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Contribute to the future of Endosalpingiosis Research

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


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!

March 2021

Endosal New Member Victoria Jackson
You can download the application below

This nonprofit organization was founded with the mission of raising awareness for Endosalpingiosis, a rare disease that exclusively affects women. Endosalpingiosis Foundation Inc. vows to advocate and help the women impacted by this devastating rare disease through events and community support programs. 


Phone: (608) 609-5043

Registered Charity: 12345-67

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