The Jefferson car seat and Hope car bed are such amazing pieces of equipment for these special kiddos. Because of their specialized nature, it’s very expensive ($1300-$1800) and unfortunately adds a financial burden on families where many insurances won’t cover it.
Our program helps make this easier by helping those with an available car seat get in touch with those who need one. O Warrior will help with the cost of shipping car seats when families need the help.

Sometimes all we need is community. People who know what we’re going through, can hug us, talk to us, and walk with us. We’re working hard to create that community for O families with our monthly support groups. Watch out for future events like 5Ks and gatherings.

We are actively looking for community outreach volunteers in all 50 states. If you are interested in helping, reach out to us at hello@owarrior.org.

We’ve heard many stories about parents learning about their O Warrior’s diagnosis and not knowing where to turn for more information. Google searches can lead to concerning studies, and information received from MFM offices can be outdated. We have collected stories from O Warriors and their families around the world.

O Warrior would like to recognize the mothers of O Angels (deceased omphalocele child) by offering a keepsake in honor of their O babies.

If you are the mother of an O Angel or would like to nominate the mother of an O Angel to receive an O Warrior necklace, please complete the form below. Our hearts are with you, and we would love to send you a necklace to help you keep your O baby close to your heart.

O Warrior grants are to be used to assist current and future families dealing with an Omphalocele diagnosis. We provide financial assistance to those families to help with the costs associated with medical care, long distance travel, or special living arrangements. There are many extra costs that omphalocele families can be burdened with while ensuring their baby gets the proper care that they need.

Navigating the omphalocele diagnosis can be extremely overwhelming. We have put together educational resources for every step of the way: including initial diagnosis, MFM appointments, NICU stays, closure/repair surgery, and more.