Advanced Lipedema Treatment
Internationally renowned, comprehensive program that
address all areas of Lipedema treatment.
💬 For 14 years, Angela lived with pain, limited mobility, misdiagnoses, and uncertainty caused by Lipedema.
She couldn’t work, hike, or even comfortably walk her dog. Then, her daughter found information about Lipedema online and everything began to change.
After receiving a proper diagnosis, Angela came to and the Roxbury Institute for surgery on her trunk and legs. She says she finally feels released from the pain and physical restrictions that had held her back for years.
Within about a month, she began noticing significant changes in her mobility and overall quality of life.
Comment 💜 to celebrate Angela’s transformation!
A little fun and creativity with The Roxbury team from our Utah center! 🎨
We stepped away from the day-to-day for a painting night, and enjoying time together.
Grateful for the people who make our workplace a great place to be.
Comment TEAM to learn more about our work family at the Roxbury Institute! 👇
🤔 Could MCAS be connected to lipedema?
Mast Cell Activation Syndrome (MCAS) may coexist with lipedema and contribute to inflammation, nodules, rashes, hives, and sensitivity to heat or sunlight.
Diagnosis can be challenging because symptoms vary widely and testing isn’t always definitive. A negative test does not necessarily rule out MCAS.
Researchers are continuing to explore the connection between mast cell activation and lipedema to better understand these complex conditions.
Common MCAS to connect with our team if you suspect you may have this condition.
09/22/2026
An important update about Dr. Karen Herbst
Dr. Herbst is transitioning to a reduced clinical schedule as she gradually moves into semi-retirement from her primary clinical practice. This next chapter will allow her to dedicate more time to research, education, and advancing the understanding and treatment of fat disorders.
Patients whose care may be affected by changes to her clinical availability are being contacted directly to discuss their individual needs and next steps.
We’re grateful to continue working alongside Dr. Herbst as she brings her expertise and passion to this next chapter of her work.
If Dr. Herbst has been part of your journey, let us know your favorite memory or share a message of appreciation for her in the comments below.
🙋♀️ For years, Krista wondered why her body felt so different.
From North Carolina, Krista shares her journey of living with lipedema symptoms and the physical and emotional toll that came with not having answers.
After discovering more about lipedema through social media, Krista sought medical guidance and connected with The Roxbury Institute and Dr. Aria, who confirmed her diagnosis. Finding a team that listened, supported her, and understood what she was experiencing brought a sense of validation she had been searching for.
Now, Krista is looking forward to feeling more comfortable in her body, reducing her pain, and getting back to the activities she loves.
Have you had a similar experience finding your diagnosis? Share your story in the comments below.
09/18/2026
📣 Did you hear the news? We’re now accepting insurance! Our announcement has been picked up by media outlets across the country. Read the Associated Press article in our link in the bio!
🗓️ Effective October 15, 2026
✅ Patients seeking specialized lipedema treatment
📍 California
Are you an out of state patient? Good news! You may qualify too. Comment CIGNA to connect with our team to learn about your options.
We’re so grateful to have Melissa Seaton, MSN, FNP-C, representing Advanced Lipedema Treatment and The Roxbury Institute at LipCanCon, Canada’s first national lipedema event. 🇨🇦
Melissa had the opportunity to speak on mast cell involvement and lipedema, sharing insights from her clinical experience and helping bring greater awareness to the complex conditions many patients navigate.
We’re incredibly proud to see Melissa representing the ALT Program on an international stage and contributing to conversations that move lipedema care and education forward.
Interested in learning more? Comment LIPCANCON to connect with Melissa and schedule a consultation!
💅 For many people, a pedicure is relaxing. For someone with lipedema, the pressure and massage can sometimes be surprisingly painful.
One of the hallmark symptoms of lipedema is pain and tenderness in the affected tissue. Inflammation and changes within the adipose tissue can make the legs unusually sensitive to touch and pressure.
These everyday experiences can be important clues that something more than “sensitive legs” may be going on.
What are some unexpected things that cause you pain or tenderness? Let us know down below.
👐 Did you know fibrosis can actually be felt beneath the skin?
Lisa, an MLD therapist with the ALT Program at The Roxbury Institute, explains that fibrotic tissue can feel firm, ropey, or hardened beneath the skin. Its texture can vary depending on where it is located.
That’s why skin-to-skin contact is so important during manual lymphatic drainage. It allows the therapist to better assess the tissue, identify areas of fibrosis, and tailor their techniques accordingly.
Gloves may be used immediately after surgery while incisions are still open to help prevent infection. Once the incisions have fully healed, skin-to-skin treatment allows for a more precise tactile assessment.
Have you ever felt your fibrosis? Share your experience in the comments down below.
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