LGDA ensures patients with complex lymphatic anomalies (CLAs) have the comprehensive support they need from peer, medical, and scientific communities to lead longer, higher-quality lives.
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Patients and families can access resources, services, and support.
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Fundraisers raise awareness and generate crucial resources for the patient community.
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Back-to-School Town Hall Replay
Starting a new school year can feel overwhelming for families navigating complex lymphatic anomalies (CLAs) or lymphatic malformations (LMs). In this LGDA Town Hall, members of our Patient & Community Advisory Council share practical tips, personal experiences, and resources to help students succeed—academically, socially, and emotionally.
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