Lymphedema Warriors Association Uganda
We are a dedicated team of individuals passionate about supporting and empowering those affected by lymphedema. Our mission is to provide comprehensive resources, education, and advocacy to enhance the quality of life for individuals with lymphedema, and to promote awareness and understanding of this condition among healthcare professionals and the general public.
Our Story
The Lymphedema Warriors Association was founded by Kushaba Lawin and Nabirye Irene, individuals living with lymphedema who intimately understand the physical, emotional, and financial challenges that come with this condition. Driven by their personal experiences and a shared passion to help others navigate the complexities of lymphedema, they brought together a dedicated team of professionals and advocates to create a supportive community and provide vital resources for those affected. The organization’s mission is to empower patients, families, and caregivers through educating, advocacy, and support, ensuring that no one faces lymphedema alone. By promoting awareness, advancing local research, and advocating for access to quality care, the Lymphedema Warriors Association strives to make a meaningful difference in the lives of those affected, ultimately improving their overall health, well-being, and quality of life.
Our Values
– Compassion: We care deeply about the well-being of our community and strive to provide empathetic support.
– Empowerment: We aim to educate and equip individuals with the knowledge and tools necessary to manage their lymphedema.
– Inclusivity: We welcome and embrace individuals from diverse backgrounds and experiences.
– Collaboration: We work together with healthcare professionals, organizations, and advocates to advance our mission.