Educational Information & FAQ's on Endometriosis

This EndoRise document has information on the organization, FAQ's on endometriosis along with key stats. 

It's Not Hysteria by Dr. Karen Tang

In It's Not Hysteria, Dr. Karen Tang debunks myths about women’s pelvic pain and reproductive health. Blending medical insight with real stories, the book empowers readers to advocate for better care and understanding.

Endometriosis and Infertility – What You Should Know

This resource explains how endometriosis can impact fertility, outlines diagnostic and treatment options, and provides guidance for those exploring family-building while managing the condition.

Top Questions to Ask After an Endometriosis Diagnosis – Endometriosis Alliance

This guide helps those newly diagnosed with endometriosis navigate next steps by outlining key questions to ask healthcare providers about treatment options, specialist referrals, and long-term management.

Endometriosis Alliance – Advocacy & Awareness

The Endometriosis Alliance connects patients, providers, and advocates to improve education, advance research, and promote policy change around endometriosis care and awareness.

Nancy’s Nook – Endometriosis Education & Support

Nancy’s Nook is an educational platform offering evidence-based information on endometriosis, expert-recommended specialists, and a supportive community for patients seeking accurate diagnosis and treatment.

Pelvic Health Fund

For the general patient population:

Pelvic Health Fund is a nonprofit with the mission of providing pelvic health tools such as vaginal dilators, pelvic wands, and support belts to those with financial barriers. If the cost of the pelvic products your provider has recommended is simply too high for you to afford, please consider applying for support. If you are not yet seeing a pelvic floor specialist and would like help finding qualified providers, reach out through our Contact Us page and we would be happy to help you find someone in your area.

CDC Archive: Talking to Family About Your BRCA Gene Mutation

This CDC guide offers tips for discussing BRCA1 or BRCA2 gene mutations with family. It explains why sharing this information matters, who may be at risk, and how to navigate these important conversations with support and clarity.

CDC Archive: 2024 Quality Family Planning (QFP) Recommendations

This overview from the U.S. Office of Population Affairs outlines the revised 2024 QFP recommendations, which set new standards for inclusive, person-centered sexual and reproductive health care. It emphasizes equity, trauma-informed approaches, and expanded access to services like contraception, STI prevention, family-building, and early pregnancy care. The update includes 10 core recommendations designed to improve SRH outcomes and reduce health disparities across diverse care settings.

CDC Archive: Providing Quality Family Planning Services

This revised 2024 guidance from the CDC and Office of Population Affairs outlines best practices for delivering equitable, person-centered family planning services. It supports providers in offering inclusive care that reflects patient preferences, updated clinical standards, and broader access options like telehealth.