Yoga for Lipedema
« All Events Yoga for Lipedema Movement Matters Instructor Diana Instructor: Diana “Movement Matters” First and foremost using yoga as a safe way to move. Added benefits are better individual […]
$96
« All Events Yoga for Lipedema Movement Matters Instructor Diana Instructor: Diana “Movement Matters” First and foremost using yoga as a safe way to move. Added benefits are better individual […]
Join us for the Lipedema Manitoba Meet-Up, an evening dedicated to shared experiences, support, and learning! Discover insightful discussions on manual lymphatic drainage treatments and the benefits of pneumatic compression pumps. Our guest speaker, Susan Zwarich RMT, CLT, is a community expert who will share her valuable insights on specialized care for lipedema patients. Whether you’re living with lipedema or simply curious to learn more, this event is a perfect opportunity to connect with others who understand your journey. Enjoy refreshments, engage in meaningful conversations, and help support the Lipedema Manitoba Association with a suggested donation of $5.
Join us for a live stream event on Lipedema Reduction Surgery with experts Dr. Mojtaba Ghods and Dr. Giw Mostofizadeh from Ernst Von Bergmann Klinik, Germany. Discover insights into lipedema management and surgical options. Engage directly with specialists during our live Q&A session. Mark your calendars for March 14th, 2025, and don’t miss this opportunity to learn and connect! Tune in live on YouTube!
Join us for an empowering webinar with Diana Dimmock, founder of Accessibility 4 Every Body and a passionate advocate for inclusivity and self-advocacy. Diagnosed with lipo-lymphedema at 34, Diana transforms her experiences into meaningful support for others. Discover how to build a local support network, host virtual gatherings, and advocate for yourself in medical settings. Learn practical strategies to foster connection and resilience within the Lipedema community. Whether you're newly diagnosed or seeking ways to empower yourself and others, this session is designed for you. Let’s unite to strengthen our Lipedema community together!
Rejoignez notre groupe de soutien virtuel pour le lipœdème et entrez en contact avec d'autres personnes qui comprennent votre parcours ! Dans cet espace en ligne accueillant, vous aurez l'occasion de partager vos expériences, d'acquérir des connaissances et de nouer des amitiés durables avec d'autres membres de la communauté vivant avec le lipœdème. Nos appels de 60 minutes encouragent un dialogue ouvert, alors apportez vos appareils photo et vos micros pour une atmosphère engageante et encourageante. Que vous soyez à la recherche de conseils, d'encouragements ou simplement d'une discussion amicale, cette rencontre est faite pour vous. Ne manquez pas la chance de faire partie d'une communauté compatissante qui comprend vraiment ce qui se passe - rejoignez-nous et sentez le soutien !
Join our Virtual Lipedema Support Group and connect with others who understand your journey! In this welcoming online space, you'll have the opportunity to share experiences, gain insights, and build lasting friendships with fellow community members living with lipedema. Our 60-minute calls encourage open dialogue, so bring your cameras and mics for an engaging and supportive atmosphere. Whether you're seeking advice, encouragement, or simply a friendly chat, this meet-up is designed for you. Don't miss out on the chance to be part of a compassionate community that truly gets it—join us and feel the support!
Get ready for an unforgettable experience at the 3rd Annual LymphyCON Health Conference on April 26 & 27, 2025, at Calgary Delta South! This isn’t just a conference; it’s a vibrant celebration of lymphatic health, bringing together professionals, patients, and researchers for an action-packed agenda. From inspiring speakers and interactive workshops to networking opportunities and a unique Compression Garment Fashion Show, there’s something for everyone! Plus, enjoy delicious refreshments throughout the event to keep your energy high. Don’t miss out on this chance to connect, learn, and have fun in a supportive community!
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 […]
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!
