; lipedema Archives - Page 3 of 6 - Lympha Press

Lipedema is a chronic and, in many cases, progressive disease. Over 25% of those diagnosed with this loose connective (fat) tissue disease also suffer from depression. Dr. Karen Herbst explores the mind/body connection and how stress affects the extracellular matrix, which is the support system to all body functions. The role of inflammation and recommendations on how lipedema patients can reduce stress are also reviewed.

Dr. Herbst discussed the groundbreaking Standard of Care publication, which can be accessed here. She also reviewed the importance of mental health and recommended the following links:

For those intrigued by her discussion of Interpersonal Sensitivity, click here to review a “symptom checklist.”

Watch more webinars from our Lympha Press Education Series on YouTube.
June 14, 2021

Mind, Body & The Matrix – The Role of Pumps and Other Therapies for Lipedema

Dr. Herbst explores the mind/body connection and how stress affects the extracellular matrix, which is the support system to all body functions. The role of inflammation and recommendations on how lipedema patients can reduce stress are also reviewed.
June 2, 2021

Decide How Much Living You Want to Do: The Blanche Pepitone Interview

Diagnosed with lymphedema as a baby, Blanche Pepitone had her first surgery at 18 months old. Her parents and siblings raised her to live life fully, regardless of her condition, and that has been Blanche's lifelong credo: "You've got to decide how much living you want to do and do what it takes to live that life."
May 27, 2021

Lipedema Patient Roundtable – May 2021

The May Lipedema Patient Roundtable featured a wide range of topics, including venous ultrasounds and the vein connection to lipedema, the differences between lipedema fat and non-lipedema fat, obesogens and toxins that impact our overall health, and the signs of Ehlers-Danlos.
May 14, 2021

Legs Like Mine: The Susan O’Hara Interview

Lap band surgery resulted in the loss of 171 pounds, but why were her calves still 26 inches each? After the successful weight loss, walking 14 miles a day, and eating a very restrictive diet, she concluded: "This was not just metabolic obesity." Her knees were dislocating 7 - 8 times a day. The social lymphedema communities were a tremendous help to Susan - and then she discovered lipedema.
April 22, 2021

Lipedema Patient Roundtable – April 2021

How chemicals make you fat, managing "usable hours" in a day, pain, heart racing and hot flashes, effective breathing, life after surgery, and lots of encouragement are packed into this one-hour Lipedema Patient Roundtable.
April 20, 2021

Knowledge is Power: The Jenny Beaujean Interview

It took a cat bite that triggered cellulitis at 50 years old for Jenny to finally get a lymphedema diagnosis and another 12 years for an expert to recognize that she also had lipedema.
March 31, 2021

Lipedema Patient Roundtable – March 2021

From lipedema and the COVID vaccine to using heat vs. ice, the March Roundtable was filled with great advice to educate and encourage.
March 8, 2021

Honoring Her Mother by Living Well: The LysaMarie Matamoros Interview

LysaMarie knew something was different about her lower body, but remained undiagnosed for years. Gastric bypass, endless exercise - nothing helped. It was only when she started connecting on Instagram that she saw other bodies like her own, which eventually led to the medical treatment that helped her reclaim her life.
March 8, 2021

Lipedema Patient Roundtable – February 2021

Wisdom, heart, and encouragement are packed into this latest hour of the Lipedema Patient Roundtable brought to you by Lympha Press!
January 22, 2021

Addressing the Epicenter of Lipedema Pain Through Innovative Surgery

An Interview with Dr. Jaime Schwartz of Total Lipedema Care Dr. Jaime Schwartz is a board-certified plastic surgeon and world-renowned lipedema specialist who has dedicated much […]