Key Takeaways: Cure 4 The Kids Foundation is Nevada’s only dedicated pediatric cancer and rare disease treatment center, treating nearly 10,000 patients each year at
Key Takeaways: The Nevada State Board of Medical Examiners (NSBoME) is seeking a public, non-medical representative to serve on its Genetic Counseling Advisory Council With
Key Takeaways: The United Nations is poised to formally recognize childhood cancer in its Fourth High-Level Meeting on Non-Communicable Diseases—a historic first that could reshape
Key Takeaways: What are the AKAC and GKAC Acts? Two bipartisan federal bills working to remove systemic barriers in pediatric cancer and rare disease care
Key Takeaways: Nevada receives among the lowest NIH funding in the nation—ahead of only Alaska and Wyoming—making our research ecosystem especially vulnerable to federal cuts.
Key Takeaways: Nevada’s Rare Disease Advisory Council (NV-RDAC) has launched comprehensive Patient & Family and Healthcare Provider Needs Assessments to gather critical insights about rare
Key Takeaways: On September 30, 2025, the U.S. Department of Health and Human Services announced a decision that will reshape the future of pediatric cancer
Key Takeaways: A new Executive Order directs federal funding and resources specifically toward using AI technology to improve pediatric cancer diagnosis, treatment, and outcomes. The
LAS VEGAS – October 1, 2025 – Today, Cure 4 The Kids Foundation (C4K) debuted its newest themed patient exam room – an effort to