The Endometriosis Association stands as a pivotal self-help organization that plays a crucial role in the lives of individuals affected by endometriosis—a complex and often misunderstood disease. This organization brings together a diverse community consisting of women suffering from the disease, their families, healthcare professionals, scientists, and other individuals who share a common interest in understanding and combating endometriosis. By fostering an environment of support and information exchange, the Association empowers its members and contributes significantly to both individual well-being and the broader scientific understanding of the disease.
Founded with the purpose of offering support, education, and advocacy, the Endometriosis Association is headquartered in Milwaukee, Wisconsin, in the United States, but its reach and impact are global. Members from numerous countries across different continents are part of this dynamic network, actively participating in various programs and activities organized by the Association. This international presence not only amplifies the range of experiences and knowledge shared but also enhances the global dialogue on endometriosis, leading to more innovative and inclusive approaches to its management and treatment.
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