(Lipedema) These Legs Must Dance: The Beth McKee Elliott Interview

“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 was recorded in July 2020. You can watch the video recording of Beth's interview on the Lipedema Channel on YouTube, or on Instagram at @lympha_press. The Lipedema Channel interviews are brought to you by Lympha Press, global leaders in pneumatic compression therapy for nearly 40 years. For more information, visit lymphapress.com.