NEWS ABOUT THE CURE
Temporary Pause on Federal Grant Funding: The Urgent Need for Your Support is Clear
January 30, 2025
In the face of growing uncertainty, we find ourselves in a critical moment where your help is needed more than ever. Groundbreaking cancer research —the kind that holds the potential to save lives—is at risk of being underfunded this year by federal sources, and the children who need it most are already waiting for hope. This is why private funding of research, like that done by The Cure Starts Now, is vital. Built by a community of families, we have witnessed children fight brain cancer with…
Bringing Us Closer to a Cure
January 6, 2025
Thanks to your incredible support, The Cure Starts Now and the DIPG/DMG Collaborative have funded 17 grants during the 2024 grant cycle! That's 17 opportunities to make groundbreaking strides toward curing cancer. When we fund research, we’re not just fulfilling the dreams of our families and warriors who wish for a cure—we’re also supporting the researchers who dedicate their lives to turning those dreams into reality. We often tell our researchers that we have the easy job of raising the…
Family Never Fights Alone
August 21, 2024
When Cara’s three-year-old son, Cameron, was diagnosed with ependymoma, her world was turned upside down. Like any mother, she was determined to do everything in her power to help her child. Cara immersed herself in research, connecting with others in online brain cancer support groups to learn as much as possible about her son’s condition. It was in one of these support groups that Cara met Lauren, a mother facing a similar battle. Lauren’s five-year-old daughter, Cana, had just experienced a…
Little Girls, Big Miracles
July 2, 2024
Clare (8) and Mackenzie (9) are DIPG Warriors defying the odds as they reached 6-years post-diagnosis! Clare, Ohio, age 8 Marking the 6th anniversary of diagnosis day was bittersweet for the Ronnebaum family. "We are so very lucky," wrote Clare's Mom. 6 years ago, her parents were told Clare would only have 8-11 months to live. As they celebrate her continued stable scans, they are also reminded of all the children facing DIPG who don't get to celebrate this milestone. At the time of her…
Wyatt's Victory Garden: Cultivating Hope in the Face of Childhood Cancer
March 26, 2024
In the heart of a small town, nestled amidst fields and farms, there resides a special little boy named Wyatt Reber. At just three years old, Wyatt was diagnosed with ependymoma, a rare form of brain cancer. As the cherished first child of Alexa and Matt Reber, he possesses a gentle soul that radiates kindness. Though initially shy around new faces, his warmth and innocence captivate all who have the privilege of meeting him. With a protective nature towards his little sister, Wyatt embodies…
Hope Rising: Funding Progress in DIPG Research
March 26, 2024
In their tireless pursuit of effective treatments for pediatric brain cancers, Dr. Biplap Dasgupta and his team at Cincinnati Children’s Hospital Medical Center stumbled upon an unexpected existing compound that exhibited promising results in targeting specific mutations within DIPG models. The potential of this compound to halt tumor growth would make a significant stride forward in the battle against this aggressive form of brain cancer. What sets this discovery apart is its potential to…
Promising Pathway Act (PPA) Family Stories
October 24, 2023
The Promising Pathway Act (PPA), introduced by Senators Mike Braun, Kirsten Gillibrand, Lisa Murkowski, Kevin Cramer and Roger Wicker in June of 2023 is a revolutionary bill changing how current FDA guidelines are applied with terminal and rare diseases like DIPG, DMG and Medulloblastoma. It’s key provisions not only provide a method to allow promising therapies to move faster for the patient with a conditional approval process, but also affirms that any provisional approval is backed with a…
Graeter's Ice Cream Sets Record Year, Raising $290,000 to Help Find the Homerun Cure™ for Pediatric Brain Cancer
October 3, 2023
Graeter’s and The Cure Starts Now continue to pave the way for sufficient cancer research funding Cincinnati, OH (September 28, 2023) — Cincinnati-based Graeter’s Ice Cream completed its annual Cones for the Cure campaign – an 11-day event that offers guests a unique way to support The Cure Starts Now and pediatric brain cancer research. This record-breaking year, Graeter’s will donate $290,000 as a result of guest support, company donations and ice cream sales of the seasonal favorite, Elena’s…
Connor’s “CURE”sade Against Cancer
September 28, 2023
Connor George is a spunky little boy who sees magic in every part of his life. He looks at the world with absolute joy and an open heart. Much of Connor’s young life was spent in the hospital when he was diagnosed with medulloblastoma . After his diagnosis, his mother Brooke began researching for information, education, and organizations that specialized in pediatric brain cancer leading her to discover The Cure Starts Now. After months of research, Brooke determined The Cure Starts Now’s…
17th Annual Cones For The Cure Campaign Launches with a Larger Than Ever Fundraising Goal
September 1, 2023
The Cure Starts Now and Graeter’s Ice Cream Partnership strives to find a “Homerun Cure™” for Childhood Cancer CINCINNATI, OH (September 1, 2023) – Graeter’s Ice Cream , a 153-year-old, family owned craft ice cream company, has again partnered with The Cure Starts Now in its 17th annual campaign in support of finding the Homerun Cure™ for childhood cancer. The campaign gives ice cream lovers a unique way to support this increasingly important cause and brings hope to those in need while…
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