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Support the Endosalpingiosis Foundation

We are a non-profit organization led by women who have been diagnosed with endosalpingiosis. Everything we do is powered by volunteers — from managing our website to representing endosalpingiosis at rare disease events.

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Your donations make a difference. Every dollar you give directly supports our advocacy efforts. Donations help us fund:

  • Supplies for information booths

  • Registration for Rare Disease Week in Washington D.C.

  • Administration fees

  • Fundraiser planning

  • And more!

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With your generosity, we can continue vital programs like the Basket of Hope, which provides support to women around the world. Your contribution, whether it’s $5, $10, or more, ensures we can keep our website and social media channels active, allowing us to reach more people, share critical information, and grow our support network.

 

Together, we can make a difference in the lives of women affected by this rare disease and continue our mission to one day find a cure. Your help has been crucial in getting us this far, and with your continued support, we can accomplish so much more.

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Thank you for standing with us. Let's keep the momentum going!

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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. 

Email: endosalpingiosisfoundation@gmail.com

Phone: (608) 609-5043

Registered Charity: EIN Number: 82-3793988

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© 2022 - 2023 Endosalpingiosis  Foundation. All Rights Reserved.

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