April is HIE Awareness Month! Download our comprehensive toolkit, calendar of events, and opportunities to dig into advocacy, awareness, education and support to improve the quality of life for children and families impacted by neonatal and pediatric-acquired Hypoxic Ischemic Encephalopathy. Learn More
This is a video support group starting for loss families. Parents and legal guardians who have lost their children due to HIE, either at birth or in childhood, are invited to participate in our monthly support group. Led by Hope for HIE’s social worker, Vanessa, families will be engaged in a space of support, connecting with others to build connections. These events […]