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
Summer 2022 LAMPost
The summer edition of LAMPost is now available to download, with lots of articles and info that you won’t want to miss! Download the style that suits you, to read on your phone: LAMPost Summer 2022 Mobile Device Friendly or to print: LAMPost Summer 2022 Print Version
London/SE LAM Group In-Person Meeting
For the first time in over two years, the London/SE LAM Group will be meeting in person! Our get-together will be on Saturday, 24 September, from 2:00 pm. We are scouting for a location convenient to a Central London train/tube station and hope to find something with outdoor seating (and hope for suitable weather too!). If you would like to join...
Harriet’s story
Harriet has only recently discovered that she has LAM and talks frankly about the experiences that led up to her diagnosis and how a visit to a LAM Action meeting helped her to come to terms with the disease.
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.
