Our mission is to spread awareness and educate our community for Endosalpingiosis, a rare disease that exclusively affects people born with a uterus. While our aim will always be to find a cure, we hope to engage the academic and scientific community in search of a therapeutic treatment to treat this devastating condition. We host awareness campaigns online to help bring awareness and raise funds to support the needs of our community, in addition to hosing the Endosalpingiosis Registry to support the advancement of research and development.
No matter where you live, we are need to come together globally to bring awareness about this disease to everyone. We are educating our doctors, family, friends and anyone else that wants to learn about this disease.
You aren't alone in fighting this disease!