EndoRISE
EndoRISE
A community to advance Endometriosis Research, Innovation, Support & Education

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EndoRISE is a groundbreaking, state supported initiative to address Endometriosis, a highly invasive, under-diagnosed and under-researched disease.
Seeking to improve awareness and health outcomes in Connecticut, while driving research breakthroughs that will impact women across the nation and beyond, the EndoRISE program's multifaceted approach includes:
  • The creation of the CT Data and Biorepository, a diverse data and specimen biorepository to enable research, clinical and industry collaborations
  • The education of healthcare providers, students and frontline professionals about endometriosis diagnosis and best practices
  • Serving as a centralized resource, to disseminate information and raise public awareness about the disease
Whether a patient, researcher, provider, or simply interested in learning more, we welcome you to join us in the effort to impact the lives of the over 200 million people suffering from this disease.

Public

Learn more about Endometriosis, who it effects, and the importance of raising awareness of the disease for early detection and advancements in health outcomes for those suffering from it.

Patients

Find information, resources and community. Learn more about how you can help advance EndoRISE efforts towards better diagnostics, treatments and cures.

Researchers

Learn more about the CT Data and Biorepository and its efforts to foster basic research and clinical collaborations designed to help advance our understanding of Endometriosis towards better diagnostics, treatments and cures.

Providers

Learn more about Endometriosis, best practices in patient care, and the role you can play the effort to advance diagnostics, treatments and cures.
Recent News
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November 07, 2025
What happens when we start telling the truth about women’s pain?

Dr. Danielle Luciano, OB-GYN and Co-Director of EndoRISE, sits down with Isabel from Sober Spill to talk about the real story behind endometriosis: the mental and physical weight, the years of being unheard, and the movement toward change. From breaking the silence on chronic pain to reshaping women’s healthcare through research and advocacy, this conversation is a powerful reminder that healing begins with being seen and believed.

Watch here
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August 21, 2025
Dr. Katie Burns, a pathobiologist and toxicologist at the University of Cincinnati (UC) was featured in Science Magazine on her mission to uncover the role of the immune system in endometriosis—while managing the disease herself.

Read more
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Upcoming and recent events
  • Virtual Convention:  All Nurses Across All Specialty Areas: Raising Awareness About Endometriosis
    Virtual Convention: All Nurses Across All Specialty Areas: Raising Awareness About Endometriosis
    · March 20, 2025
    EndoRISE is partnering with the Connecticut Nurses Association to offer a professional development session on endometriosis and the EndoRISE program to the nursing community across the state of Connecticut

    March 20th, 2025 • 5:30 - 6:30pm
    It may take 7 years to diagnose endometriosis! We will discuss recognizing the signs and symptoms of endometriosis, and explore educational materials for health professionals and to support patients.
    *School Nurses
    *ER/Urgent Care/Primary Care
    *APRNs

    Register by clicking "Learn More"
  • Screening of "Below the Belt" documentary
    Screening of "Below the Belt" documentary
    · April 10, 2025
    EndoRISE and the University of Connecticut PNB society bring you a special screening of "Below the Belt", a documentary on endometriosis and flaws in the healthcare system.
  • 2025 EndoRISE Fall Forum
    2025 EndoRISE Fall Forum
    · December 08, 2025
    2025 EndoRISE Fall Forum December 8, 2025 Free event, available both in person and online
Contact Us
For more information on EndoRISE or the biorepository, please complete the form below to get in touch with someone from the program. Click here to request samples.
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