Lipedema Manitoba Association is the only dedicated organization in Manitoba supporting individuals affected by lipedema—a chronic and often misunderstood condition that primarily affects women. Lipedema is a progressive disorder characterized by the abnormal accumulation of fat, typically in the legs and arms, leading to pain, swelling, and mobility challenges. Despite its prevalence, lipedema remains widely underdiagnosed and frequently mistaken for obesity or lymphedema.

Founded in 2023, Lipedema Manitoba Association is a registered not-for-profit and charitable organization committed to improving the lives of those living with lipedema. Our mission is to increase awareness, educate the public, healthcare professionals, and policymakers, and advocate for better care and support.

Through direct support programs, we strive to make a meaningful difference in the lives of lipedema patients. Our initiatives include:

Compression funding assistance to help those in financial need with essential medical garments.Community events that provide education and connection for those affected.Inclusive exercise classes designed to support movement and well-being such as lipedema yoga and aquafit.

Recognizing the significant gaps in understanding and treatment, Lipedema Manitoba collaborates with Lipedema Canada, our national partner, to advance research, advocacy, and education efforts. Together, we work tirelessly to ensure that lipedema is better recognized, diagnosed earlier, and managed effectively.

Whether you are living with lipedema, supporting a loved one, or a professional seeking knowledge, Lipedema Manitoba is here to help.