Hope for HIE – Hypoxic Ischemic Encephalopathy Hope for HIE – Hypoxic Ischemic Encephalopathy

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Hope for HIE partners with Neuren to support development of NNZ-2591

Hope for HIE partners with Neuren to support development of NNZ-2591

September 9th, 2025  | Advocacy  | News  | Research

Melbourne, Australia: Neuren Pharmaceuticals (ASX: NEU) has commenced a formal partnership with Hope for HIE supporting development of NNZ-2591 to treat hypoxic-ischemic encephalopathy (HIE). Hope for HIE is the global organization connecting families, researchers, clinicians, biotech and more to improve the quality of life for children and families impacted by neonatal and pediatric-acquired Hypoxic Ischemic Encephalopathy, a type of brain […]

Coping Plans: Helping Kids Feel Confident, Calm, and Supported

Coping Plans: Helping Kids Feel Confident, Calm, and Supported

September 5th, 2025

Big or small, new experiences can feel overwhelming for kids—especially when it comes to medical tests or hospital visits. One way to help is by creating a coping plan. What is a Coping Plan? Think of it as a personalized guide that highlights what helps your child feel calmer, safer, and more in control when things feel stressful or tough. […]

September is NICU Awareness Month

September is NICU Awareness Month

August 29th, 2025

The NICU is a place no parent expects to be, yet for many families in our community, it’s where their journey with HIE begins. Those early days can bring uncertainty, questions, and unexpected challenges, and the experience can feel overwhelming at times. NICU Awareness Month is an opportunity to recognize these experiences, honor the resilience of families, and highlight what […]

Navigating Back-to-School Transitions: Child Life Key Takeaways

Navigating Back-to-School Transitions: Child Life Key Takeaways

August 28th, 2025  | Advocacy  | Child Life Resources  | News  | Resources

As many families in our community know, the transition back to school encompasses more than gathering supplies and setting schedules—it’s about easing the change with comfort, predictability, and connection. Most importantly, it’s about helping your child feel secure and supported, no matter what comes their way. That’s why Annie Gunning, CCLS, is sharing flexible strategies and practical tools you can […]

A Milestone for HIE Research: First Family Enrolled in the HIE Community Research Registry

A Milestone for HIE Research: First Family Enrolled in the HIE Community Research Registry

August 19th, 2025  | Advocacy  | HIE Registry Updates  | News  | Research

We are thrilled to share an exciting milestone for our community: the HIE Community Research Registry has officially enrolled its very first family at Colorado Children’s Hospital. This marks the beginning of a groundbreaking effort to better understand the long-term impacts of Hypoxic-Ischemic Encephalopathy (HIE), improve care, and drive innovation in research. For too long, families impacted by HIE have […]

SHARE YOUR HIE STORY

One of the ways many HIE families work through the trauma of their journey is sharing their story to help other families who will find us in their own HIE journey. We hope you’ll take a few minutes and share yours with us. We’ll publish it to our Family Stories blog!

Share Your Story

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