Blog

Let's Talk Lipedema

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!

Emma Cloney and Lipedema Manitoba recognized by the Manitoba Government for their advocacy work. Emma Cloney and Angel Anderson pictured outside the legistaure.
Lipedema in the News

The Power of Recognition

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 clinicians. Let’s delve into the significance of official recognition and its impact on the lives of those affected by Lipedema in Canada.

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Lipedema Canada in the News
Lipedema in the News

Lipedema Canada in the News

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 and stories that have surrounded this monumental progress. Our team is dedicated to providing professional support to Canadians affected by lipedema.

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Love letters to my lipedemic self
Real Stories

Love letters to my lipedemic self

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

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