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For many people, receiving a Lipedema diagnosis can feel like a victory after years of searching for answers. But once that moment of clarity arrives, the next challenge often begins: trying to understand the condition and the many options surrounding care.
There is a growing amount of information available, but much of it can feel overwhelming, highly technical, or presented in formats that are difficult to follow.
Our goal is simple:
To deliver clear, accessible, and trustworthy education that helps people make informed health decisions.
The summit brings together clinicians, surgeons, therapists, researchers, and patient advocates to share their knowledge in one place. The intention is not to direct people toward a single pathway, but to help individuals better understand the options available and how to thoughtfully navigate their care.
The experience is designed to be patient-forward, while still offering meaningful insights that clinicians, practitioners, and educators can find valuable and share within their own communities.
Every decision about the summit is guided by five core principles.
1. Education That Is Easy To Follow
Lipedema is complex, and many people encounter overly technical explanations or confusing information online. The summit focuses on clear conversations that break down complex topics into understandable insights..
2. Broad Accessibility
The event is free to attend during the live broadcast so that anyone seeking information can access it without financial barriers.
3. Transparency And Trust
Sessions are designed to be educational conversations, not promotional presentations. Experts share perspectives, research, and clinical insights so attendees can evaluate information and decide what is right for them.
4. A Meaningful Experience
The summit brings together both patient experiences and clinical expertise. This combination helps validate lived experiences while providing deeper medical context.
5. High Quality Production
Health education deserves the same care and professionalism as any other important subject. Sessions are recorded in professional studio environments to create a clear, focused viewing experience that respects the audience’s time and attention.
One of the most important decisions we made was to make the summit free to attend live.
Access to education should not depend on someone’s ability to pay.
During the event, attendees can watch sessions as they are released over the three summit days. This approach allows the event to remain accessible while encouraging people to participate during the live experience. Attendees are encourages to organize their schedule and will receive notifications no the sessions they don’t want to miss.
For those who prefer more flexibility, there is also an optional All-Access Pass.
We will also share short video recaps and session summaries throughout the event. By following our social media channels, attendees will be able to revisit highlights and continue learning from the conversations long after the summit concludes.
The All-Access Pass is designed for people who want the ability to review the information at their own pace.
It includes:
• 12-month access to the summit recording library
• Access to sponsor spotlight sessions
• Downloadable PDF session summaries
• Post-event integration email series
This option is intentionally kept low cost and high value so that people who want continued access to the educational archive can revisit sessions when needed.
Early Bird pricing is available until May 1, 2026.
The All-Access Pass does not include VIP sessions or bonus events, which are reserved for separate upgrades.
Producing a large educational event requires significant coordination and resources.
Recording sessions with medical experts, producing high-quality video, coordinating speakers, hosting the event platform, editing content, and distributing the summit to thousands of people all require significant time and investment.
Many of the speakers are traveling to Los Angeles to record their sessions, often at their own expense, reflecting their commitment to advancing Lipedema education and supporting the community.
We encourage attendees to follow and support our speakers, and a simple message of thanks for their time and contribution to this event is always appreciated.
The optional replay pass helps support:
• professional video production
• hosting and platform infrastructure
• editing and educational materials
• ongoing awareness and education efforts
• the ability to produce future summits
When attendees choose to purchase replay access, they are helping support the continued effort to bring credible Lipedema education to a broader audience.
One of the most important principles of the Lipedema Summit is that the content remains education-first.
Sessions are structured as conversations and expert discussions rather than product or treatment promotions. The goal is to give attendees the context and understanding needed to make informed decisions about their health.
This is also why the summit features leading researchers and clinicians in the field.
Among them is Dr. Karen Herbst, a recognized authority in Lipedema research and clinical care, who supports the mission of the summit and will serve as one of the keynote speakers.
By bringing together respected experts from multiple perspectives, the summit helps attendees hear thoughtful discussions rather than a single viewpoint.
The Lipedema Summit exists because thousands of people are still searching for clear answers about this condition.
For many attendees, the summit may be the first time they hear their experiences validated by clinicians who understand Lipedema.
Education, awareness, and better conversations around this condition are long overdue.
This summit is one step toward helping that happen.
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If you've spent years being told to simply eat less and move more while your lower body stays stubbornly disproportionate […] Read more
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· Aug 26, 2026

News
Physicians continued discussing evolving standards of care. Patients shared personal stories and treatment experiences. Sponsors, clinicians, and wellness partners answered questions while new connections formed between people who, only hours earlier, had been strangers. It was perhaps the clearest sign that the 2026 Lipedema Summit Live Event had achieved its purpose. Held on June 11, 2026, in Downtown Los Angeles, the event brought together patients, clinicians, surgeons, researchers, therapists, advocates, caregivers, and industry partners for an evening centered on education, awareness, and connection. While the virtual Lipedema Summit was designed to reach thousands of people around the world, the live event created something equally valuable: the opportunity for meaningful conversations to happen face-to-face. Throughout the evening, attendees engaged directly with leading experts, explored emerging research, discussed treatment approaches, and exchanged experiences with others navigating similar challenges. Conversations ranged from evolving standards of care and surgical outcomes to conservative therapies, patient advocacy, and the future of Lipedema research. For many attendees, the event offered something difficult to find elsewhere: direct access to experts, honest conversations, and the opportunity to connect with others who truly understand the realities of living with Lipedema. Long after the final panel concluded, those conversations continued, reflecting both the growing momentum within the Lipedema community and the shared commitment to advancing awareness, education, and patient care.
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· Jun 21, 2026

Sponsor Feature
When most people think about Lipedema, they think about abnormal fat accumulation. They think about disproportionately larger legs, pain, tenderness, easy bruising, and the frustration of trying countless diets and exercise programs without seeing meaningful changes.
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· Jun 1, 2026

Sponsor Feature
For many women living with Lipedema, finding a surgeon is only part of the challenge. Finding a team that truly understands the disease is often much harder.
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· Jun 1, 2026

Sponsor Feature
For many women diagnosed with Lipedema, the healthcare journey can feel fragmented.
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· Jun 1, 2026

Sponsor Feature
GLP 1 medications have changed the conversation around obesity, metabolic health, inflammation, and chronic disease. For many patients, they have opened doors that previously felt out of reach. Yet as these medications become more widely available, a new challenge has emerged: access does not always equal quality care.
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· Jun 1, 2026

Sponsor Feature
Most Lipedema patients eventually learn that compression is one of the most important parts of conservative care.
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· Jun 1, 2026

Summit Info
The 2026 Lipedema Summit brings together an extraordinary lineup of surgeons, physicians, researchers, therapists, advocates, and patients for three days of conversations focused on diagnosis, treatment, recovery, long-term management, and the future of lipedema care.
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· May 25, 2026

Education
Lipedema is often discussed as a physical condition, one that affects fat distribution, lymphatic health, and metabolic function. But for the millions of women living with Lipedema, the emotional wounds can run just as deep as the physical ones. The reflection in the mirror that no longer feels like you. The constant comparisons. The judgment from strangers, doctors, and sometimes even the people closest to you. These experiences leave marks that go far beyond the body.
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· Mar 15, 2026

Education
Lipedema is a chronic medical condition that affects the way fat is distributed in the body. It most commonly appears in the legs, hips, and sometimes the arms, while the hands and feet are typically unaffected.
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· Mar 13, 2026
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