Written by Jennifer Canvasser, founder and executive director of the NEC Society

When my son Micah was six weeks old, I thought he had overcome his fiercest battles that are common to babies born at 27 weeks gestation. He had doubled his birth weight, was beginning to nurse, and looked like he would be discharged home in just a couple of weeks.

Tragically, like a phantom menace on steroids, Micah developed necrotizing enterocolitis (NEC). His infection led to a host of complications including multiple bowel resections, and most significantly, renal failure. Micah became severely fluid overloaded, to the point where he couldn’t even open his eyes.

Thanks to an incredible team of providers, Micah survived and came home. After spending months in the NICU and PICU, having Micah at home was a dream come true. Micah had made it, and we could finally begin to have a more “normal” life.

Tragically, Micah died just before his first birthday from complications of NEC. It’s been six years since I kissed Micah goodbye. I have spent every one of those days since then working to keep Micah in my life. Through this journey, I have gained perspective and insight that I desperately wish I had known before Micah’s NEC diagnosis.

Many families impacted by NEC have one thing in common: they learn about NEC for the first time when their child is being diagnosed. The shame and guilt I experienced from not knowing about NEC or the risks – and thus not being able to advocate for Micah – was overwhelming. As parents, we are compelled to protect the health of our babies, but tools for early detection and strategies for NEC prevention are underdeveloped or non-existent. Accordingly, NEC often blindsides both clinicians and families.

With the NEC Society’s leadership, we are making more progress than ever. Still, NEC awareness, resources, and research are inadequate because prevention was neglected for decades, and the disease remains too often regarded as inevitable. The NEC Society is working tirelessly to build a world without NEC.

May 17 is World NEC Awareness Day. As the world’s leading NEC-focused nonprofit, we are bringing our community together to raise awareness and drive research. There are 9 things we want the world to know about this devastating, multifactorial disease:

1. NEC is the most common cause of death in hospitalized premature infants after two weeks of age. Babies born prematurely or with a complication, like congenital heart disease, are most at risk of NEC. In the US, thousands of babies develop NEC and hundreds of babies die every year from this complex intestinal condition.
2. NEC causes a severe inflammatory process that can lead to intestinal tissue damage and death. Once NEC is diagnosed, many babies only live for a few hours or days. Surgery for NEC is not curative and the babies who survive often have lifelong neurological and nutritional complications.
3. Mothers milk is one of the best ways to help prevent NEC in medically fragile babies. When mothers own milk is unavailable, pasteurized donor milk is the next safest option for babies at risk of NEC.
4. Formula does not protect against the risk of NEC in medically fragile babies. For babies at risk of NEC, mothers own milk and pasteurized donor milk are protective against NEC, while formula feeding is not protective against this risk.
5. While we cannot eliminate the risks of NEC (yet), prevention measures are effective. While there are no ways to cure NEC, research has shown promising ways to reduce the risks, including mother’s milk (or donor milk), standardized feeding protocols, probiotics, limiting antibiotics, and having NICUs participate in quality improvement projects.
6. Parents must be trusted and valued as the most important member of their baby’s care team. Parents know their babies best. Check out the NEC Society’s resources on how healthcare providers can partner with NICU parents.
7. Term infants can develop NEC. NEC is not only a disease of prematurity. We have very little data to help us understand how and why NEC occurs in term-babies.
8. There are disparities and variation in care for babies at risk of NEC. Without universal standards of care or guidelines, the type of care a baby receives varies from center to center, and even from clinician to clinician. We’re working to change this.
9. We’re making more progress than ever before. We have seen more resources dedicated to building a world without NEC in the last five years than we have in the last five decades.

Join us for NEC Awareness Month!
We encourage you to show us how NEC has impacted your life. We are asking families ot share their stories, and NEC clinicians and scientists to highlight their care teams and labs that work tirelessly to prevent NEC. Join us on social media and use the hashtags #preventNEC #NECday 

Learn more about how we’re building a world without NEC and make a donation in honor of a baby impacted by the disease at NECsociety.Kindful.com

The NEC Society is a 501(c)(3) organization dedicated to driving research and improving outcomes for medically fragile babies at risk of necrotizing enterocolitis. The NEC Society brings together patient-families, clinicians, scientists, and other diverse stakeholders committed to building a world without NEC.