For years, people with lipedema have heard some version of the same sentence: there’s no proof lipedema surgery can help....
New Alliance Improves Support for Canadians Living with Lipedema and Lymphedema
Lipedema Canada and the Lymphedema Association of Ontario have affiliated to better support Canadians living with lipedema, lymphedema, or both. The two organizations are connecting their communities to a broader network of care, making it easier to find reliable information and resources for two closely linked conditions that are too often confused, underdiagnosed, and under-supported.
Canada is Lit Up for Lipedema
June 11th is Global Lipedema Awareness Day, and this year, Canada is glowing up! More than 85 landmarks across the country will turn purple to raise awareness for a condition that affects millions of Canadians. Lipedema impacts as many as one in nine women and those assigned female at birth, yet many remain unaware of it. Visibility is crucial; when a landmark lights up, it sparks curiosity and conversation. Join us in this national effort to shed light on lipedema, show your support, and help those affected feel seen. Find your city and be part of this transformative movement!
Canada is Failing People with Lipedema and Recognition is the First Fix
Canada is failing millions living with lipedema, a painful condition characterized by abnormal fat accumulation, primarily affecting women. Despite affecting an estimated 2.2 million Canadians, lipedema remains unrecognized by the government, leaving patients without proper diagnosis or care. Other countries, like Germany, have taken significant steps to acknowledge and treat this condition, but Canada remains stagnant. A petition is now open, calling for formal recognition of lipedema as a medical condition. This is a crucial opportunity to break the silence and push for change. Discover how you can help make a difference and support those affected.
Announcing LipCanCon: Canada’s First National Lipedema Conference
Join us for LipCanCon, Canada’s first national lipedema conference, on September 11 and 12, 2026, in Winnipeg, Manitoba! This event will unite patients, advocates, and healthcare professionals to enhance the understanding and treatment of lipedema. Experience research presentations, hands-on learning, and discussions that will shape Canadian healthcare's future. Don’t miss this chance to connect with experts and community members. Stay tuned for details at conference.lipedemacanada.org!
Historic Milestone: Manitoba Becomes the First Province in Canada to Recognize Lipedema Awareness Day
Manitoba has made history by becoming the first province in Canada to officially recognize June 11th as Lipedema Awareness Day, a significant step in the fight for better understanding and care for those affected by this often misunderstood condition. This landmark announcement, made by the Honourable Uzoma Asagwara, reflects a commitment to increasing awareness and support for individuals living with lipedema. Join us in celebrating this milestone and learn how you can contribute to advancing lipedema recognition and care across Canada. Together, we can make a difference for the lipedema community!
Germany Approves Public Coverage of Liposuction for Lipedema for All Stages Based on LIPLEG Study
Berlin, July 17, 2025 – In a landmark decision, Germany’s Federal Joint Committee (G-BA) has approved public health insurance coverage...