It’s not just reproductive. It’s systemic. We need better care, more research, and greater awareness. Link to the study findings:

New research confirms what many #endo patients have long known: #endometriosis is linked to increased risk of autoimmune + inflammatory diseases—including RA, MS, coeliac, and more.

Rachel had no symptoms—until stage IV endo turned her world upside down. Years of misdiagnosis, fertility struggles, and finally, healing. Her story is a reminder: silent #endometriosis is real, and you’re not alone. 💛  

Policy change is possible. Your voice matters. Join us @endofound & be part of the movement: #endometriosisawareness #endoadvocacy

💛 Hope is rising for #Endometriosis care. MA just introduced its first-ever endo bill—joining states like CT, NY & NJ that have already taken action.

New EndoTV: Dr. Chu shares why connection is just as important as treatment. From preparing for consults to navigating surgery decisions, she emphasizes how support—medical and emotional—can help you feel less alone. Watch here: @dianafalzone

RT @DrSeckin: Dr. Tamer Seckin responds from the boat: "Why does endometriosis get worse in the summer heat?"💬. Discover how endometriosis….

Swipe through for gentle, judgment-free guidance. And if you’ve found what works for you, tweet us—we’re in this together.

Exercising with #endometriosis? It’s complicated. 💛 Some days, movement feels empowering. Other days, even stretching feels impossible. This carousel shares real tips from an #endowarrior who’s learned to navigate fitness on her own terms—without guilt.

In her new @people interview, Julianne opens up about the emotional decision to freeze her eggs for a third time, and how she’s approaching this phase of life and career with intention and self-awareness:

.@juliannehough has been an outspoken advocate for #endo awareness for years, helping to break the silence around a condition so many live with. Thank you, Julianne, for your continued honesty—and for using your voice to empower others in the #endometriosis community & beyond

#Endometriosis affects #1in10,  but it’s still underdiagnosed, misunderstood, underfunded. That’s why we launched One for the Cure: to raise $1M to fund one year of research. This July, we're asking you to stand for freedom from pain, silence & delay:

RT @DrSeckin: If you’re struggling with painful intimacy, it could be due to endometriosis. Learn the signs, causes, and how to get help. Y….

Spark change this #4thofjuly. Not with fireworks but with action. Give $1 to help fund one year of #endometriosis research. Every dollar gets us closer to a cure. Be One for Freedom. Make your contribution here:

At 21, Lucy Metheny has faced migraines, TB, and years of #endo pain—only to be told her disease was ‘mild.’ One lesion changed everything. Her message? Pain is real, no matter the stage. And it deserves to be heard. 💛.

This July 4, we’re not just celebrating freedom — we’re fighting for it. 1 in 10 live with #endometriosis, often in silence and without answers. We’re raising $1 million to fund one full year of research to change that. Give $1. Be One for Freedom:

Help us change the future of #endo—one classroom at a time.💛. Volunteer with EndoFound’s ENPOWR Project to bring menstrual health + #endometriosis education to high school students. Sign up:

The Blossom Ball red carpet was full of powerful voices & heartfelt moments — this one truly stood out. @thefolake shared what bringing awareness to #endometriosis does, and why events like Blossom Ball are much more than just a night out, but an opportunity to fight for change

EndoFound’s first ENPOWR College Ambassador pilot program made waves:.🏫 20 campuses.🎓 21 ambassadors.📣 18 events.👥 934 students reached.📚 5K materials shared.We’re now recruiting for 2025–2026!.Passionate about #endo awareness? Join us:

What are some of your go-to songs? Let’s build the ultimate #endowarrior playlist together.