I am a passionate lipedema patient awareness advocate who has spent decades struggling with unexplained symptoms and “normal” test results before being diagnosed with the condition in 2020. Since my diagnosis, I have been committed to researching and understanding lipedema to better manage my symptoms, as well as helping others avoid the same struggles I’ve faced.
I share my personal stories and practical advice to inspire others who are living with lipedema. I believe that through education, advocacy, and support, patients can improve their quality of life and prevent unnecessary suffering. With my expertise and passion, I hope to positively impact the lives of those living with lipedema and contribute to a more supportive and understanding healthcare system.