We know summer camp can be a magical experience—full of connection, growth, and plain old fun. But for many of our families, the decision to send a child to camp often comes with a few extra layers to think through. Medical needs. Accessibility. Safety. Inclusion. It can feel like a lot. That’s why we invited Angela Bryan, Certified Child Life […]
Access to mental health support and resources is critically important for families who find themselves in the NICU and PICU. Parents whose children are admitted to the NICU or PICU have a 45-50% greater incidence of mental health disorders such as PTSD, Anxiety & Depression. There also remains significant inequity for non-white, non-preemie, non-maternal patients and families in the NICU, […]
Medical procedures can be overwhelming, especially for kids. But what if there was a simple way to make those moments feel less scary and much more manageable? That’s where comfort positions come in—they’re a small change that can give them enough security and support to shift stressful situations into moments of comfort and care. We met with Annie Gunning, CCLS, […]
Understanding Blood Gases: A Guide for Parents of Babies with HIE When your baby is diagnosed with hypoxic-ischemic encephalopathy (HIE), it can feel overwhelming to navigate the medical information and terminology. One term you may hear frequently in the neonatal intensive care unit (NICU) is “blood gases.” Understanding what blood gases are and why they are important can help you […]
Understanding the Role of MRI in Neonatal HIE When a newborn is diagnosed with Hypoxic-Ischemic Encephalopathy (HIE), parents often hear about a test called a MRI (Magnetic Resonance Imaging). This test is frequently used to evaluate the brain and guide care decisions, but it’s important to understand its benefits, limitations, and role in managing HIE. What is a MRI? MRI […]
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