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Empowering Lipedema Patients Through Advocacy Empowering Lipedema Patients Through Advocacy ALA Home Who We Are The American Lipedema Association is a 501c3 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.