MEMF co-founders Corrina Clover Miller and Marta Eliza Miller standing back to back
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Marta Eliza Miller Foundation

SCOLIOSIS AWARENESS · YOUTH SUPPORT · RESEARCH & CARE

Helping young people and families face scoliosis with education, stronger care and a community built around hope.

Marta Miller strikes a figure-skating pose in front of the Children’s Hospital Los Angeles blocks MARTA’S STORY Read their story A diagnosis became a movement. Marta and her mother Corrina turned uncertainty about her future on the ice into a foundation helping young people with scoliosis feel less alone.

What your support makes possible.

From grants that reach every state to tools that can make care less disruptive, these are the programs behind the headline numbers.

$250K NATIONAL INITIATIVE

Care, coast to coast

The $250,000 national initiative supports pediatric hospitals, healthcare providers, advocacy organizations and community partners in every state and Puerto Rico.

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$475K+ TO CHLA

A lasting home at CHLA

MEMF support for the Gene and Jackie Autry Spine Center now exceeds $475,000, and two rooms at the hospital carry the foundation’s name.

See the partnership
MOMENTUM SPINE

Smarter monitoring at home

MEMF helped launch CHLA’s Momentum Spine pilot, which uses a short smartphone video and 3D scanning to help clinicians track spinal curves between visits.

See the pilot
YOUTH & FAMILIES

Knowledge, stories and community

Awareness resources and lived-experience conversations help young people and families understand scoliosis and feel less alone in the process.

Explore awareness

Meet the mission.

Hear how Marta’s experience as a young athlete grew into a foundation built to help other young people stand taller through scoliosis.

The work keeps moving.

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