I Think I Have Lipedema. And I Have Questions! Talking w/ Lipedema Newbie Lisa Foster

Today we are talking with someone who is brand new to the world of Lipedema, self-diagnosed and looking for an official diagnosis and asking all the questions- Lisa opens up today and turns the tables. She's asking US the questions. Listen as she asks so many of the questions that we all wondered about when we first found out about Lipedema. This will be the episode to send to your friends who are newbies too.

If you are like Lisa and new to this world and looking for community, reach out to her on Instagram @lisajanekc

You can find Shawn on Instagram at @the_lipedema_mama

You can find Ashley on Instagram at @the_lippy_lady

Thank you, as always, to our sponsors: Lipoelastic and AIROS Medical and Arion Slides.

For more information on Lipoelastic, go to www.lipoelasticshop.com and their Instagram @lipoelastic_usa

For 10% off your purchase in the UK or US, enter the code LIPEDEMAMAMAS

For more information on the pneumatic compression devices from AIROS Medical, visit www.airosmedical.com/lipedemamamas

To purchase Arion slides, visit www.compressionguru.com

New to the Lipedema world? At a loss for what to do? Not sure how to start managing this disease conservatively? Check out www.lipedemacourses.com

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