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
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...
See You at our Annual Meeting, 7 June 2025!
LAM Action's 2025 annual meeting will be on Saturday, 7 June, at the Leonardo Hotel London Watford. We will hear about LAM Action's activities over the last year, get practical tips and advice about living with LAM and learn about ongoing research. The meeting is for anyone with LAM, as well as their family and friends. It offers a great way of...
London and Southeast LAM Get-together
The next get-together of the London and Southeast LAM group will be on Saturday, 22 March 2025. If you would like more information, please contact Jill Pateman
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.
