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Tuesday, September 30, 2025

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NewsDesk Milli Chronicle September 30, 2025September 30, 2025 affordable rare disease medicines, AIIMS rare diseases, Ayushman Bharat rare disease coverage, caregiver support India, government support rare diseases, healthcare access India, healthcare challenges rare diseases, Hunter Syndrome India, India rare disease awareness, India rare disease initiatives, India rare disease policy, medical advocacy India, MPS II awareness, National Hunter Alliance, NRDP implementation, patient care India, pediatric rare disease treatment, rare disease advocacy India, rare disease healthcare solutions, rare disease patient support, rare disease policy reform, rare disease research India, rare disease summit 2025, rare disease treatment gaps, rare disease treatment India, Rare Diseases India Foundation

India Unites for Rare Disease Patients at Hunter Alliance Summit 2025

New Delhi – The National Hunter Alliance Summit 2025, held on September 27 in New Delhi, brought together patients, caregivers,