- About LAM
- About LAM Action
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The 2015 Annual Patient Meeting will take place on Saturday June 6th - put it in your diaries now!
LAM patients making their way home from the annual meeting
LAM Action is the UK charity for patients with Lymphangioleiomyomatosis (LAM), their families and doctors caring for them.
LAM is a rare lung disease that occurs only in women. For every million women approximately 7 will have LAM. We are aware of approximately 200 women in the United Kingdom who have LAM and around 10 new cases are diagnosed each year. It appears to occur worldwide and to be equally rare in other countries.
LAM predominantly affects the lungs, where it causes excessive growth of smooth muscle cells which progressively destroy lung tissue and erode lung function. Although research is ongoing, currently there is no cure for LAM and little effective treatment. For some patients lung transplantation is their only means of survival.