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
Winter LAMPost – out now
The 2021 Winter edition of LAMPost is filled with interesting articles and updates. It has pieces on getting fit for the New Year, Fundraising events for you and your friends and the story of Sally and Ron's Christmas tree field. Download the style that suits you, to read on your phone LAMPost Winter 2021 Mobile Device Friendly or to print...
South-West Group (Virtual) get-together
The next virtual get-together for women with LAM in the South-West will be Thursday 27 January 2022. Anyone who wants to participate in this online chat should email Jill Pateman no later than Tuesday 25 January.
Green Group (Virtual) Meeting
The next meeting of the Green Group (for people with LAM born in 1980 or later) will take place via Zoom on Monday 10 January 2022, between 6-7:30 pm. If you'd like to join the online chat, please email our LAM Action coordinator, Jill Pateman, no later than Tuesday 4 January and Jill will send you a Zoom link.
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.
