We provide families of children with feeding tubes a path towards joyful, relaxed, independent oral eating while offering the support needed throughout the process.

Request a "pouch" to keep your child's medical history, appointment schedule, etc. in one place.

Hope for HIE connects, supports and advocates on behalf of the global HIE community working to improve the quality of life of children and families impacted by neonatal and pediatric-acquired Hypoxic Ischemic Encephalopathy, across the full range of outcomes and impacts.

The NEC Society is a 501(c)(3) nonprofit organization dedicated to building a world without necrotizing enterocolitis (NEC) through research, advocacy, and education.

We provide vital guidance and assistance to parents of a child with cerebral palsy, including education and information about financial assistance.

The Mighty is a health care company created to empower and connect people facing health challenges and disabilities.

Resources, Shop, and Community Support.

Down Syndrome Support Network

To advance the diagnosis, treatment, and prevention of congenital heart defects (CHDs) by funding the most promising research.

Education and resources regarding CDH.

Community, education, support for parents of children with visual impairments.

Podcast for Medically Complex Parenting

Creating tools and solutions to empower every child and family facing medical experiences.

This information packet contains tips for getting care, understanding signs and symptoms of illness, medicines and immunizations, managing breathing problems, and feeding.

Mighty Miracles Foundation is to empower and support families of preemies and others with special health needs beginning life in the Neonatal Intensive Care Unit (NICU). We do this by sending out free care packages to families currently going through the NICU and by partnering with NICU to provide items from our care packages for their families.