This November, the conversation gets bigger!!

Join Dr Liza at the Lympha Press Lipedema Patient Roundtable.

For our November monthly educational event, we are stepping outside are usual webinar format and joining a larger conversation about living with Lipedema. You’re invited to be a part of it.

Free to Attend · Nov 18th · 5pm PST (6pm MST, 7pm CST, 8pm EST)

A smiling female doctor with dark, wavy hair in a well-lit medical office, wearing a white lab coat and a stethoscope around her neck.
A smiling female doctor with dark, wavy hair in a well-lit medical office, wearing a white lab coat and a stethoscope around her neck.

We didn't build Lipedema Warrior Clinic because lipedema looked simple. We built it because our own family learned it wasn't. After years of chasing answers, surgery, and conventional advice, we discovered the real story was bigger than lipedema alone. By connecting the dots between the gut, hormones, immune system, inflammation, and connective tissue, we began seeing patterns that traditional approaches were missing. What started as a journey to help one woman became a whole body roadmap that has helped others find answers, reduce inflammation, regain mobility, and finally understand what their symptoms have been trying to tell them. This webinar shares the insights we wish we'd had from the beginning.

Lipedema Rarely Exists in a Vacuum

Let’s Connect with other patients and specialists that can help you along your journey

Women with diagnosed or suspected lipedema who:

  • Also have or suspect MCAS, EDS/hypermobility, POTS, endometriosis, or hormone-related symptoms

  • Experience symptoms that seem to cross multiple body systems

  • Flare despite doing the things they were told should help

  • Feel like recommendations for one condition sometimes make another condition worse

  • Have collected multiple diagnoses but no one has helped connect them

  • Want to understand the biology behind their symptoms rather than simply being handed another protocol

Who is this NOT for:

  • Anyone looking for one supplement, medication, diet, or treatment that “fixes” lipedema

  • Anyone expecting every woman with lipedema to have the same underlying drivers

  • Anyone looking for a one size fits all treatment protocol

REGISTER WITH LYMPHA PRESS

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REGISTER WITH LYMPHA PRESS 〜

You Will Walk Away With Understanding

FAQ’s

Join Women Just like You on a Personal Journey

★ ★ ★ ★ ★

"I followed their plan and within a month I lost 20 pounds. Dr. Liza is very thorough and Angela is very supportive. Together they create the perfect environment to help take control of your health. If you are struggling with lipedema and looking for answers and treatment I can't recommend Lipedema Warrior Clinic highly enough."

★ ★ ★ ★ ★

"I felt so heard, understood, and BELIEVED during my intake. Anyone living with hypermobility, chronic pain, lipedema, or in a bigger body knows how truly rare that is. She made lab recommendations for my PCP, so blood work can be covered through insurance. I feel like I finally have a plan for taking back my health after years of steroids stole it away."

★ ★ ★ ★ ★

"I could barely walk up stairs or from my living room to the kitchen. I was tired all day long even after 10 hours of sleep… After working with Lipedema Warrior Clinic, I learned there were a lot of foods that were creating inflammation in my body. Once I adjusted my foods, I dropped almost 30 pounds of water weight in just three to four weeks and I am able to breathe again, walk up stairs, and just walk in general."