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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.
There was something special about the energy in the room from the moment guests arrived.
Throughout the evening, conversations unfolded between people from very different backgrounds who shared a common goal: improving the lives of those affected by Lipedema. Patients exchanged experiences, treatment journeys, and practical advice. Physicians discussed emerging research, evolving standards of care, and new treatment approaches. Caregivers, advocates, therapists, and wellness professionals connected around ways to better support the Lipedema community.
The audience reflected the collaborative spirit of the event, with approximately half of attendees representing the patient community and half coming from the medical, professional, research, and industry sectors.
For a condition that remains widely misunderstood and frequently underdiagnosed, bringing so many perspectives together in one room felt particularly meaningful. The event created opportunities not only for education, but for genuine dialogue between those living with Lipedema and the clinicians, researchers, and advocates working to advance awareness, treatment, and patient outcomes.
One of the highlights of the evening was the live physician panel and moderated audience Q&A featuring leading experts in Lipedema research, treatment, and patient care.
Attendees had the opportunity to hear directly from physicians and clinicians as they addressed a wide range of topics, including conservative treatment strategies, surgical outcomes, recovery protocols, compression therapy, lymphatic health, and the future of Lipedema care.
The discussion reflected one of the core goals of the event: creating opportunities for meaningful dialogue between patients and the experts working to advance the field.
What made the evening particularly impactful was that the conversations did not end when the panel concluded. Questions raised on stage continued throughout the venue as attendees gathered in small groups to exchange perspectives, share experiences, and continue discussions with physicians, clinicians, and fellow community members.
For many attendees, the opportunity to engage directly with experts in an approachable setting was one of the most valuable aspects of the event. Equally important was the chance to connect with others who understood the realities, challenges, and complexities of living with Lipedema, creating a sense of community that extended well beyond the formal program.

A special thank you goes to Prestige Aftercare, the Evening Presenting Sponsor of the 2026 Lipedema Summit Live Event.
Prestige Aftercare provides concierge post-operative and recovery support throughout the Los Angeles area, helping patients navigate the critical healing process following surgery. Their commitment to patient-centered care and recovery made them a natural partner for an event focused on improving outcomes and quality of life for the Lipedema community.
Their support helped make this gathering possible, and their team was actively engaged throughout the evening connecting with attendees and sharing valuable recovery resources.
The event also featured a number of organizations helping advance education, treatment, recovery, and innovation within the Lipedema community.
We would like to recognize:
Each organization plays an important role in supporting patients through research, treatment, recoery, compression, education, advocacy, and ongoing care.


In addition to our featured sponsors, we are grateful for the support of several wellness and lifestyle brands who helped make the evening memorable through product contributions, refreshments, giveaways, and attendee experiences.
Their generosity helped create a welcoming and engaging environment while introducing attendees to products and services aligned with wellness, recovery, and healthy living.



While the Lipedema Summit reached thousands of people online, the live event offered something equally important: human connection.
It created a space where patients could feel seen and supported, clinicians could share knowledge, partnerships could form, and meaningful conversations could continue beyond the screen.
Most importantly, the evening demonstrated the growing momentum within the Lipedema community. From patients seeking answers to clinicians advancing standards of care, researchers pursuing new discoveries, and advocates raising awareness, there was a shared sense that meaningful progress is being made.
To everyone who attended, spoke, volunteered, sponsored, partnered, and helped bring the evening to life, thank you.
The inaugural Lipedema Summit Live Event was more than a gathering. It was a reflection of what is possible when patients, clinicians, researchers, advocates, and industry leaders come together with a shared commitment to improving awareness, education, treatment, and outcomes for those affected by Lipedema.
Together, we are helping build a future where Lipedema is more widely recognized, better understood, and supported by stronger networks of care, research, education, and community than ever before.
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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
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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

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

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· Jun 1, 2026

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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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