Welcome

The Lymphangiomatosis & Gorham's Disease Alliance is a 501(c)(3) nonprofit foundation dedicated to patient support, advocacy, and research to find effective treatments and cures for those affected by the rare lymphatic malformations known as lymphangiomatosis and Gorham's disease. Thank you for visiting our website. Our goal is to provide relevant and useful information to help you become more knowledgeable about these diseases.

If there is a particular subject you are trying to find information about, and you cannot find it, please send us an email and we will do our best to help. Our email address is
info@lgdalliance.org.

News and Announcements

8/08/2008
Lymphatic Research Foundation Appoints First-Ever Executive Director
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4/28/2008
Lymphangiomatosis & Gorham's Disease Alliance receives IRS Department of Treasury Certification Letter for 501 (c)(3) status
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4/28/2008
First-ever Advances in Rare Bone Diseases Conference organized by Rare Bone Disease Patient Network/US Bone and Joint Decade
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12/18/2007
Lymphangiomatosis & Gorham's Disease Alliance Welcomes Three New Board Members
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12/18/2007
Lymphangiomatosis & Gorham's Disease Alliance Joins Rare Bone Disease Patient Network
Full Story

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Feature Marcus Veng Petersen Honoring...