Lymphangioleiomyomatosis (LAM)

This page has been archived. It has not been updated since 25/08/2011. External links and references may no longer work.

UK sources of information and / or support

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LAM Action

The site contains information which may be useful for patients with lymphangioleiomyomatosis or doctors caring for patients with LAM.

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Lymphangioleiomyomatosis (LAM)

Information from the British Lung Foundation.



Further sources / more detailed information

Some non-UK sites

The following list popular non-UK health information sites with content aimed at the general public. They are mainly from the US. They have not been checked to see if information about the above topic is included but these large sites are comprehensive.

More detailed medical information

The following list online sources of more detailed medical information, mainly from the UK. These sites are mainly aimed at health professionals, but are of interest to all. They have not been checked to see if information about the above topic is included, but information about most medical topics can usually be found.

Author:
Dr Tim Kenny
Document ID:
7545 (v3)
Last Checked:
25 August 2011

Disclaimer: This article is for information only and should not be used for the diagnosis or treatment of medical conditions. Patient Platform Limited has used all reasonable care in compiling the information but make no warranty as to its accuracy. Consult a doctor or other health care professional for diagnosis and treatment of medical conditions. For details see our conditions.