Endometriosis is a chronic, often painful condition where tissue similar to the lining of the uterus grows outside the uterus—on the ovaries, fallopian tubes, pelvic lining, and sometimes even beyond. This tissue responds to hormonal changes, leading to inflammation, scarring, and severe pain.
Despite affecting roughly 1 in 10 women of reproductive age worldwide, endometriosis has historically been misunderstood, underdiagnosed, and mistreated.
World Health Organization Fact Sheet on Endometriosis:
https://www.who.int/news-room/fact-sheets/detail/endometriosis

That’s not a typo. On average, it takes 7 to 10 years from the first symptoms to a correct diagnosis. Why?
• Symptoms are often normalized: Severe period pain? “Just part of being a woman.”
• Lack of non-invasive testing: Diagnosis has long relied on laparoscopic surgery.
• Medical gaps: Many healthcare providers, including OB-GYN’s, receive limited training in gynecologic pain conditions.
NIH: Delays in Endometriosis Diagnosis: https://pubmed.ncbi.nlm.nih.gov/32147966/

Every woman’s experience is different, but some of the most common symptoms include:
• Intense pelvic or abdominal pain
• Pain during or after sex
• Heavy or irregular periods
• Chronic fatigue
• Gastrointestinal issues like bloating, nausea, or constipation
• Infertility or difficulty conceiving
New Diagnostic Tools
• MicroRNA panels and blood-based biomarkers are showing promise as non-invasive ways to detect endometriosis earlier.
• Advanced imaging like high-resolution MRI and ultrasound with specialized protocols are helping detect lesions more reliably.
Endometriosis Foundation: Emerging Research: https://www.endofound.org/news-research
PubMed: Biomarkers in Endometriosis: https://pubmed.ncbi.nlm.nih.gov/30807918/
AI & Machine Learning
Artificial intelligence is being trained to analyze symptom patterns, scan images, and even detect potential markers in menstrual blood—offering hope for faster, more accurate screening in the near future.
More Funding and Advocacy
• Governments and nonprofits are increasing research grants.
• Social media and support groups are amplifying women’s voices and experiences.
• Healthcare providers are receiving more training in pelvic pain and minimally invasive surgical options like excision surgery.

Faster, less invasive diagnosis is on the horizon.
Women are being believed and supported more than ever.
With better understanding comes more targeted treatment options, like hormonal therapies, dietary approaches, pelvic floor therapy, and expert excision surgery.
1. Track your symptoms: Keep a daily journal of pain, mood, fatigue, and cycle details.
2. Advocate for yourself: Ask your doctor about excision surgery vs. ablation. A specialist is necessary for proper endometriosis care. Unfortunately, your typical OB-GYN is not an endometriosis or excision specialist.
3. Get support: You're not alone. Online communities and advocacy organizations offer connection and practical help.
Nancy’s Nook Endometriosis Education Group: https://www.facebook.com/groups/NancysNookEndoEd
Center for Endometriosis Care: https://www.centerforendo.com/
Endometriosis is a whole-body disease that can affect a woman’s physical, emotional, and reproductive health. We are just starting to make some noise & bring attention to this disease and other hormonal diseases related to it.
Endometriosis is a chronic, often painful condition where tissue similar to the lining of the uterus grows outside the uterus—on the ovaries, fallopian tubes, pelvic lining, and sometimes even beyond. This tissue responds to hormonal changes, leading to inflammation, scarring, and severe pain.
Despite affecting roughly 1 in 10 women of reproductive age worldwide, endometriosis has historically been misunderstood, underdiagnosed, and mistreated.
World Health Organization Fact Sheet on Endometriosis:
https://www.who.int/news-room/fact-sheets/detail/endometriosis

That’s not a typo. On average, it takes 7 to 10 years from the first symptoms to a correct diagnosis. Why?
• Symptoms are often normalized: Severe period pain? “Just part of being a woman.”
• Lack of non-invasive testing: Diagnosis has long relied on laparoscopic surgery.
• Medical gaps: Many healthcare providers, including OB-GYN’s, receive limited training in gynecologic pain conditions.
NIH: Delays in Endometriosis Diagnosis: https://pubmed.ncbi.nlm.nih.gov/32147966/

Every woman’s experience is different, but some of the most common symptoms include:
• Intense pelvic or abdominal pain
• Pain during or after sex
• Heavy or irregular periods
• Chronic fatigue
• Gastrointestinal issues like bloating, nausea, or constipation
• Infertility or difficulty conceiving
New Diagnostic Tools
• MicroRNA panels and blood-based biomarkers are showing promise as non-invasive ways to detect endometriosis earlier.
• Advanced imaging like high-resolution MRI and ultrasound with specialized protocols are helping detect lesions more reliably.
Endometriosis Foundation: Emerging Research: https://www.endofound.org/news-research
PubMed: Biomarkers in Endometriosis: https://pubmed.ncbi.nlm.nih.gov/30807918/
AI & Machine Learning
Artificial intelligence is being trained to analyze symptom patterns, scan images, and even detect potential markers in menstrual blood—offering hope for faster, more accurate screening in the near future.
More Funding and Advocacy
• Governments and nonprofits are increasing research grants.
• Social media and support groups are amplifying women’s voices and experiences.
• Healthcare providers are receiving more training in pelvic pain and minimally invasive surgical options like excision surgery.

Faster, less invasive diagnosis is on the horizon.
Women are being believed and supported more than ever.
With better understanding comes more targeted treatment options, like hormonal therapies, dietary approaches, pelvic floor therapy, and expert excision surgery.
1. Track your symptoms: Keep a daily journal of pain, mood, fatigue, and cycle details.
2. Advocate for yourself: Ask your doctor about excision surgery vs. ablation. A specialist is necessary for proper endometriosis care. Unfortunately, your typical OB-GYN is not an endometriosis or excision specialist.
3. Get support: You're not alone. Online communities and advocacy organizations offer connection and practical help.
Nancy’s Nook Endometriosis Education Group: https://www.facebook.com/groups/NancysNookEndoEd
Center for Endometriosis Care: https://www.centerforendo.com/
Endometriosis is a whole-body disease that can affect a woman’s physical, emotional, and reproductive health. We are just starting to make some noise & bring attention to this disease and other hormonal diseases related to it.
Your support can transform lives. Every donation helps us fund research, advocate for better care, and provide essential grants to women facing debilitating conditions.
Your support can transform lives. Every donation helps us fund research, advocate for better care, and provide essential grants to women facing debilitating conditions.


Hope on the Horizon: Breakthroughs in Endometriosis Research
Living with endometriosis or PCOS or fibroids (or any of the other hormone related, immune system diseases) can feel isolating, frustrating, and hopeless, especially for women who are actively fighting symptoms. We have previously highlighted the delay, dismissal and pain that is part of the experience for many of these women. BUT we also want to bring hope by saying that the landscape is starting to shift. Across the globe, researchers are unlocking new discoveries, philanthropists are investing boldly in women’s health, and for the first time in decades, there’s momentum toward real change. We hope this fills you with HOPE today and helps you to know that you are seen and cared for!
Here’s a look at some of the most hopeful developments reshaping the future of endometriosis care — and why we’re optimistic. (AND why we are doing our own research to know the best and most impactful places to invest our dollars!)
New Science Lighting the Way
Moving beyond hormones and surgery
Most current endometriosis treatments rely on hormonal suppression or invasive surgery — options that often come with serious side effects and don’t prevent recurrence or offer a cure.
But a new wave of research is aiming to change that.
Dichloroacetate (DCA), a metabolic drug once used for mitochondrial disorders, is showing surprising promise. In early clinical trials, it reduced lesion size and eased pain in many participants.
“This is the first time we’ve seen a drug target the energy metabolism of endometriosis cells. It’s a potential game-changer,”
— Professor Andrew Horne, University of Edinburgh
HMI-115, a monoclonal antibody targeting the prolactin receptor, is showing significant reductions in pain in Phase II trials.
“The fact that it’s non-hormonal and well tolerated could transform quality of life for millions,”
— Dr. Thomas D’Hooghe, Global Head of Reproductive Medicine R&D at Merck
More than 20 novel therapies are in development, many focused on immune and inflammatory pathways rather than hormones alone. This could lead to disease-modifying treatments, not just symptom control.
Faster, earlier diagnosis
Delays of 7–10 years from symptom onset to diagnosis are still common. That may soon change.
Big-data work at UCSF has identified patterns in millions of health records that could flag endometriosis earlier.
“We’re using artificial intelligence to see what no single doctor could spot in a lifetime,”
— Dr. Marina Sirota, UCSF Institute for Computational Health Sciences
In Australia, researchers are testing a blood-based biomarker panel that could detect endometriosis non-invasively.
New AI-assisted MRI tools are learning to identify endometriosis lesions with accuracy that rivals expert radiologists.
Dedicated research hubs
In May 2025, the Seckin Endometriosis Research Center opened at Cold Spring Harbor Laboratory, powered by a $10 million gift from the Endometriosis Foundation of America (EndoFound) and matched with another $10 million in institutional funding.
“We are building the infrastructure that has been missing in this field for decades. This is how you accelerate cures,”
— Dr. Bruce Stillman, President, Cold Spring Harbor Laboratory
Philanthropy Is Fueling Breakthroughs
After decades of neglect, private donors are helping rewrite the story of women’s health.
The Bill & Melinda Gates Foundation has pledged $2.5 billion through 2030 toward R&D in women’s health, explicitly including gynecologic conditions like endometriosis.
WHAM (Women’s Health Access Matters) has launched its annual Edge Awards to fund early-career researchers focused on endometriosis, PCOS, and menopause.
The Ainsworth family in Australia donated $50 million to launch the Ainsworth Endometriosis Research Institute at the University of New South Wales — the largest known single gift for endometriosis research to date, with the goal of accelerating the understanding, diagnosis and treatment of endometriosis through “integrated research and global collaboration.”
Melinda Gates donated $100 Million to women’s health in order to accelerate research. She emphasized what so many of us have known and live with the consequences of: women’s diseases have been neglected.
This surge in philanthropy is helping fill the gap where public funding has long fallen short. And the list above is not complete, there are many smaller efforts (like Our Daughters Foundation) that seek to fund research, grants for care, and raise awareness.
“Private investment is finally catching up to the urgency patients have always felt. These dollars are helping researchers pursue the bold, risky ideas that government grants often overlook,”
— Dr. Stacey Missmer, Harvard T.H. Chan School of Public Health
Stories of Hope
Beyond the data and dollars, these breakthroughs are already changing lives.
Ella, diagnosed at 14, was one of the youngest participants in the EPiC DCA trial. After years of missing school and friends, she finally began to get her life back.
“It’s like someone turned the volume down on my pain. I can go to class, see friends, be me again.”
Marisol, who endured five surgeries before finding relief with a newer oral therapy, says:
“For the first time in years, I’m planning my future without fear that pain will ruin it.”
We have also featured stories of hope on our pages to show you that you are not alone in your suffering and we are getting closer to understanding this disease.
🌱 Why We’re Hopeful
Endometriosis research is moving from a trickle to a tide, it’s a slow tide and we have a ways to go, but we are moving in the right direction. More of us are making noise, advocating and giving so that we can make a difference now and for our daughters in the future.
New, non-hormonal therapies are emerging.
Faster, less invasive diagnostics are within reach.
Philanthropy and private investment are pouring unprecedented resources into this space.
And most importantly, patients’ voices are finally driving the agenda.
At Our Daughters Foundation, we believe this momentum is just the beginning. The more we invest in understanding this disease — from immune pathways to diagnostic tools — the faster we can build a future where girls and women no longer lose years to pain. It’s a great time to get involved and actually see positive outcomes!
Join the Momentum
Every gift matters. Every conversation matters.
Together, we can help ensure this moment becomes a movement — and that every daughter has a future free from these often debilitating conditions and diseases.