Linda Anne Kahn discusses the fascia and explains how trauma is stored in the tissues. The talk also explores the connection between the heart, the brain, and the vagus nerve and identifies how it relates to Dercum’s disease, lipedema, Ehlers-Danlos syndrome, dysautonomia, and mast cell activation syndrome.
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In this exciting and research-oriented talk with Linda-Anne Kahn, we explore mast cell activation syndrome (MCAS) and the symptoms associated with MCAS.
It was a boo-tiful night to talk about lipedema, especially since Linda Anne Kahn had recently returned from the Lipedema World Congress in Germany. Special guest Dr. Molly Sleigh also joined the panel with takeaways from her time at the National Lymphedema Network Conference in Philadelphia.
Lipedema therapies including massage guns, aromatherapy, and of course, the Optimal Plus by Lympha Press are discussed by experts.
The April 2026 Lipedema Patient Roundtable focused on one of the most important—and often overlooked—aspects of living with lipedema: adapting as your needs evolve, without guilt or shame.
The March Lipedema Patient Roundtable brought together a dynamic group of experts and advocates to share education, updates, and practical strategies in recognition of Lymphedema Awareness Month.
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.
From insomnia and hormonal changes to lipedema-related brain fog, this discussion highlights why sleep is a critical (and often overlooked) part of care.
This month’s Lipedema Patient Roundtable offered a much-needed pause amidst the busyness of the holidays!
The November Lipedema Roundtable explored mast cell activation, chronic inflammation, hormones, and the emotional realities of living with lipedema.