Meet Ella, your Lyme+ health companion

Built by patients. Powered by the intelligence of the Lyme+ community.

The hardest part of Lyme+ isn't
just the diagnosis, it's figuring
out what comes next.

You never know if the
next step is the right one.

74% of patients are misdiagnosed first. Every provider, test, treatment, and supplement is a bet of time, money, and hope. A symptom flares and you can't tell: the illness, a Herx reaction, or something new. As one patient put it, it was all a fog.

And figuring it out
falls entirely on you.

Advocate, coordinator, researcher of your own care, exactly when you're least equipped for it: sick, exhausted, and spending upwards of $10,000 to $50,000 out of pocket a year funding your own trial and error treatment. A full-time job you never applied for.

~31m

bitten yearly

(ScienceDirect)

~500k

new cases

up to 20% chronic (HHS)

Fastest-growing

vector-borne illness in the U.S. (HHS)

See what's working.
Know what's next.

Step 1

Step 2

Step 3

Track

Add your story in minutes. Snap pill bottles. Upload labs. Sync your biometrics. Centralized all in one place.

Learn

See what's actually working. What's helping, what's triggering flares, and whether today's crash is a Herx or something new to learn about.

Act

Know your next move. Which provider, test, treatment or habit comes next, decided with your full story in view, so your next step is the best one for you and your time and money go where they help.

I would never hassle my practitioner that much. I can ask Ella anything.

It helps you become an advocate in your own journey. There is real power when you start to see your own patterns.

AI, but built for Lyme+

Around half of chronic Lyme patients carry at least one additional co‑infection or condition — we call this Lyme+. Our tools are trained on leading Lyme+ resources, research, and clinical thinking.

No single doctor or textbook holds all the answers.

The patients living it do.

Every symptom you track and every response you log joins the first real-world dataset built by Lyme+ patients. It becomes:

Ella is already helping Lyme+ Warriors, but don’t just take our word for it.

It is the tool I wish I had access to years ago. It has kept me on track in the most efficient way possible.

Both founders have first-hand experience with Lyme+. You don’t really get it till you get it, and they get it.

It certainly helped my mental health to know that things were going in the right direction.

LymeLess provides me with one central place to monitor and track my Lyme disease treatment and symptoms and gives me insights I wouldn't have otherwise.

It will help you become an advocate in your own journey. There is a lot of power when you start to understand and see patterns.

When I found LymeLess it's like the developer lived in my head.