Find out more about LAM
Learn more about lymphangioleiomyomatosis. We give an overview of LAM, its symptoms and how it is diagnosed and treated.
Find out what help is available
As someone new to LAM, you have probably never known anyone with LAM or even heard of this rare disease. One of our primary aims is to provide support and information to those with LAM and their families.
Recent NEWS
Spring 2025 LAMPost
The spring edition of LAMPost is now available to download - big thanks to all who contributed! Download the style that suits you, to read on your phone: LAMPost Spring 2025 Mobile Device Friendly Or to print: LAMPost Spring 2025 Print Version Happy reading and best wishes for Easter from LAM Action.
Patient Engagement
The unique patient engagement at the heart of the LifeArc Rare Respiratory Disease (RRD) Centre is discussed in a press release issued on behalf of LAM Action. To read a copy of the press release, please click here.
LifeArc Centre for Rare Respiratory Diseases
As part of the LifeArc research initiative Prof. Simon Johnson’s team and LAM Action are involved in one of four LifeArc Translational Centres for Rare Diseases: the LifeArc Centre for Rare Respiratory Diseases. Here's a fascinating video that explains how the LifeArc Centres...
GET INVOLVED
How can you help us?
LAM Action is entirely self-supporting and run almost entirely by volunteers. In this section you will learn about the many ways in which you can get involved.
