We are the faces of lymphedema
Lymphedema affects millions worldwide, yet many remain undiagnosed or unaware of effective management strategies. This World Lymphedema Day, we’re shining a light on this condition by providing expert insights and sharing those who successfully manage it every day.
Let’s stand together for awareness and support
Lymphedema affects millions of people worldwide, spanning all ages, backgrounds, and experiences. Despite their differences, they share one common trait: resilience.
On World Lymphedema Day 2025, we stand together to honor those living with this condition. Our video features individuals from around the world, each declaring one simple but powerful truth: “I am a face of lymphedema." Their voices remind us that lymphedema connects many, and no one should face it alone.
Lymphedema is often misunderstood, but knowledge is the first step towards awareness and management. But what exactly is lymphedema?
Lymphedema is caused by damage in the lymphatic system, leading to swelling in the arms, legs, fingers, or other parts of the body. While it's not cancer, it can be triggered by cancer treatments that impact the lymph nodes.
There are two types of lymphedema:
- primary lymphedema is rare and often congenital, appearing around puberty or pregnancy.
- secondary lymphedema develops due to trauma, surgery, radiation, or infections affecting the lymphatic system.
Lymphedema advances through four stages, from mild swelling to severe thickening of the skin. While lymphedema can't be cured, early detection, daily management, and lifestyle adjustments can significantly improve quality of life.
Find more information on lymphedema by visiting the pages below.
If you think you have lymphedema, talk to your doctor.
If you suspect you have lymphedema, consulting a healthcare professional is crucial. They can guide you through:
- screening and diagnosis based on your medical history
- symptom management strategies tailored to your condition
- compression solutions to help reduce swelling
- healthy lifestyle choices that support long-term well-being
Lymphedema Treatment Act
New laws drafted under the Lymphedema Treatment Act have expanded Medicare coverage of compression garments for the treatment of lymphedema.
At Sigvaris, we're here to support you. Our solutions are designed to manage and treat complex lymphatic and venous conditions, offering care and comfort for every step of your journey.
Today and every day, we stand with you. Together we raise awareness, share hope, and remind everyone living with lymphedema: you are not alone.
From active treatment to long-term maintenance, Sigvaris products are created with the needs of individuals with lymphedema in mind. With innovative technology, quality craftsmanship, and modern designs, our products restore, assist, and enhance people’s lives.