Connect with these organizations to get lymphedema help and support.
You can take control of your survivorship with simple, early lymphedema detection – before it becomes chronic.
The Lymphatic Education & Research Network (LE&RN) is an internationally recognized non-profit organization founded in 1998 to fight lymphatic diseases (LD), such as lymphedema (LE), lipedema (LI), and lymphatic malformation (LM), through education, research and advocacy.
Email: lern@lymphaticnetwork.org
The LIVE Today Foundation supports the survivor and healthcare professional community through education, and is the only nonprofit to provide compression garments to survivors with lymphedema because of their inability to pay. Learn more about the LIVE Today foundation.
Email: info@live-today.org
The Lymphedema Treatment Act (LTA) is a federal bill that aims to improve insurance coverage for the medically necessary, doctor-prescribed compression supplies that are the cornerstone of lymphedema treatment.
If you’re a Lymphedema Patient Advocate, we applaud you! We also want to help you advocate for early detection of lymphedema and intervention programs that put patients back in control. Learn more and discuss with patients how SOZO® Digital Health Platform with L-Dex® can make a difference in their survivorship.
You can take control of your survivorship with simple, early lymphedema detection – before it becomes chronic.