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Interviews

Every person's story is worth telling.

There is no definitive lymphedema or lipedema experience.

From veterans and athletes to college students and parents, life with these conditions is as varied as the people who live with them. Hear from real patients as they share their stories, in their own words.

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7
Aug

These Legs Must Dance: The Beth McKee Elliott Interview

Published: 7 August, 2020

“To not be able to move as a dancer is to not remember who you were,” shared Beth McKee Elliott. This moving interview about her lipedema journey offers hope to other women with mobility challenges. A cortisol cascade changed her body dramatically and for years she went undiagnosed. She now says, “My legs look like old friends.”

Find out about what she’s learned about self-acceptance through her somatic practice, her decision to have surgeries, and her message of hope to those who have (or think they have) lipedema.

This interview is part of a series brought to you by Medical Solutions Supplier, exclusive providers of Lympha Press. Lympha Press offers an FDA cleared pneumatic compression device for the treatment of lipedema. To learn how the Optimal Plus can help you, e-mail bviola@medsolsupplier.com.

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