The August Lipedema Patient Roundtable was a star-studded hour featuring exciting developments in the world of lipedema from special guests Karen Ashforth and Susan O’Hara.
From GLP-1 drugs and surgical treatments to getting the courage to wear compression garments in public, it was conversational fireworks at the July Lymphedema Patient Roundtable!
Explore clinical evidence in over thirty peer-reviewed publications. View studies on Lympha Press activating the lymphatics using near-infrared imaging.
Brittany Williams’s determination to get treatment for her daughter’s lymphedema sparked the creation of a pediatric lymphedema nonprofit, summer camp, and for-profit.
The June 2024 Lipedema Patient Roundtable marked the fourth anniversary of the online gathering. To celebrate, anchor panelists invited their favorite “chatters” to join them for the conversation — and celebration — this Lipedema Awareness Month.
Whether you live with lipedema, treat people who have it, or never even heard the word before: You’re bound to learn something new from Dr. Herbst’s presentation!