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
£9.4 Million Research Centre for Rare Respiratory Diseases
For the first time ever, there will be a hub connecting people affected by rare respiratory diseases with a network of clinical experts, researchers, investors, and industry leaders across the UK.
See you at our Annual Meeting, 8 June!
LAM Action's Annual Meeting will be held in Birmingham on Saturday, 8 June, at the Macdonald Burlington Hotel. This is our first in-person meeting since 2019 and offers those with LAM and their families the chance to meet one another and hear about exciting research and other developments. We have a great programme with something for everyone and...
Spring 2024 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 2024 Mobile Device Friendly Or to print: LAMPost Spring 2024 Print Version Happy reading and best wishes from the LAMPost team!
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.
