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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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28
Dec

Lipedema Patient Roundtable: December 2023

Published: 28 December, 2023

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 fielded a host of questions, from hormones and hair loss to prescriptions and pumping, while Sonya Louise, a coach who helps women with chronic illness navigate life, offered tactics for managing pain and finding purpose. “Placing your awareness on what doesn’t hurt” was a powerful takeaway for the audience, and questions like “What signals that lipedema is progressing?” were also discussed.

New visitors to the Roundtable audience were welcomed with open hearts. One attendee had just received their diagnosis that day and asked, “What would be the first thing you’d do if you were me?” The answers included downloading ⁠the Standard of Care for Lipedema in the US⁠, finding a knowledgeable therapist, and “finding your people.”

Special thanks go to anchor panelists, moderator, and amazing guests:

Lympha Press supports the lipedema community by sponsoring these monthly Roundtables and ⁠welcomes inquiries⁠ about their easy-to-use pneumatic compression therapy. Lympha Press representatives can connect patients with knowledgeable doctors and therapists around the country, fulfilling the company’s mission to offer therapy that’s easy to live with. Visit ⁠www.lymphapress.com⁠ to find out more.

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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.