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
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...
LAM and Mental Health Long Term
Consultant clinical psychologist Dr Victoria Hill looks at the long term mental health issues that may arise from a LAM diagnosis and suggests some strategies to cope with them. This is the second of two talks, produced by LAM Action, that contain input from and aim to support the LAM community in the UK. ...
LAM Action Virtual Meeting celebrates 25 years
LAM Action celebrated 25 years with a really positive virtual meeting on 11th June 2022. The 3 hour event included a history of LAM from Prof Anne Tattersfield OBE, research updates from Prof Simon Johnson and Dr Debbie Clements, a tour of the Nottingham research lab, messages from LAM Groups around the world and the Lucy Falconer Talk was...
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.
