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/Southeast Support Group meeting
The next online meeting of the London/Southeast support group will be 25 October, from 19:00-20:00. If you are interested in attending, please contact Jill Pateman.
LAM and Mental Health Early Stages
Consultant clinical psychologist Dr Victoria Hill explores the mental health issues that may follow a LAM diagnosis. This is the first of two videos produced by LAM Action. The second proposes ways to live with LAM in the longer term.
Guide to PIP
The Personal Independence Payment (PIP) is a state benefit that might entitle people to financial help with daily living and mobility costs. People with LAM might need the benefit due to the effects of their LAM. We have published a flyer that describes PIP and the application process in more detail. To download a copy of the flyer, please click...
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.
