Today, we join together to wear GREEN and highlight our children and families who are also a part of the cerebral palsy community -- roughly 40% of all HIE cases will get a subsequent diagnosis of Cerebral Palsy. Learn More  

We're excited to have Amy on our Board of Directors, and serving as the co-chair of our Medical Advisory Board! Be sure to join us to learn about Amy's journey, both as a HIE parent and a pediatric occupational therapist... how those worlds have come together, and how she's working with the foundation to connect with researchers and clinicians, all […]

Ravi and Sarah Shah invite you to celebrate as their son, Kiran gets ready to turn ONE by raising a glass to him and raising support for Hope for HIE.   "We wanted to give back to the foundation that gave us so much hope, support, and piece of mind. Kiran was diagnosed with HIE (hypoxic ischemic encephalopathy), a type […]

Join us as we kick-off our #GivingTuesday efforts over on Facebook. Giving Tuesday Event Information

HIE is the second leading cause of Infantile Spasms, a rare type of epilepsy that requires quick diagnosis and frontline treatments. The onset of Infantile Spasms is considered a medical emergency. We have developed comprehensive resources, in conjunction with the Infantile Spasms Action Network, to better educate our families, especially those in the first year of their HIE journey. Learn […]