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Miss Lippy (Michelle) has been on a lifelong journey with her lipedema since adolescence. Now in her 50s, it took 34 years to get a diagnosis in another 20 to get therapy. She’s here to tell her story of her journey and this under-appreciated, under diagnosed and typically mistreated condition. Her goal, like ours at Lily Clinic, is to raise awareness to decrease the suffering of the next generation!

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Laura Chevreaux is a LANA Certified Lymphedema Therapist and Wound Therapist who recently opened up her own clinic, The Swell Spot, in St. George, Utah. She shares her experience as a therapist at Brylan's Feat Foundation's Camp WatchMe. Camp WatchMe is a summer camp for children with lymphedema, their parents, and therapists.

Please consider donating to www.brylansfeat.org to support this incredible cause.

For more information on Laura and the great work she is doing check her out here: https://www.facebook.com/theswellspotstg

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In this part 3 of 3 podcast, we conclude our discussion with Kelley about her amazing journey from acquiring lymphedema to fighting the insurance companies and getting surgeries to where she is now. What is her life like now. What is her lymphedema like now. Have things improved?