The July Lipedema Patient Roundtable focused on hope, practical strategies, and the importance of community as patients navigate life with lipedema.
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The panel reflects on Camp Watchme, answers questions from the audience, and explores what it means to live fully with lymphedema at every stage of life.
Lipedema often remains undiagnosed for years. Learn signs, treatment goals and self-management tools that support better care.
July’s Research Roundtable featured an engaging discussion exploring how lifestyle medicine can improve outcomes for people living with lipedema, lymphedema, chronic venous insufficiency, and related fat disorders.
The June Lipedema Patient Roundtable celebrated Lipedema Awareness Month with an evening focused on advocacy, visibility, and the power of community.
The June Lymphedema Patient Roundtable brought together patients, advocates, and clinicians for an engaging conversation in recognition of Wound Care Awareness Month.
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.