Who IS THE AMERICAN LIPEDEMA ASSOCIATION?

The American Lipedema Association is a 501(c)(3) nonprofit organization dedicated to empowering lipedema patients in the United States. We are a community of individuals affected by lipedema, along with medical professionals, researchers, and advocates, united in raising awareness and understanding of this underdiagnosed loose connective tissue disorder.

Our mission is to provide support, resources, and a collective voice for those impacted by lipedema, while promoting research efforts to advance treatment options and improve quality of life.

Together, we strive to foster a compassionate environment where lipedema patients feel heard, validated, and empowered on their journey.

This June 5th the ALA is presenting their first All or Something The Pattie Cornute Award to someone who reflects Pattie’s legacy in action.

Nominate someone here

Criteria for the award include:

– The candidate must be a patient, living with lipedema
– The candidate cannot be a current board member of the American Lipedema Association
– They must show a consistent effort towards wellbeing, demonstrating resilience
and persistence
– They should demonstrate selfless support and encourage others, helping others to feel
less alone in their journeys
– They must demonstrate self-compassion in their own journey
– They must honor small steps, especially and even on hard days

Nominations are open until May 15th at 11:59 PM Central Time.

This award is made possible through the generous support of LymphaPress , whose commitment has helped bring this recognition to life. (However, LymphaPress is not a part of the awardee selection process.)