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The Lympha Press Podcast

Lympha Press

The Lympha Press Podcast

A weekly Health and Fitness podcast
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The Lympha Press Podcast

Lympha Press

The Lympha Press Podcast

Episodes
The Lympha Press Podcast

Lympha Press

The Lympha Press Podcast

A weekly Health and Fitness podcast
Good podcast? Give it some love!
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Episodes of The Lympha Press Podcast

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For the lipedema community, the Fat Disorders Resource Society (FDRS) Conference is an annual highlight. At the April Lipedema Patient Roundtable, host Brenda Viola and Angelique Charles “zoomed” from St. Louis Missouri, where the next few days
Spring has sprung, and the April Lymphedema Patient Roundtable was blooming with conversation around themes of community and support! Special guest Veronica Seneriz from the Lymphatic Education and Research Network walked attendees through LE&R
Oh, the places you will go with lymphedema and lipedema! Karen Ashforth, MS, OTR, CLT-LANA, and a panel of expert patient travelers (Amy Rivera, Catherine Rosenberg, Angela Jones, and Alexa Ercolano) discuss the ins and outs of preparing to tra
"Perfectionism is the enemy of good." This was just one of the powerful takeaways from the March Lipedema Patient Roundtable. Special guest Dr. Nicholas Pennings, DO, FOMA, FACO, FP, has devoted his career to studying and treating obesity and l
Happy Lymphedema Awareness Month! Every month is Lymphedema Awareness Month at the Lymphedema Patient Roundtable, but even more so in March.What does "lymphedema awareness" mean to you? And what about the butterfly, the symbol for lymphedema?
John Chuback, MD, FACS, discusses the cardiovascular system, particularly how the heart is central to the magnificent anatomical and physiological network of arteries, veins, and lymphatic vessels.During this conversation with Lympha Press Pre
Love is always in the air at the Lipedema Patient Roundtable, but the feeling was palpable as the group shared what community means to them in this “Galentines” episode. With representatives from the Lipedema Foundation and Fat Disorders Resour
From navigating relationships with lymphedema to the way loved ones support us in our lymphedema lives, to how we show ourselves and our lymphedema some love (even when it’s difficult to do so) – the Lymphedema Patient Roundtable had a lot to d
Compression, compression, compression! The main flow of conversation revolved around this all-important component of lipedema (and lymphedema) management. Cara Cruz’s own certified lymphedema therapist, Megan Glod, joined the panel as a special
Happy New Year! The Lymphedema Patient Roundtable kicked off 2024 with a robust conversation around lymphedema management, including complete decongestive therapy, wraps and bandages, and pneumatic compression pumps. A few folks in the chat eve
The spirit of the season was evident at the December Lipedema Patient Roundtable, and the gifts of encouragement and insight were plentiful.Two special guests made the hour extra special: ⁠Lympha Press Chief Medical Officer Dr. Karen Herbst⁠ f
Merry Lymphmas from the December Lymphedema Patient Roundtable! The holidays can sometimes be a difficult time, not just in managing our lymphedema but navigating the mental or emotional pangs of the season as well. The panel talked about some
Can you imagine not being able to go to the dentist because the patient chair is unsuitable for anyone over 300 pounds? Or having an aversion to calling an ambulance because you feel it’s too embarrassing to be placed on the gurney?The challen
The Lymphedema Patient Roundtable was bursting with “lymphatic gratitude” this month as the regular panel was joined by special guest Jasmine Zheng, MD, CLT, FAAPMR, from Penn Medicine!What are central lymphatic issues? How might they present?
It was a boo-tiful night to talk about lipedema, especially since Linda Anne Kahn had recently returned from the Lipedema World Congress in Germany, filled with insights and emerging research to share! Special guest Dr. Molly Sleigh also joined
With it being Breast Cancer Awareness Month and the Roundtable falling on both World Mental Health Day and World Metabolic Health Day, there was much to discuss at the October Lymphedema Patient Roundtable!To top it off, a number of our paneli
Named the President of the Save a Leg, Save a Life Foundation (SALSAL) in 2022, Frank Aviles is passionate about the early diagnosis and treatment of wounds: “People don’t realize that they should treat a wound just as they would a cancer diagn
September is Pain Awareness Month, and the anchors and attendees of the Lipedema Patient Roundtable know all too well the aching associated with their condition. The remarkable improvements Cara Cruz has achieved through surgery and the many pa
Class is officially in session at the September Lymphedema Patient Roundtable, and the syllabus covered everything from finding a support system and staying encouraged while managing lymphedema, to an interesting conversation on the Perrin Tech
Driven by curiosity her entire life, Karen Herbst was fascinated with the idea of fat since childhood: Where does it come from? How could some people live on a diet of fruits and vegetables and yet have disproportionate fat deposits? Her academ
This episode of the Lipedema Patient Roundtable was as hot as the month of August! Our anchor panelists have made waves since we last gathered: The Lippy Butterfly, Angelique Charles, discussed the amazing article she authored about lipedema on
The panelists changed things up at the August Lymphedema Patient Roundtable by introducing a new format featuring a panelist chat and a Q&A open forum followed by the first-ever “Lymphedema Patient Roundtable Call-in Show”!Did you know we have
This interview was recorded in June 2021. "I was so grateful to learn that there was such a thing as lipedema." At one point, Francine Schwartz was 425 pounds. Doctor after doctor just told her to "lose the weight." Peri-menopause exacerbated
Two new hashtags were birthed following the July Lipedema Patient Roundtable's riveting discussion: #DoTheThing and #WearTheThing were shared by Pattie Cornute and Pale Ginger Pear. The message? Don't talk yourself out of trying something new f
It’s summertime and a lot of people are going on vacation, but as we all know: lymphedema does not take a break. Whether going down the shore or traveling across the globe, the panelists and attendees at the July Lymphedema Patient Roundtable s
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