Image by NASA

Contribute to the future of Endosalpingiosis Research

Help bring patients, families & researchers together to gain a better understanding of Endosalpingiosis!
Image by NASA

Contribute to the future of Endosalpingiosis Research

Help bring patients, families & researchers together to gain a better understanding of Endosalpingiosis!
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our

mission

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!

 Endosalpingiosis is a painful reproductive condition where tissue from the fallopian tubes are found outside the tubes, and elsewhere in the pelvic cavity, causing pain and infertility. 

Common symptoms include pelvic pain, pain between periods, painful sex, dyspareunia, back pain, mood swings and problems sleeping. 

There is no known cure for this disease.

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