A Whirlwind Week! In a GREAT Way! Travel, and Shoes and Education Groups. Oh My!

Wow ya’ll! I’ve spent the last week working away at so many things (in addition to my paying job) for lipedema.  I feel that 2022 is the year that we’re making a giant leap in research, awareness, and serving the sometimes looked-over community with lipedema. I’ve just posted about my involvement with the Lipedema EducationContinue reading “A Whirlwind Week! In a GREAT Way! Travel, and Shoes and Education Groups. Oh My!”

Celebrating the Medical Professionals Who are Dedicated to Making Lipedema Patient Lives Better

Hi friends, If you follow many of the facebook support groups for women with lipedema, you’ve probably seen a new movement in our ranks:  We are doing writing campaigns to educate doctors and clinicians who have not responded well to our requests to diagnose or discuss lipedema.  In the first weeks alone, I completely depletedContinue reading “Celebrating the Medical Professionals Who are Dedicated to Making Lipedema Patient Lives Better”