Win Big While Supporting Those Living with Lipedema! – Enter Our 50/50 Raffle Today! We’re thrilled to launch the Lipedema Manitoba Association 50/50 Raffle, helping us raise vital funds to support those affected by lipedema—a chronic condition that causes painful fat accumulation, primarily in the legs and arms. Despite affecting millions of women, lipedema remains widely underdiagnosed...
Join us for a special evening with the Board of Lipedema Canada as we kick off Lipedema Awareness Month! This intimate Fireside Chat offers a unique opportunity to hear directly from our leadership about exciting plans for June. Discover a range of activities, from live webinars to community events and in-person gatherings across Canada. Celebrate our first-year milestones and engage in an interactive conversation about our mission and progress. Whether you're newly diagnosed, a caregiver, health professional, or advocate, this free event invites you to connect, learn, and be part of a growing national movement. Don’t miss out!
In a powerful upcoming episode of the Thrive Beyond Size podcast, Michelle Tubman interviews Diana Dimmock and Emma Cloney from Lipedema Canada, shedding light on the often-misunderstood condition of lipedema. With 1 in 9 women affected, this painful and debilitating condition remains largely unrecognized in Canada, leaving many without proper diagnosis or treatment. Michelle reflects on her own journey as a physician, questioning the medical system that overlooks such a significant issue. Tune in on June 5th to discover the realities of living with lipedema and the urgent need for change in Canadian healthcare.
Join us for an enlightening Zoom webinar that delves into the often-overlooked condition of lipedema. This session offers a unique clinical and patient-centered perspective, featuring a comprehensive head-to-toe assessment guide and addressing the barriers to diagnosis and care. Learn from experts about the impact of lipedema on quality of life, the challenges patients face in Canada, and the importance of interprofessional collaboration. Whether you're a clinician or a patient, this event is designed to enhance awareness and improve early recognition in clinical practice. Don’t miss this opportunity to expand your knowledge and make a difference!
Join us on June 11th at sunset for a breathtaking event, "Lipedema in Lights," as we illuminate the Brant Street Pier in Burlington, Ontario, with vibrant purple lights—the official color of lipedema awareness. This striking display honors those living with lipedema and emphasizes the importance of early diagnosis and community support. Whether you're local or afar, you can participate by visiting the pier or sharing your purple-themed selfies from home. Together, let’s create a powerful visual celebration of strength and solidarity in our community. Don’t miss this chance to shine a light on lipedema awareness!
Join us on June 11, 2025, as the iconic CN Tower glows purple in a stunning display of support for Lipedema Awareness Day! This powerful initiative, organized by Jenn Sephton and supported by Lipedema Canada, aims to raise visibility and foster connection for those living with lipedema. Witness the tower's breathtaking purple lighting during the last 30 minutes of each hour, starting at sunset. Whether you're in Toronto or across the country, you can participate by sharing your photos and joining our community collage. Together, let’s celebrate strength, unity, and advocacy for lipedema awareness!
Discover the intricate relationship between lipedema and menopause in our upcoming webinar! As women (afab) transition through menopause, hormonal shifts can significantly impact their bodies, especially for those with lipedema. Join Dr. Celia Egan, an expert in Obesity Medicine and Metabolic Health, as we delve into how these changes can exacerbate symptoms and what options are available for managing them. This informative session will not only address the safety of hormone replacement therapy for women with lipedema but also provide a platform for your questions during a live Q&A. Don’t miss this opportunity to gain valuable insights!
Join us for an enlightening webinar that uncovers the systemic gaps in lipedema care in Canada. Discover how health equity issues, gendered impacts, and clinician education play crucial roles in the experiences of those living with lipedema. Learn to identify barriers to assessment and care, advocate for improved access, and reflect on the vital role clinicians play in transforming awareness into action. Whether you're a clinician or a patient, this free event offers valuable insights and resources. Don’t miss the chance to be part of this important conversation and help shape the future of lipedema care in Canada!
Join us for Lipedema Trivia Night, a fun and interactive online gameshow celebrating Lipedema Awareness Month! Test your knowledge and learn fascinating facts about lipedema while connecting with our community across Canada. This free event welcomes everyone, whether you're a seasoned advocate or just starting to explore lipedema. Compete for exciting prizes, including a WAVER Vibration Plate, Lipedema Canada prize pack and a pair of Bauerfeind Curaflow Canada compression garments! With live questions on Kahoot and a chance to be an on-camera contestant, it’s an evening you won’t want to miss. Let’s come together to raise awareness and have a blast!
Join Lipedema Canada at the Manitoba Legislature for "Lipedema at the Leg"—our first in-person Lipedema Awareness Month event. Together, we'll raise our voices for the 1 in 9 affected by lipedema and call for the equitable care they deserve.
Wear purple, bring your community, and show your support. Meet our board, connect with service providers, and be part of a powerful movement for change.
End the day with a purple-lit tribute at the Esplanade Riel Bridge and WINNIPEG sign. Let’s make lipedema visible—and unforgettable.
On July 17th, 2025, Germany made a groundbreaking decision to cover liposuction for lipedema at all stages through public health insurance. This historic moment raises important questions for Canada: Will it increase awareness among healthcare providers? Could it pave the way for similar coverage here? Join Lipedema Canada for a special community webinar where we’ll discuss the implications of this decision, explore access to treatment, and outline concrete steps for advocacy. Whether you’re living with lipedema or supporting someone who is, this conversation is vital for shaping the future of lipedema treatment in Canada.
Join Lipedema Canada for a one-hour Fireside Chat as we share updates, insights, and announcements that will shape the year ahead. Our team has just returned from presenting at the World Lipedema Congress in Rome and attending the International Lymphedema Framework conference in Niagara Falls. This event is an opportunity to hear what we learned,...
