worry, or even frustration. I’ve found that breaking down the condition into simple ideas helps everyone feel more connected and supportive. Here, I want to share some easy ways to explain TBM to family, so they can better understand what you or your loved one is going through. C

When I first heard the term tracheobronchomalacia (TBM) , I was overwhelmed. It sounded complicated, almost like a foreign language. But as I learned more, I realized that explaining TBM to my family didn’t have to be confusing or scary. It’s about breaking down the medical jargon into simple, relatable ideas. If you’re trying to do the same, you’re in the right place. I want to share what I’ve learned and how I’ve approached this delicate conversation with honesty and clarit

Living with tracheobronchomalacia (TBM) is a journey filled with uncertainty, challenges, and hope. When I first encountered this condition, I felt overwhelmed and isolated. I dreamed of a community and a cause that gave me purpose: CureTBM. If you’re wondering how to get involved and make a difference, I’m here to share what I’ve learned along the way. This guide is about more than just joining an organization—it’s about becoming part of a movement that can change lives. Why

I still vividly recall the first time I realized something was terribly wrong. It was Easter Sunday, just weeks after I had completed one of New England’s toughest mountaineering challenges—summiting all 48 4,000-footers during a single calendar winter. A Moment of Realization I had never been fitter—or so I thought. It was meant to be an easy pre-meal hike with my young teen and my mountain climbing bunny. But shortly before the final push to the summit, I noticed my son was