Pre-launch · Waitlist

Your appointment is
10 minutes.
Your pain isn't.

EndoByArtemis helps you turn months of endometriosis and chronic pelvic pain symptoms into one clear picture, built for the appointment where it finally needs to be heard.

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Cyclical pain Bowel symptoms Bladder symptoms Pain with intercourse Infertility Fatigue

Built from 3 months of the patient's own logged entries: not a diagnosis, not a score. A picture of what was actually reported, and when.

Prototype

What logging could feel like

Logged today

A working idea, not the finished app.

9y 4m

The problem

The average time between first symptoms and an endometriosis diagnosis in the UK today, and it's getting longer, not shorter — a delay echoed in health systems worldwide, not a uniquely UK problem. Most of that time isn't spent being investigated. It's spent waiting: for the next appointment, for a referral, for a pattern to finally be taken seriously in a ten-minute slot.

Endometriosis UK, State of Endometriosis Care, 2026

What EndoByArtemis does

Three things, done properly: nothing gimmicky bolted on top.

01

Track what actually happens

Pain, bleeding, and bowel or bladder symptoms, including pain opening your bowels or pain during sex, fatigue, diet and lifestyle notes, and more, logged on any day, not just around a period. Chronic pelvic pain doesn't wait for your cycle, so this doesn't either.

02

Arrive with a clear picture

Months of entries, organised into one visual summary across the endometriosis and chronic pelvic pain patterns clinicians already look for, built to be read in the time you'll actually get.

03

Understand what you're facing

Plain-language, clinically written content on endometriosis and chronic pelvic pain: what's known, what a laparoscopy can and can't tell you, and what to realistically expect.

What EndoByArtemis isn't

Not a diagnosisEndoByArtemis organises what you tell it. It never tells you what it means. That stays with your doctor, always.

Not a replacementIt doesn't stand in for your doctor or gynaecologist, and it doesn't replace the communities where people already understand what you're going through. It's something you bring with you.

Not a promiseAt best, it might help things move faster. At the very least, you'll walk in with a clearer account than memory alone gives you.

Why I'm building this

Ten minutes rarely captures the real shape of months of symptoms: how often, how severe, how it's actually changed. That's not down to any one clinician. It's a structural problem, and it's one a better-prepared conversation can help with.

Chronic pelvic pain isn't automatically endometriosis, and having endometriosis doesn't automatically mean severe symptoms. How much disease is found at surgery and how much pain someone is in don't reliably line up. Patients deserve to know both.

We still don't fully understand why endometriosis happens. The textbook explanation is only part of a far more complicated picture researchers are still working out, and pretending otherwise doesn't help anyone.

After years of not being believed, wanting a diagnosis, any diagnosis, just to feel validated is completely understandable. But a label was never really the goal. Feeling better is. That's what this is built toward.

Surgery has a real place in treatment, but it isn't a guaranteed fix, and it isn't the only option. The more conservative path is sometimes the better one, and every patient deserves that conversation, with realistic expectations, not a historical default.

Our job isn't to promise a cure. It's to help you arrive at that conversation with a clearer picture, and to be honest about what's actually known, not what's easiest to say.

EndoByArtemis is a symptom-tracking and education tool, not a diagnostic device, built that way on purpose.

If that sounds like what you've been looking for, join the waitlist →

What's next

Two ideas we're exploring, not promises.

Tracking and appointment prep don't cover everything people are looking for. These are two gaps we know about and are actively thinking through, not features that exist yet.

Exploring

A space to hear from people who get it

No amount of tracking replaces hearing from someone who's actually lived it. A community layer, built with the same restraint as everything else here, is something we're exploring, not something we've built.

Exploring

Help finding the right specialist

A gynaecologist, a pelvic health physiotherapist, a therapist, a nutritionist. Who's actually worth seeing is usually passed around by word of mouth. We're exploring ways to make that easier and more reliable to find.