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Congress kicked the FY 2027 funding can down the road, extending federal appropriations only through December 11, 2026 — leaving pediatric research advocates on edge. The Child Neurology Society (CNS) is pushing back, urging evidence-based vaccine recommendations for children with complex neurological conditions and meeting with Sen. Duckworth's office to champion NIH funding, rare disease research, and telehealth access.
Congress extended federal funding only through December 11, 2026, punting FY 2027 appropriations to a post-election lame-duck session. For pediatric neurologists and researchers, that uncertainty is more than a budget headache — it puts NIH grant continuity and long-term research planning at risk for some of medicine's most vulnerable patients.
The Child Neurology Society (CNS) isn't sitting on the sidelines. On September 15, CNS submitted formal comments to HHS calling for clear, evidence-based vaccine recommendations and timely immunization protocols — especially for children with complex neurological conditions, who face heightened risks from vaccine-preventable diseases. CNS representatives also met directly with Sen. Tammy Duckworth's office on September 29 to press federal priorities including sustained NIH funding, rare neurological disease support, and continued telehealth access.
Key Takeaways:
Why it matters: With pediatric neurological conditions often underfunded and underrepresented in policy discussions, CNS's proactive engagement on Capitol Hill signals the stakes — and the urgency — of keeping these issues front and center as federal budget battles unfold.