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
Annual Meeting 11 June 2022
LAM Action's annual meeting will be held virtually on Saturday, 11 June 2022. We will kick-off with our formal AGM at 10 am, followed by what promises to be an extra special meeting of presentations and celebrations. This year marks LAM Action's 25th Anniversary, and our meeting will highlight the tremendous progress made in LAM research,...
Lavender Group (virtual) get-together
The next virtual get-together for the Lavender Group (those with LAM born before 1960) will be on Tuesday, 14 June, from 18:00 – 19:30 BST. Anyone who would like to participate in this online chat should contact Jill Pateman by Tuesday 7 June and she will send you the Zoom link.
2022 Spring Edition of LAMPost
The latest edition of LAMPost is filled with interesting reports and news. It has pieces on Joan Mensor - Clowning Around for LAM Action; the International Survey of COVID-19 in Women with LAM; the launch of the 25 Challenge for May and new trustee, Harriet Saunders . Download the style that suits you, to read on your phone LAMPost...
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.
