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
Jade Group Meeting
The next meeting of the Jade Group (for people with LAM born between 1960 and 1980) will be Monday 29 November 2021. Anyone who wants to participate in this online chat should email Jill Pateman no later than Tuesday 23 November.
LAMPost Summer 2021 edition
Our LAMPost Summer 2021 edition is out now. You can download a print-friendly or mobile device-friendly version.
LAM Action News
The theme of repurposing medicines for use with other diseases was recently discussed at the LAM Action Annual Meeting. Medical research charity LifeArc, and law firm Pinsent Masons have published the key lessons from a March 2021 seminar aimed at supporting charities, researchers and funders researching new uses for existing medicines. LAM...
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.
