You deserve a diagnosis,
not a diet.

One patient’s journey through lipedema diagnosis, surgery, and the fight to be believed, with a focus on the arm representation that medicine keeps missing.

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Hi, I Am Kelly Schwartz

I live with Lipedema.

I was diagnosed in August 2025 and had my first surgery just seven months later… seven months of fighting insurance, advocating for myself, and documenting every step for all the women who spent years blaming their bodies for something that was never their fault. This site is where my story lives.

01

Half-Marathon Runner

Wore compression for years without knowing why.

02

A Facebook comment changed my life.

That’s how I found out I had lipedema.

03

Single mom, Wisconsin-raised, big dog person.

House fire survivor. Still standing.

04

Marketing director turned patient advocate.

I know how to tell a story — and yours deserves to be told.

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