Dealing with lupus is a full-time job.

Get proactive insights for your lupus trends across wearables, your medical records, sleep, skin temperature, heart rate, lab results, joint pain, fatigue, sun exposure, medications, and flares.

For free. Today.

Scientists, doctors, and patients collaborating on autoimmune research

Join the waitlist.

How it works

Three steps. That's it.

  1. 1 · Connect

    Everything about your health, finally in one place.

    Gather connects your medical records, labs, wearables once — then it stays in sync on its own.

  2. 2 · Just text

    There's nothing new to navigate. It's a conversation.

    Gather checks in with short questions tailored to your lupus, and you just answer — by text or voice note.

  3. 3 · Know your trends

    We track your trends and send insights made only for you.

    Gather learns how your lupus behaves and helps you navigate the days ahead.

    Optional: free blood testing during flares — a nurse comes to your home, so your picture goes deeper than symptoms and medical records alone.

We empower you on your toughest days.

Your toughest days hold the biggest clues. Free at-home blood draw within 48 hours of a flare, measuring thousands of markers instead of dozens, so you and your care team can see what's driving your flare.

Built with input from patients.

I have a million apps on my phone. The app goes defunct, or it just doesn't do enough.

Lupus patient · 20+ years since diagnosis

She was like, "Are you hurting today?" I was like, no — but I was hurting last week.

Lupus patient · diagnosed after 21 years of symptoms

I found one that had the symptoms, but I couldn't track sleep or what I was eating. So I was doing it in two places.

Lupus patient · diagnosed in high school

"When you're having a flare, get your blood work done." I couldn't make it out of the bed. It never got done.

Lupus patient · symptoms since age 10

I still don't know what's happening in my blood.

Lupus patient · never in remission

Blood work is every three months. But I don't hurt then.

Lupus patient · on routine monitoring

I kept a little black book of what I was experiencing and what I was eating. An app would have been way easier to cross-reference.

Lupus patient · diagnosed at 19

We literally called it a mystery illness for over a decade.

Lupus patient · symptoms since age 10

Love to just be normal for a minute. That'd be great.

Lupus patient · diagnosed in high school

Your frustration belongs here too.

Tell us what's broken — it shapes what we build next

One of our first 100 members.

Work directly with our team and shape Gather around your lupus: your symptoms, your routines, your toughest days.