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24
Feb
Featuring special guest Emma Cloney of Lipedema Canada, this conversation explored sustainable self-care, mindset shifts that turn routines into acts of self-respect, and how to build more collaborative, bias-aware healthcare relationships.
Published: 24 February, 2026
21
Apr
Workplace advocacy, self-care, and community connection were the focus of the April Lipedema Patient Roundtable, featuring special guest Susan O’Hara, founder of the American Lipedema Association (ALA).
Published: 21 April, 2025

Let's get social!

We’d love to connect with you.

Contact Us.

We're ready to help.

Looking for more information, or to be connected with your local representative?
We can help. Fill out our contact form to get started.