Our story starts with
Leslie

One person. One long illness. And a conviction about building for the people the system overlooks.

What happened

Leslie's fight began in 2018.

Grad school

While earning her graduate degree at Rutgers, Leslie unknowingly contracted Lyme disease during required fieldwork. One tick bite changed everything.

Five years

She moved back to Texas to start work as a petrophysicist. There, the Lyme went unconsidered for five years. It barely registers in the state, and no one thought to look for it.

The turn

Once the Lyme was finally diagnosed and treated, her immune system (switched on at last) turned on her instead. Lupus.

18 months

Doctor after doctor. Test after test. A year in, the working theory was ankylosing spondylitis, until imaging ruled it out. Lupus is far more common in women of color, so it’s rarely the first guess for a white woman. The average diagnosis takes six years on its own.

Leslie before a second procedure, smiling in a hospital gown
Leslie in hospital during a procedure, covered in an air warming blanket and wearing sunglasses
Leslie before a procedure, smiling in a hospital gown and blue surgical cap
Leslie receiving infusion treatment, wrapped in a blanket, eyes closed
Leslie at a follow-up appointment, smiling in a plaid jacket

Clinic visits, infusions, and surgeries. 2024–2026.

Fall 2024

Dr. Adnan Peer, in Houston, finally named it: Systemic Lupus Erythematosus (SLE). She started Saphnelo®, a monthly infusion. Over the next nine months, piece by piece, she found her way back.

Summer 2025

The medication that felt like a miracle had given her back her strength.

Fall 2025

She earned her promotion, the role she had been working toward since GeoFORCE first set her on the path to geology in high school. The career she set out for, finally hers.

Winter 2025

Then the fight for it caught up with her. The stress of pushing so hard likely tipped her over the edge, and a brutal flare followed.

Spring 2026

The flare bore down on her spine — a series of surgeries over the months that followed.

Now

Out of the flare that began in winter 2025. She is still fighting, still building, and so is Purple Mainspring.

Surya and Leslie in a field of Texas bluebonnets
Surya and Leslie with an eVTOL aircraft in Austin
Surya and Leslie holding their autumn-themed canvases at a paint-and-sip class
Surya and Leslie at the Grand Canyon
Surya and Leslie kayaking side by side down a cypress-lined Texas river
Surya and Leslie ziplining in Costa Rica, holding a Pura Vida sign above a rainforest lake

All the living in between.

Lupus by the numbers

Leslie’s story is unique. Her diagnosis is not.

1.5M
Americans with lupus
90%
Are women
6 yrs
Average time to diagnosis
3
Doctors before the answer
55%
Leave the workforce
$50K
Annual financial burden

Source: Lupus Foundation of America — Lupus Facts and Statistics

Our Why

For three and a half years, Surya was her full-time caregiver — through everything else life piled on in the same stretch.

The caregiving never stopped. The work didn’t either. Held under constant tension, still running.

Which is why at

Purple

the lupus awareness color.

Mainspring

the coiled spring at the heart of a watch, held under constant tension to power everything else.

We build the same way.

Our Pledge

5% of Purple Mainspring’s net profits to the Lupus Research Alliance, every year.
Read the charter

For Leslie. And for everyone still fighting: for a diagnosis, for a treatment, for a way back.