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.
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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.
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.