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 to info@lgdalliance.org and we will do our best to help.