A community-led 501(c)3 non-profit working to improve the lives of those with complex lymphatic anomalies: GLA/lymphangiomatosis, Gorham-Stout Disease (GSD), Kaposiform lymphangiomatosis (KLA) and central conducting lymphatic anomaly (CCLA).
We serve people affected by CLA through programs of research, education, and advocacy by
• Providing up-to-date resources and a support network for patients and families
• Working to build a clinical network for patients of all ages
• Guiding and funding research by doctors and scientists
• Powering the LGDA Patient Registry, an IRB-approved study
We invite you to contact support@lgdalliance.org for more information about how your donation helps.
A community-led 501(c)3 non-profit working to improve the lives of those with complex lymphatic anomalies: GLA/lymphangiomatosis, Gorham-Stout Disease (GSD), Kaposiform lymphangiomatosis (KLA) and central conducting lymphatic anomaly (CCLA).
We serve people affected by CLA through programs of research, education, and advocacy by
• Providing up-to-date resources and a support network for patients and families
• Working to build a clinical network for patients of all ages
• Guiding and funding research by doctors and scientists
• Powering the LGDA Patient Registry, an IRB-approved study
We invite you to contact support@lgdalliance.org for more information about how your donation helps.