- About LAM
- About LAM Action
- For Medical Professionals
- For Patients & Their Families
- Get Involved
With less than a month to go before the last posting dates for Christmas we currently have 25% of stock left - so please hurry and place your order!
The 2015 Annual Meeting will take place on Saturday June 6th in Nottingham. Click here to see some FAQs
The LAM Action Annual Meeting is a great way to meet other women with LAM, and get all the info. you need
Some of our members making their way home from the annual meeting
LAM Action is the UK charity for those with Lymphangioleiomyomatosis (LAM), their families and doctors caring for them.
LAM is a rare lung disease that occurs almost exclusively 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 effective treatment is limited. For some women with LAM lung transplantation is their only means of survival.