LINFA | Associação Nacional de Doentes Linfáticos is dedicated to improving knowledge of lymphedema, lipedema, and rare vascular diseases in Portugal. We are a patient association that seeks to establish national and international networks to find the best solutions for patients with primary and secondary lymphedema, rare vascular diseases, and lipedema, as well as their families and caregivers. Our goal is to actively participate in all processes where we are mentioned, promoting discussions and essential solutions in the social and healthcare policy areas.

We also focus on promoting knowledge and health literacy within the community. At LINFA, patients, families, and caregivers can find a multidisciplinary network that provides validated answers and support in improving healthcare and quality of life. Join us in our mission to enhance the well-being of those affected by these conditions