Lipedema Canada in the News

let's review the Lauch Week press!

Get ready to be inspired! We’ve had an incredible week leading up to the grand reveal of our brand new website and the start of monumental progress as Lipedema Canada. Let’s take a moment to revisit the amazing articles and stories that surround the launch of essential resources for Canadians living with lipedema.

Organization aiming to help people living with lipedema find resources and healthcare launching in Canada

Manitobans at the forefront of new non-profit created to help people living with lipedema

Winnipeg woman shares story of diagnosis and road to recovery from lipedema

After years of healing from chronic illness, Winnipeg nurse and musician getting back to what she loves

A big thank you to Joanne Roberts of City News and Rachel Ferstle at CBC for celebrating our stories. We are so grateful for your support in getting our message out to the public.

As we launch this exciting initiative, we are filled with hope for the future of lipedema management in Canada. With your help, we can continue to make meaningful changes to how this condition is understood and treated. Our community is stronger than ever, and we are committed to working together to achieve lasting change.

Thank you again for your support and encouragement. This truly is a great day for all of us.

Happy Launch!

– Lipedema Canada team

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Dear LipCan: In-The-Dark

In a heartfelt letter, a young woman shares her struggles with lipedema, feeling defeated by the financial burden of necessary treatments. Despite her efforts to embrace her body, she longs for support and understanding. LipCan responds with empathy, acknowledging the challenges many face in seeking help for this condition. They highlight the importance of community and self-acceptance while advocating for change in insurance coverage. Discover how Lipedema Canada is working to raise awareness and support those affected, and learn about resources available to help navigate this journey. You are not alone in this fight for recognition and care.

Dear LipCan blog seeking surgery in Canada.

Dear LipCan: Surgery-Seeker

Discover the heartfelt support of our vibrant community at ‘Dear LipCan,’ where we address your pressing questions about lipedema and surgery. We understand that navigating the world of surgical options can be overwhelming, filled with varying opinions and experiences. Our commitment is to empower you with knowledge and compassion, guiding you through the complexities of this condition. Join us as we share valuable insights, tackle common concerns, and foster a sense of belonging among those affected by lipedema. Your journey matters, and together, we can illuminate the path to understanding and healing.