Impact

Built on a Proven Commitment to Children with DIPG

Before founding the Brave Ronil Foundation, Manisha and Milan Mehta spent years helping fund pediatric brain cancer research, support affected families, and raise awareness. That experience is the foundation we carry forward.

FOUNDERS' IMPACT

What Our Founders Helped Achieve Through Their Prior Work

The impact below reflects work our co-founders, Manisha and Milan Mehta, helped achieve over years of pediatric cancer advocacy and fundraising before founding the Brave Ronil Foundation. BRF is a new, independent organization and does not claim these accomplishments as its own.

50 +

Families supported

$ 462900

Research funded

Across 9 projects at leading medical institutions

9

Research Projects

 At institutions including UCSF, Stanford, Dana-Farber, and U of Michigan

Years
8

Fighting DIPG

Since Ronil’s passing in 2018

What We're Building

What the Brave Ronil Foundation Is Working Toward

The Brave Ronil Foundation is a new, independent 501(c)(3) organization working to create a lasting impact in three areas.

  • Fund Research
  • Support Families
  • Raise Awareness

Fund Research

We are working to fund research grants and clinical trials that bring us closer to a cure for DIPG.

Support Families

We are building resources, financial support, and guidance so no family faces DIPG alone.

Raise Awareness

We are raising awareness in our communities so this disease is no longer overlooked.

Programs & Initiatives

Building on Years of Research, Awareness, and Community Advocacy

Research Grants

A Future Driven by Research and Hope

BRF will fund clinical trials, early-stage research, and partnerships that advance treatment for children with DIPG.

  • Clinical Trials
  • Preclinical Research
  • Research Partnerships
A Future Driven by Research and Hope

CureFest

Building a Stronger DIPG Community Through CureFest

CureFest for Childhood Cancer is an annual gathering in Washington, DC during Childhood Cancer Awareness Month that brings together families, foundations, researchers, and lawmakers as one voice against childhood cancer. We participate in CureFest to represent DIPG families, raise awareness, and join hundreds of childhood cancer organizations advocating for increased research funding and better treatments.

Building a Stronger DIPG Community Through CureFest

BrainStorm Summit

Connecting Minds for Pediatric Brain Cancer Research

Our co-founders and advisory board have participated in the BrainStorm Summit, engaging with researchers, families, clinicians, and advocates to share insights, explore emerging treatments, and support future collaboration in pediatric brain cancer research.

Connecting Minds for Pediatric Brain Cancer Research

FOUNDERS' ADVOCACY

Turning Loss Into Law: AB 703

In 2025, Ronil's younger brother, Sahil Mehta, helped pass California Assembly Bill 703, the state's first voluntary tax check-off dedicated to childhood cancer research. Signed by Governor Newsom in July 2025, AB 703 lets Californians donate a portion of their state tax refund to pediatric cancer research beginning in 2026.

Sahil brought the idea to Assemblymember Alex Lee, testified before the legislature, and rallied support. The bill was co-sponsored by the American Cancer Society Cancer Action Network and the Brave Ronil Foundation.

This work predates the Brave Ronil Foundation and reflects our founding family's advocacy. Sahil continues to advocate nationally for pediatric cancer research, continuing Ronil's legacy and helping other families to bring the AB 703 model to other states.

Together, We Can Bring Hope to Children Facing DIPG

Your support helps fund research, support families, and raise awareness for children battling DIPG

Join Us in Helping