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
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You are not alone in your battle with lipedema! Our Lipedema Canada blog is here to offer support, empowerment, and resources to help you on your journey. Let’s dive in and conquer this together!
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
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
Let’s Talk – Lipedema Reduction Surgery Live event – June 24th 2024 6pm central time Join the Lipedema Canada team to learn more about Lipedema
The importance of recognition when it comes to the medical condition called lipedema. Our focus will be on raising awareness and providing lipedema education for
The Lipedema Manitoba Association and West End Cultural Centre are hosting the first Lipedema Inclusive Size Inclusive Clothing Swap in Winnipeg on June 2nd from
Jerusha shares heartfelt letters to her younger self as she journeys through life with end stage lipedema.
You’ve been told your chronic illness is
It’s been an exciting 10 months for Lipedema Canada!
As a volunteer-run organization, we’re proud of what we’ve accomplished so far and thank you for your support.
WE NEED YOUR HELP to keep building resources for our lipedema community and to ramp up our advocacy for treatment options in Canada.