2026 NLN Community Partners
The National Lymphedema Network is proud to collaborate with organizations that share our dedication to advancing lymphatic health, patient education, and community support. Together, we strengthen awareness, expand access to care, and empower individuals affected by lymphatic conditions.
Explore our community partners below to discover additional programs, resources, and opportunities that reflect our shared commitment to improving lives through collaboration and compassion
Community Partners
BrCAcademy.org offers compassionate, physical‑therapy–based education and resources to support individuals living with and beyond breast cancer. Created by oncology physical therapist Jodi Winicour, the platform provides clear, empowering guidance to help patients understand pain, navigate treatment, and reconnect with their emotional and physical well‑being.
The Head and Neck Cancer Alliance (HNCA) is a national nonprofit dedicated to providing hope, support, and education to individuals impacted by head and neck cancer. Through free screenings, patient and caregiver resources, survivorship programs, and nationwide awareness initiatives, HNCA works to promote prevention, early detection, and improved quality of life for everyone facing these diseases. The Alliance also amplifies survivor voices, connects families with expert guidance, and advocates for better outcomes across the head and neck cancer community.
Imerman Angels is a nationally recognized nonprofit that provides free, one‑on‑one peer support for anyone impacted by cancer. Their model connects individuals with trained “Mentor Angels” who have lived through a similar diagnosis, treatment, or caregiving experience—offering understanding, hope, and practical guidance from someone who truly gets it.
The International Lipoedema Association (ILA) advances evidence‑based understanding, diagnosis, and treatment of lipoedema worldwide. Through education, research, and global collaboration, the ILA supports healthcare professionals and individuals living with lipoedema, promotes best clinical practices, and works to dispel misinformation with clear, science‑driven resources.
The Lymphangiomatosis and Gorham’s Disease Alliance (LGDA) connects patients, families, clinicians, and researchers to bring clarity, community, and progress to isolated lymphatic malformations and complex lymphatic anomalies. They provide plain-language education, guidance on next steps, connections to expert care, and access to a supportive global community. Because no one should have to navigate this journey alone.
The Lymphedema Advocacy Group is a nonprofit organization dedicated to improving insurance coverage and access to care for individuals living with lymphedema. Founded and led by Heather Ferguson, the group successfully championed the Lymphedema Treatment Act, ensuring coverage for essential compression supplies under Medicare. Through education, collaboration, and legislative advocacy, the organization empowers patients and clinicians to advance equitable care and awareness nationwide.
Become Part of the NLN Community
Explore NLN membership to access trusted resources, meaningful connections, and opportunities to stay engaged across the lymphatic community. Whether you are looking to learn, connect, or deepen your involvement, membership offers valuable ways to stay connected to the mission.