The June Lymphedema Patient Roundtable brought together patients, advocates, and clinicians for an engaging conversation in recognition of Wound Care Awareness Month.
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During Lipedema Awareness Month, Dr. Karen Herbst sat down with Dr. Patrick Greaney to explore current surgical approaches, the emerging role of GLP-1 medications, and exciting developments shaping the future of care.
Jenny Beaujean’s lipedema diagnosis came later in life. She shares her journey and offers advice to help others take the first step toward healing.
The May Lipedema Patient Roundtable tackled some of the biggest questions in the lipedema community, from the connection between lipedema and EDS to inflammation, nutrition, manual lymph drainage, and mental health.
People with chronic venous insufficiency (CVI) and lymphedema are often underdiagnosed or undertreated. Learn the signs and how these two conditions interact.
In recognition of Mental Health Awareness Month, this Roundtable explored the complex intersection of mental and emotional well-being with life alongside lymphedema.
Dr. Karen Herbst and Dr. Antonio J. Forte take a closer look at lymphovenous bypass, including patient selection, imaging considerations, and clinical outcomes.
Medicare added a step before some patients can receive pneumatic compression devices. Read about the change and how Lympha Press handles the entire process for you.
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 April Lymphedema Patient Roundtable focused on one of the most important (and sometimes most frustrating) parts of managing lymphedema: compression.