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New website signposts to information and support for women with LAM across the globe

New website signposts to information and support for women with LAM across the globe

We are delighted to launch our new LAM website, developed with the support of women with lymphangioleiomyomatosis (LAM) and healthcare experts working in the field, at the start of Worldwide LAM Awareness Month (June 2017).

LAM is a rare lung condition that mainly affects women. To find out more, download our factsheet (in 9 languages) and access our map of LAM patient support organisations on the in your language page.  

Find out what matters most to women diagnosed with LAM and read stories of the experiences of women diagnosed with this condition.

Please pass on details of the website through your networks to help spread awareness of this rare lung condition; and let us have your feedback.

We also want to acknowledge and thank the women of our LAM patient advisory group who helped guide the development of this project.

Visit the LAM patient priorities website

Visit the patient priorities homepage to see which websites will be coming next

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