Yuvaan Tiwari Foundation

03/25/2026

03/12/2026

Yuvi would have turned 8 today. It’s hard to make sense of how time can stand still yet carry forward.

We miss you every day, more than words can express. Your laugh, your warmth, your boundless energy, your love for life. Your presence is still felt so strongly and the love you left behind continues to comfort us, inspire us and guide us forward.

We feel blessed and deeply grateful for the precious time we shared with you. A time that is now sacred to us.

Happy birthday to our love, our light, our brightest star! 🎂

12/31/2025

Our foundation was created four years ago with a promise to do something meaningful with the love we carry for Yuvi, and to turn our loss into hope for other children and families facing brain cancer.

We are grateful to share that this year we funded $1,075,500 to accelerate pediatric brain cancer treatments through research grants and mission-aligned investments. Additionally, we provided financial support to help 24 families battling DIPG/DMG with rent, medical and travel expenses.

This progress represents our belief in transformative science, trust in collaboration, and a shared commitment to pushing for better outcomes.

None of this would be possible without our supporters, the scientists who dedicate their careers to this field, and the partners and foundations who stand alongside us.

As we move into 2026, our resolve is stronger than ever to back bold science, move faster than the status quo, and help change the trajectory of pediatric brain cancer.

Happy New Year!

10/01/2025

When a child is diagnosed with DMG/DIPG, every day becomes an act of courage. Courage to endure the hospital stays, the scans, the harsh side effects, the endless pokes and prods. Courage to keep smiling and loving, even when their bodies are failing them.
That kind of courage doesn’t end when September does. Childhood Cancer Awareness Month may be closing, but their fight continues every single day. And so must we.
This disease doesn’t discriminate. Any child. Any family. Any day. That’s why our mission can’t be confined to a single month on the calendar. It must carry on until no child is lost to brain cancer and no family hears the words, “there’s nothing else we can do.”
Let's honor the strength of these children by raising our voices — louder, longer, and beyond September. 🎗️

09/29/2025

At just six years old, Lexys shined with a heart as big as her smile. Diagnosed with DIPG in 2014, she faced 13 months of treatments and trials with extraordinary courage — never once complaining, even as her body grew weaker.
Lexys adored princesses. She was known for her kindness, always checking on other children in the hospital and sharing her light wherever she went. “Ten seconds of knowing her, you fell in love with her,” her family says.
Today, we remember Lexys not just for her battle, but for her love, laughter, and bravery. 💛

09/28/2025

Jase lives life to the fullest, fueled by his love for sports, adventure, and the unwavering support of his family and community. Whether he’s cheering on his favorite teams—the Minnesota Timberwolves and Vikings—playing baseball and basketball, or racing Hot Wheels and monster trucks at home, Jase embraces every moment with enthusiasm.
Jase’s childhood took an unexpected turn in November 2024 when he was diagnosed with DIPG. Like a true sports fan, Jase is willing to do what it takes to win and is currently part of a clinical trial at Children’s Minneapolis. 💛

09/26/2025

Maddie is happiest when she’s surrounded by her family and friends. She adores horses and dreams of having one of her own someday. Her light shines brightly—she has an infectious laugh and a kindness that touches everyone she meets.
On October 1, 2024, Maddie was diagnosed with DIPG, the most aggressive form of childhood brain cancer. Yet through countless hospital visits, pokes, and procedures, even as her world has been turned upside down, Maddie has faced it all without complaint. Her strength and spirit inspire all who know her. 💛
https://www.caringbridge.org/site/c344adcb-8450-11ef-b01a-37f62a5b2c6b

09/24/2025

6-year-old Carter fought DMG with the courage of a true warrior. But what stood out the most was his never-ending sense of humor. Even in the darkest, toughest moments, Carter could easily put a smile on everyone’s faces. He especially loved a well-timed fart or p**p joke! At school he became known for his wacky dance moves, his giant giving heart, and his brighter-than-the-sun smile. Obsessed with Iron Man, Carter became a real life super hero through his battle with DMG. Carter is missed deeply, and his absence is felt in every moment. 💛

09/23/2025

8-year-old Isla was full of energy before being diagnosed with . Always very happy and playful. Friendly and outgoing. She loved her Heelys and wore them everywhere. She also loved gymnastics, family getaways, eating at restaurants, dancing and singing with her sisters, Briella and Elisse. Isla passed way on April 24 after a brave fight. 💛

09/21/2025

Jaisyn was musically inclined and athletic, playing football, baseball, and the trombone. He loved singing and would always sing himself to sleep or while in the shower. He was an avid gamer who played Fortnite a lot. Jaisyn also loved playing in the backyard with his dog Sampson. On January 16, 2020 Jaisyn was diagnosed with at 13 years old. He did a clinical trial at St Jude's in Memphis. Jaisyn sadly gained his wings on December 12, 2020. He would have graduated from high school this year but remains forever 14. 💛

09/19/2025

Enguerrand was born on June 15th, 2004 in France. He was a kind, smart, and athletic young boy with lots of energy. Enguerrand enjoyed traveling, going to school, and being outside. His favorite sport was tennis, and he aspired to be a pro tennis player. He won several tournaments and was ranked in the sport. Enguerrand had lots of personality and made friends easily.
On June 15, 2017 Enguerrand celebrated his 13th birthday. The 5th grade year had gone well and he was participating in many sports competitions. But around that time an unusual fatigue set in, followed by vomiting, loss of strength in his left hand and balance problems. Enguerrand had a brain scan in July 2017 and was diagnosed with - a death sentence: an incurable and inoperable cancer.
Throughout his battle, Enguerrand had a wide support network - family, friends, top athletes. He fought long and hard like a true warrior, accepting all the treatments, enduring everything that is humanly possible to endure, but always with a smile until the very end. Enguerrand passed away on July 9, 2018. He is loved and missed beyond measure. 💛

For Childhood Cancer Awareness Month, please consider supporting research through the Association Warrior Enguerrand: https://www.helloasso.com/associations/warrior-enguerrand/formulaires/1

09/18/2025

Johana was diagnosed with DIPG on May 24, 2024. In April she underwent a second course of radiotherapy and was in a clinical trial in Paris. She is taking ONC201. Named after Joan of Arc, Johana carries the same spirit of bravery and determination. 💛