LAM Action provides valuable support to those with LAM and their families and helps fund important research into LAM. It is a small charity focused on an extremely rare disease, run almost exclusively by volunteers which generates almost all of its income from donations and fundraising. 

Lymphangioleiomyomatosis, known as LAM (as it's a bit of a mouthful), is a very rare disease that affects women almost exclusively. It is characterised by lunch cysts, abnormalities in the lymphatic system, and non-malignant kidney tumours. 

The charity is very small, and so a little goes such a long way in providing support to women with LAM and research to find a cure. 

Thanks to you all for the support and any help is greatly appreciated.