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Category | L |
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Domain name | lamfoundation.org.uk |
The LAM Foundation urgently seeks safe and effective treatments, and ultimately a cure, for lymphangioleiomyomatosis (LAM) through advocacy and the funding of promising research. We are dedicated to serving the scientific, medical and patient communities by offering information, resources and a worldwide network of hope and support. Visit website
The LAM Foundation is a registered 501 (c)3 non-profit organization. All contributions are tax-deductible to the fullest extent of the law. If you have any questions about your gift, please call us at 513-777-6889 or email us at development@thelamfoundation.org. Join The LAM Foundation Community Ways To Give Help Raise Funds Speak Up Volunteer Visit website
LAM cells grow throughout the lungs, causing holes or cysts, blocking the airways and preventing the lungs from getting oxygen to the rest of the body. Sometimes, LAM cells also cause problems in the lymphatics and kidneys. There are 2 ways that you can get LAM: on its own – this is called sporadic LAM with a condition called tuberous sclerosis Visit website
01344 882717. Where next? View Our Prospectus. Entry to Lambrook. What Others Say. Come and see us. Come and see us. Dont take our word for it – come and see for yourself what makes Lambrook so special. Visiting the School. Contact Lambrook School Visit website