We’ve already seen what happens when the LAM community comes together. We listen. We learn. We speak up. And then we turn what we’ve learned

I don’t like being told “no.”  When it comes to living with Lymphangioleiomyomatosis (LAM), I research, adapt, and advocate not only for myself, but for the thousands of women

We are excited to share a peek at progress from a promising Foundation funded study led by Dr. Roya Babaei Jadidi at the University of

The LAM Foundation is proud to celebrate the publication of new research from Mary Beth Brown, PT, PhD, and her collaborators, including Dr. Claire Child, at the University of Washington.

For more than 25 years, Dr. Marina Holz has been asking questions, exploring ideas, and looking for answers as a scientist. For the past 15 years, she

Bonnie Wang, MD, is a Clinical Associate Professor in the Division of Pulmonary and Critical Care at the University of Michigan. For the past seven

When Kat was diagnosed with LAM nearly 13 years ago, shortly after the birth of her first daughter, she didn’t know what the future would

For many people living with LAM, a visit to the National Institutes of Health (NIH) can bring a mix of emotions. You may feel hopeful

What you Need to Know: Every once in a while, an opportunity comes along that allows our entire community to make a real difference with

Efforts include support for earlier diagnosis through LAMair™, TrilliumBiO’s newly developed VEGF-D test Rockville, Maryland and Cincinnati, Ohio — June 29, 2026 — TrilliumBiO, a

The LAM community has always understood something powerful: the people living with this disease are essential partners in advancing research. Today, we are proud to

Dr. Daniel F. Dilling has spent his career helping people with rare lung disease feel seen, supported, and cared for. He is a highly trained