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For many women diagnosed with Lipedema, the healthcare journey can feel fragmented.
One provider focuses on surgery. Another discusses compression. A physical therapist addresses recovery. A nutritionist talks about inflammation. Patients are often left trying to connect the dots themselves while navigating a condition that remains widely misunderstood.
Lipedema Team was built around a different idea.
As one of North America’s first fully integrated Lipedema care centers, Lipedema Team brings together surgeons, physical therapists, rehabilitation specialists, nutrition support, compression therapy, and long term patient care within a single coordinated model. Rather than treating Lipedema through isolated appointments and disconnected recommendations, their goal is to create a comprehensive experience that supports patients through every stage of their journey.
As Presenting Sponsor of the Lipedema Summit, Lipedema Team is helping bring that philosophy to a global audience while advancing education around what multidisciplinary Lipedema care can look like.
Founded by plastic and reconstructive surgeons Dr. Max Sirota Toporek and Dr. José Carlos Martínez López, Lipedema Team was created after both physicians recognized a major gap in Lipedema care. Despite years of medical training and advanced surgical education, they saw firsthand how few providers truly understood the condition and how difficult it was for patients to find coordinated, comprehensive care. Their vision was to build a center where patients could access not only surgical expertise, but also the rehabilitation, education, and long term support needed to manage a chronic disease successfully.
Today, patients travel from across the United States, Canada, Mexico, and beyond to work with a team that understands Lipedema as far more than a surgical condition.
One of the defining characteristics of Lipedema Team is that their care model extends far beyond the operating room.
Patients often arrive carrying years of frustration, failed weight loss attempts, chronic pain, mobility limitations, inflammation, swelling, and unanswered questions. Addressing those challenges requires more than a single treatment plan.
Lipedema Team’s multidisciplinary approach combines surgical care with physical therapy, rehabilitation, compression therapy, nutrition, and ongoing patient education. Their philosophy is that every aspect of a patient’s health influences outcomes, from inflammation and mobility to recovery, mental wellbeing, and long term lifestyle habits.
Rather than focusing solely on symptom management, the team works to help patients better understand their condition and build sustainable strategies for living with Lipedema over the long term.
This patient centered model has become one of the reasons Lipedema Team has earned recognition throughout the Lipedema community and why patients often seek them out after struggling to find answers elsewhere.

While Dr. Max and Dr. José are internationally recognized for their work in Lipedema surgery, both are strong advocates for conservative care and long term disease management.
Throughout the Lipedema Summit, they will discuss topics ranging from foundational Lipedema education and conservative treatment strategies to surgical planning, recovery, revision cases, and the future of Lipedema care. A recurring theme throughout their work is that surgery should never exist in isolation. Nutrition, compression, movement, rehabilitation, and patient education all play an important role in helping patients achieve the best possible outcomes.
Their sessions reflect the same philosophy that guides their clinical work every day: informed patients make better decisions, and successful outcomes require a comprehensive approach rather than a single intervention.
Attendees will hear from Lipedema Team during sessions including Foundations of Lipedema Care, Conservative Treatment Strategies Across Disease Stages, Exploring Foundations of Lipedema Surgery, The Multidisciplinary Model in Lipedema Surgery, Different Approaches to Lipedema Surgery, Revision Cases in Lipedema, When Not to Operate, and discussions focused on the future of long term Lipedema management.
A major part of what makes Lipedema Team unique is the emphasis they place on rehabilitation and recovery.
Nicole Steiner, Physical Therapy Lead at Lipedema Team, specializes in vascular and lymphatic rehabilitation, movement therapy, compression therapy, and post surgical recovery. She plays a key role in helping patients navigate conservative treatment, surgical preparation, rehabilitation, and long term care while supporting patients throughout every stage of recovery.
Her work reflects an important principle within the Lipedema Team model: surgery is only one chapter in a much larger journey.
At the Summit, Nicole will share her expertise during Physiotherapy in Lipedema: From Inflammation to Long Term Care, where attendees will learn more about the role of rehabilitation, lymphatic health, movement, compression, and recovery in helping patients maintain long term results and improve quality of life.

The Lipedema Team sessions span nearly every stage of the patient journey, from diagnosis and conservative care to surgery, recovery, rehabilitation, and long term management.
Whether you are newly diagnosed, considering surgery, supporting a loved one, or simply looking to better understand the condition, their conversations offer valuable insights into the realities of living with Lipedema and the many factors that influence successful outcomes.
Most importantly, their sessions reflect a broader vision for the future of Lipedema care, one that brings together multiple specialties, prioritizes patient education, and recognizes that every individual’s journey is unique.
As Presenting Sponsor of the Lipedema Summit, Lipedema Team is helping make education, awareness, and expert conversations accessible to thousands of patients, caregivers, and healthcare professionals around the world.
Visit their virtual booth to learn more about their multidisciplinary approach, meet the team, and access additional educational resources.
Booth:
https://event.lipedemasummit.com/sponsors/lipedema-team/
Website:
https://www.lipedema.team/
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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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