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!
Angel’s triumphant and heartfelt account of navigating lipedema surgery abroad.
“Once I learned about the condition and realized it was so obvious I had it, I was frustrated that no medical professional had mentioned it to me before.”
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 killing you and you have mere months to live. One day, completely out of the blue, your oldest son says, “Mom, why don’t you find
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
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
Lipedema Canada is proud to unveil our new website and essential resources for individuals living with lipedema. Join us in reflecting on the incredible articles