Stories. Vetted specialists. A community that already understands. Tools that help you advocate for yourself — in English and Spanish, from day one.
The Endo Project is a global, bilingual home for the 190 million women and girls living with endometriosis. A place to find language for what you're going through, people who already understand, and practitioners worth your time.
For sixteen years I was told my pain was normal. I built this because no one else should have to learn what I learned alone.
Seven things, made carefully. Free where it matters. Premium where it must be.
A long-form, mixed-media account of one woman's path through the disease — and the founding ground for everything else.
A vetted, global index of endometriosis specialists. Filters that matter. Reviews from people who've actually been seen.
A community organised around where you are: newly diagnosed, pre-op, recovering, or somewhere in between. Auto-translated, EN ↔ ES.
A structured symptom intake that produces a clinical-register PDF you can hand to your doctor. Not a diagnosis. A door-opener.
Articles by named contributors. Topics covered honestly, including the financial weight of chronic illness.
One-to-one sessions with the founder — lived experience and clinical training, in English or Spanish. USD or MXN.
A persistent button at the top of every page. A fast-loading place to land, with Ale's voice, a tactical guide, and a vetted directory of people you can reach by WhatsApp tonight. Architected for the worst connection on the worst day.
The constraints aren't decoration — they're the product.
A short note when we launch, and nothing else. No marketing. No newsletter you didn't ask for.