Yuvaan Tiwari Foundation

Yuvaan Tiwari Foundation We fund research to find a cure for fatal pediatric brain cancers and support impacted families.

Our mission is to find a cure for diffuse midline gliomas (DMGs) and other fatal pediatric brain cancers, while supporting patients and families along their journey. ADVANCE RESEARCH
We fund scientists, physicians and institutions to accelerate promising research that will improve diagnosis, treatment effectiveness and outcomes. EMPOWER FAMILIES
We make a difference in the lives of afflicted families by offering resources and financial assistance to enable a better quality of life. INSPIRE ACTION
We raise awareness of the devastating impact of pediatric brain cancer and rally support to find and fund a cure. Every day, thirteen children are diagnosed with a brain tumor, the deadliest and most common form of pediatric cancer yet less than 4% of federal funding is directed at pediatric cancer research, with only a small fraction of these funds being used for brain tumor research. Foundations like ours are critical to funding research to find a cure. The Yuvaan Tiwari Foundation was established in 2021 by Parvati and Satya Tiwari to honor the legacy of their son Yuvaan (Yuvi). At age two, Yuvi was diagnosed with a rare and deadly brain tumor called diffuse midline glioma (DMG). Yuvi bravely fought DMG for seven months, enduring thirty days of radiation therapy, multiple surgeries, countless doctor visits and MRIs, and several hospital stays. The Yuvaan Tiwari Foundation is built on love, hope and an unwavering determination to find a cure for DMG. Focused research on rare brain tumors like DMG has the potential to uncover new avenues of treatment not just for children with brain tumors, but also for other childhood and adult cancers.

Yesterday, Karter should have celebrated his 10th birthday. For his parents and loved ones, a day that should be filled ...
09/27/2026

Yesterday, Karter should have celebrated his 10th birthday. For his parents and loved ones, a day that should be filled with celebration carries the profound absence of a sweet boy who brought so much joy to their lives.

Karter was an active, smart, and loving boy who enjoyed sports, school, and family outings. He was a devoted Edmonton Oilers fan who loved his family, friends, and pets. From toddlerhood through his final days, swimming was one of his favorite activities.

Whether playing basketball with his cousin, hockey in the living room, or baseball with his team, Karter brought energy to everything he did. He was sweet and caring, always with a smile, a song to sing, dance moves like no other, and a heart of gold.

DIPG stole Karter’s life, but not the love, courage, and light he shared. He used his experience to teach so many people so much. Today, and always, we honor Karter as a hero ✨



Karters Cancer Crusade

Owen was a beautiful little boy inside and out. He was so incredibly loving and always thought of others before himself....
09/24/2026

Owen was a beautiful little boy inside and out. He was so incredibly loving and always thought of others before himself. He wanted to be a robot fireman when he grew up. Owen fought DIPG with so much courage, strength and grace. He was such a tiny boy but he was so brave and is forever his family’s hero…and ours. 🦸‍♂️

Talin was a bright and curious boy, mischievous and full of love for his older brother Tristan and younger brother Kian....
09/22/2026

Talin was a bright and curious boy, mischievous and full of love for his older brother Tristan and younger brother Kian. He loved learning, going to school and cuddles. Talin was diagnosed with DIPG on the 11th of April at age 5 and died in his father’s arms just 13 weeks later.
Talin is alive as a cell line at The Children's Cancer Institute of Australia and was one of the very first cell lines in Australia. Two people are seeing out of Talin’s eyes and the difference he has to the DIPG community is amazing. Talin is partly responsible for a new clinical trial in DIPG with other Australian Children's Cell Lines. Talin is missed to the stars and back...plus a little bit more. 💛

6-year-old Carter fought DMG with the courage of a true warrior. Carter was the light and laughter in every room. But wh...
09/19/2026

6-year-old Carter fought DMG with the courage of a true warrior. Carter was the light and laughter in every room. 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 touched so many lives in his community, teaching those around him that you can find so much joy and light even in the darkest moments. ✨

Cassiopeia was a truly unique individual. She was independent, a kind of social maverick who didn’t just march to the be...
09/16/2026

Cassiopeia was a truly unique individual. She was independent, a kind of social maverick who didn’t just march to the beat of her own drum—she inspired others to march right alongside her. She was a patient leader, a kind friend who was effortlessly cool, and had the wit and humor of a veteran stand-up comedian.

She had a mental library of music that seemed well beyond her years. When you needed a song, she knew exactly the right one and made sure to share it with you, even if she had to sing it herself. Her humor and ability to read people also came through in her art. A creative pen-and-marker artist, Cassie captured her environment and the people around her with a whimsical perspective.

Cassie was deeply religious and never hesitated to share her beliefs. Her faith was an important part of who she was and how she lived her life.

Cassie lost her life to DIPG just two days shy of her 14th birthday. She is deeply missed by those who knew and loved her.

Mila was hilarious and witty, thoughtful and selfless, bold and brave. She was kind, generous, headstrong, independent a...
09/15/2026

Mila was hilarious and witty, thoughtful and selfless, bold and brave. She was kind, generous, headstrong, independent and unapologetically herself.

A true girl’s girl and fiercely loyal friend, Mila led with integrity, acceptance and genuine support, making people feel comfortable being themselves. She loved cheerleading, flag football and musical theater, where she proudly earned lead roles. She also loved crafting, music, dancing, shopping, Jellycats, tasteful pranks and her collection of hundreds of NeeDohs.

Above all, Mila loved her family and friends. Throughout her fiercely fought battle with DIPG, she held onto hope and her unwavering faith in God.

Mila passed away at age 13 in July 2026. Her life was far more than the illness she faced. She will be remembered for her humor, creativity, kindness, courage and faith, and for the love she shared with those around her.

www.momentswithmila.com

Creative and talented, Chloe was a sensitive soul and a true artist at heart. She was passionate about art, played cello...
09/12/2026

Creative and talented, Chloe was a sensitive soul and a true artist at heart. She was passionate about art, played cello and piano, and acted in various theatre productions. Chloe loved Japanese anime, and her favorite color was purple.
Chloe excelled academically as a bright honor roll student and was an active member of her elementary school’s student council and newspaper club. She played soccer and enjoyed snowboarding with her dad and shopping and crafting with her mom.
Chloe loved every animal she encountered and dreamed of being a veterinarian. She was as kind, empathetic, brave, determined and thoughtful as a person could be, and left a lasting impact on all who knew her. Sadly, Chloe passed away from DMG at age 13.

Onyx Broly Brown was born January 28, 2021, during Covid, bringing immense joy and hope to his family. From the beginnin...
09/11/2026

Onyx Broly Brown was born January 28, 2021, during Covid, bringing immense joy and hope to his family. From the beginning, Onyx was a strong and determined little boy. He crawled at six months, took his first steps at one year, and showed remarkably advanced speech for his age. When diagnosed with DIPG in 2024, Onyx became a true warrior. Despite losing his mobility, he repeatedly fought his way back through intensive therapy. With incredible courage, Onyx became the first child in BC Canada to undergo a groundbreaking medical trial, giving hope to new possibilities for children facing this disease. He treasured adventures with his brothers and created unforgettable memories with his family. Onyx's journey came full circle as he passed away on September 20, 2025. Onyx’s courage, resilience, and loving spirit continue to inspire everyone who knew him.
https://heartsforonyx.com/

Ellerie was full of life and magic. Everyone she met fell in love with her and she had an amazing ability to make everyo...
09/09/2026

Ellerie was full of life and magic. Everyone she met fell in love with her and she had an amazing ability to make everyone giggle even on the hardest of days. She was a sassy, gorgeous, kind and happy little girl who fought with so much determination and strength. She was at her happiest singing and dancing and spending time drinking cups of tea while watching Christmas films!




Ellerie's Glimmersfinding.glimmers

Yuvi was a warm, happy and loving boy. He liked being the center of attention and the source of endless amusement and la...
09/05/2026

Yuvi was a warm, happy and loving boy. He liked being the center of attention and the source of endless amusement and laughter for everyone around him. He enjoyed learning new things and could name fruits, vegetables, bugs and vehicles from A to Z. His favorite color was yellow, he loved the sunshine and always saw the bright side. None of this changed, even after he was diagnosed at age 2 with the deadliest form of brain cancer – diffuse midline glioma (DMG). Yuvi lived each day of his short life with joy. He is our hero and inspiration, the force that drives us to continue the fight for other children and families.

We never imagined childhood cancer would touch our family —until it did. Now, we know how much every act of support matters to draw attention and funding to accelerate the path to a cure. This please stand with the brave children and families facing the unimaginable: share the post, wear the t-shirt, make the donation, tell someone about the brave child you read about or have/had the honor of knowing.

Address

PO Box 570753
Atlanta, GA
30357

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