Lipedema Canada

Lipedema Canada Lipedema Canada is the national association for Canadians with lipedema. We are a registered charitable, not-for-profit organization.

We are dedicated to making real change for the lipedema community.

There's so much to learn and to talk about at Canada's first Lipedema Conference.  We're excited to hear from experts in...
08/20/2026

There's so much to learn and to talk about at Canada's first Lipedema Conference. We're excited to hear from experts in their respective fields and folks from our lipedema community. Join us in person or virtually.
https://conference.lipedemacanada.org/

Are you joining us in Winnipeg?
08/18/2026

Are you joining us in Winnipeg?

08/15/2026

The Lipedema Canada model call is closed. Thanks to all who applied!

APPLICATIONS CLOSE SOON!Are you thinking of applying to be a model for our brand photoshoot?  Applications close Friday ...
08/13/2026

APPLICATIONS CLOSE SOON!

Are you thinking of applying to be a model for our brand photoshoot? Applications close Friday August 14! Please send us a brief introduction with your age, height and lipedema stage (if known), along with a recent full body photo of yourself in bike shorts and tank top or sports bra to [email protected]

https://www.facebook.com/share/p/1FEAkWzLdK/Thank you to Sing for a Cause for your generosity!
08/13/2026

https://www.facebook.com/share/p/1FEAkWzLdK/

Thank you to Sing for a Cause for your generosity!

Thank you to everyone who attended our karaoke fundraiser in support of Lipedema Canada. With the generous donations of our community partners and those who attended and donated online, the grand total raised was $1354.00. These funds went directly to support patients who are in need of assistance. A special shoutout to Jenn Sephton for helping this event come to life with the door prizes and raising awareness. 🙂

Be sure to follow Lipedema Canada and our community partners.

CIE Property Management & Consulting
The Gallery Upstairs at Bronte & Mill St.
The Empowered Chick
Julie Lafleur
Anne More Originals
CMG Artworks
The Courageous Middle
Champs Family Entertainment Centre
Singer’s Spotlight Karaoke

Dr. Arya Sharma — a founder and past scientific director of Obesity Canada, and a trusted voices in Canadian medicine — ...
08/11/2026

Dr. Arya Sharma — a founder and past scientific director of Obesity Canada, and a trusted voices in Canadian medicine — is calling for lipedema to be recognized as a confounder in weight-loss trials. His point is one our patients and experienced clinicians have been making for years: lipedema tissue doesn't respond to caloric restriction, and when it goes unscreened, women are left labelled "non-responders" and carrying the weight bias that follows. Screening at baseline is a simple fix, and the time for change in Canada is now.

Read his full post here: https://www.linkedin.com/feed/update/urn:li:activity:7492830593475608576/

• What to Wear to the Gala • Dress code: come dressed up with somewhere to go.Floor length gowns are absolutely welcome....
08/10/2026

• What to Wear to the Gala •

Dress code: come dressed up with somewhere to go.

Floor length gowns are absolutely welcome. So is a suit. So is the dress you have been waiting for an excuse to wear.

And we know something else is true. Finding clothing that fits and feels good with lipedema can be hard, expensive, and exhausting. Some of us have spent years being told what we should not wear. Not here.

Come as you are. Wear the thing that makes you feel most like yourself. Compression is welcome on the red carpet, because it is part of how many of us live well, and there is nothing to hide.

Comfortable shoes and your favourite compression garments are strongly encouraged. The dance floor opens later and you will want them.

There is no wrong way to dress for this evening. Come as you are, dressed up, and ready to celebrate.

September 12. Royal Aviation Museum of Canada, Winnipeg.

Tickets and details: www.lipedemacanada.org/event/gala/

Meet Dr. R. Daniel Hagerty, MD, founder and Chief Medical Officer of Premier Lipedema Clinic in Spokane, Washington, joi...
08/10/2026

Meet Dr. R. Daniel Hagerty, MD, founder and Chief Medical Officer of Premier Lipedema Clinic in Spokane, Washington, joining us at LipCanCon 2026 on September 10–12 in Winnipeg, Manitoba, Canada.

Dr. Hagerty is a board-certified physician who earned his medical degree and a Master of Science in physiology and biomedical engineering at the University of Arizona, then completed his emergency medicine residency and an advanced fellowship in emergency ultrasound through MetroHealth Medical Center, Case Western Reserve University, and the Cleveland Clinic.

For the past seven years his work has centred almost entirely on lipedema. He trained in Germany with Dr. Josef Stutz, one of the pioneering surgeons in lymphatic-sparing liposuction, and has since evaluated and treated hundreds of patients and performed thousands of lipedema reduction procedures. Much of his attention goes to the part that has to come first: telling lipedema apart from other adipose, vascular, and lymphatic conditions, so that everything that follows is built on the right diagnosis. He is also a founding member of the Lipedema Society and sits on its Surgical Committee, helping develop the Surgical Standard of Care for lipedema treatment in the United States.

He joins us as a faculty educator for The Doctor Is In, our pre-conference clinic where Canadian physicians and nurse practitioners learn to assess and diagnose lipedema on real patients. A longtime medical educator and physician mentor, he has spent years working to improve how doctors recognize this condition, and we are honoured to bring that teaching to Canada, where far too many patients are still waiting to be named.

We are inspired by his kind nature and by his ongoing commitment to improving the lives of people with lipedema.
🔗 Register now at conference.lipedemacanada.org

Good news. We extended the deadline. You now have until Wednesday, August 12 to nominate someone for the first Lipedema ...
08/08/2026

Good news. We extended the deadline. You now have until Wednesday, August 12 to nominate someone for the first Lipedema Canada Luminary Awards.

We did that because the nominations coming in have been extraordinary, and we knew there were more stories out there.

We called them the Luminary Awards for a reason.

For most of us, understanding lipedema did not arrive all at once. It came from someone. A clinician who kept learning when it would have been easier not to. A researcher working on questions nobody was funding. An advocate who kept saying the word until a room finally listened. A partner, a parent, a friend who learned how to help and then just kept helping.

They lit the way. Most of them do not know they did it.

These are our first awards, and we want the room to look like the community actually looks. Canadian or not. Clinician or patient or the person who drove you to every appointment. If they made a difference, they belong on that list, and yes, you can nominate yourself.

Tell us who lit the way for you.

Nominate here: https://www.lipedemacanada.org/event/gala/

Nominations close Wednesday, August 12. Winners are announced live at the gala on September 12 in Winnipeg.

Presented by Lipedema Canada, made possible by the generosity of Bauerfeind Canada.

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Winnipeg, MB

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