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Lymphedema Patient Roundtable

Living with lymphedema is challenging. Learn from others with this condition how they effectively manage and thrive while living with lymphedema.

2nd Tuesday of every month
@8:00 PM EST

Lymphedema Patient Roundtable

Learn from the experiences of some of the most insightful influencers in the lipedema world. Bring your questions!

3rd Wednesday of every month
@8:00 PM EST

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4
Mar

Lipedema Patient Roundtable: February 2022

Published: 4 March, 2022

“Having one’s pain and suffering recognized and confirmed is vital, since this creates a power that makes it bearable.” This quote, taken from the 2021 paper Women’s Experiences of Living with Lipedema (Catharina Melander, Päivi Juuso & Malin Olsson), was at the heartbeat of February’s Gal/Palentine’s Day episode.

Our regular panelists brought “plus one’s” like Lympha Press fan (and friend of Brenda) Jenny Beaujean, Pale Ginger Pear‘s friend Kelly Lynn, Cheryl Scoledge‘s friend April Sluder, and a “crossover” appearance by Angela Jones (The Lippy Butterfly‘s guest, who is a regular panelist on our Lymphedema Patient Roundtable).

Dr. Karen Herbst’s pal-entine was Dr. Thomas Wright, another key contributor to The Standard of Care for Lipedema in the United States. Longtime supporter of the lipedema community, Nita Clewis, brought her powerful voice to the conversation, which ran the gamut from moisturizers and supplements, self-love, and excitement surrounding the upcoming FDRS Conference in Cleveland, Ohio.

A heartfelt thank-you to our panelists and guests:

Join the conversation every third Wednesday of the month at 8:00 PM EST! Sign up to attend any of our live webinars at https://linktr.ee/LymphaPress.

The Lipedema Patient Roundtables are brought to you by Lympha Press, makers of the Optimal Plus. The Optimal Plus was specifically designed for lipedema patients, who report results that include reduced pain and increased mobility. Lipolymphedema patients benefit from the movement of lymph that Optimal Plus therapy provides, and often experience reduction in size. Find out more by visiting www.lymphapress.com.

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Lymphedema Patient Roundtable

Living with lymphedema is challenging. Learn from others with this condition how they effectively manage and thrive while living with lymphedema.

2nd Tuesday of every month
@8:00 PM EST

Lymphedema Patient Roundtable

Learn from the experiences of some of the most insightful influencers in the lipedema world. Bring your questions!

3rd Wednesday of every month
@8:00 PM EST

Let's get social!

We’d love to connect with you.

Contact Us.

We're ready to help.

Looking for more information, or to be connected with your local representative?
We can help. Fill out our contact form to get started.