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. The discussion featured Kathleen Lisson, CMT, CLT—a certified lymphedema therapist and contributor to the U.S. Standard of Care for Lipedema.
A key focus of the conversation was clarifying the distinction between lipedema and lymphedema—two conditions that are often misunderstood and frequently overlap. Kathleen explained that while lipedema is a chronic adipose tissue disorder, many patients also experience a lymphatic component, even if it is not classified as traditional lymphedema. Understanding this nuance is essential for accurate diagnosis, effective treatment planning, and helping patients make sense of their symptoms as conditions evolve.
The panel emphasized a comprehensive, whole-person approach to care. Topics included the role of the lymphatic system, post-surgical therapy, and the impact of stress and trauma on disease progression. Kathleen also highlighted how chronic stress and adverse childhood experiences can influence inflammation and healing, underscoring the importance of addressing both physical and emotional health in treatment plans.
Linda Anne Kahn shared insights from her recent presentations across the country, including emerging conversations around nutrition, hormonal balance, and the growing interest in GLP-1 medications. While these therapies are gaining attention, the panel encouraged patients to stay informed, ask questions, and work closely with knowledgeable providers to determine what’s right for them.
With the rise of scams and AI-generated misinformation, the group also stressed the importance of verifying sources. Trusted organizations such as the American Lipedema Association, the Lipedema Foundation, and Lympha Press were highlighted as reliable resources for accurate information.
Throughout the discussion, one message remained clear: empowerment comes through education and community. Patients were encouraged to advocate for themselves, seek qualified care, and build sustainable routines that support lymphatic health, stress management, and overall well-being.
The session closed with a reminder that managing lipedema is not one-size-fits-all. Progress often comes from a combination of medical care, lifestyle changes, and emotional resilience—strengthened by a supportive community.
Heartbows to this month’s panel:
- Jenny Beaujean (@Jenny_Beaujean)
- Angelique Charles (@TheLippyButterfly)
- Cara Garrett (@PaleGingerPear)
- Linda Anne Kahn (@lindaannekahn)
- Kathleen Lisson (@kathleenlisson)
- Brenda Viola (@BrendaViola_ViciCommunications)
This Roundtable was originally recorded live on March 18, 2026, and has been edited for time. The views and opinions expressed in this Patient Roundtable are those of the individual participants and do not necessarily reflect the official position of Lympha Press.
This video is intended for informational and educational purposes only. It is not a substitute for professional medical advice, diagnosis, or treatment. Always consult your healthcare provider with any questions about your condition or treatment.