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
New LAM Action Christmas cards are available
Thinking of ordering your Christmas cards? LAM Action has the solution. The new range of LAM Action cards is here. There are 5 designs to choose from: Floral Hare, Christmas Story, Winter Birds, Christmas Cafe and Golden Christmas Tree. Use the form below if you would like to order. xmas card order form 2022
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...
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.
