Archives


Check out the NEC Society’s Inclusivity Statement

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Living With NEC: A Survivor’s Experience

Lakevia is grateful to have survived this terrifying disease but continues to live with its consequences- she shares her story.

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NEC Awareness Day (May 17)

As the COVID-19 crisis rages, we know that babies are still developing necrotizing enterocolitis (NEC). While many of our events have been canceled, we hope you’ll join us as we recognize World NEC Awareness Day on May 17.  NEC is…

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NEC Society Receives $450,000 Award from Chan Zuckerberg Initiative

The Necrotizing Enterocolitis (NEC) Society is one of 30 patient-led organizations to become part of the Chan Zuckerberg Initiative’s Rare As One Network. The Rare As One Network aims to support patient communities in accelerating research and driving progress in…

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NEC Society and Cincinnati Children’s Announce the NEC Symposium

Exhibitor registration is open and more details can be found in our prospectus by clicking here.  The NEC Society is honored to partner with Cincinnati Children’s Hospital Medical Center to present the Necrotizing Enterocolitis (NEC) Symposium, April 13-16, 2021 at…

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NEC Society Receives $250,000 Research Capacity Award

The NEC Society has received a $250,000 Engagement Award from the Patient-Centered Outcomes Research Institute (PCORI) to support the organization’s two-year research capacity building project. This PCORI award will advance the NEC Society’s ability to drive patient-centered outcomes research (PCOR)…

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NEC Symposium, 2019

2019 NEC Symposium Summary now available!

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NEC Society Shop is now open!

All proceeds go directly toward our mission to build a world without NEC!

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VIDEO: NEC Prevention Through Collaboration

Check out our new video designed to encourage providers and patient-families to partner to improve care for babies!

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NEC Society Biorepository

First ever NEC biobank established!

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