Rare Disease Day is February 28th. Ask any NICU parent or healthcare provider and they are likely to tell you that NEC is not rare in the NICU. NEC affects thousands of premature and medically fragile infants every year. Indeed,…
Read MoreMore than 50 clinical trials on probiotics and necrotizing enterocolitis (NEC) have been published, prompting some medical organizations to provide guidance and recommendations on the use of probiotics with infants who are at increased risk of NEC. As the NEC…
Read MoreLike each of us, the NEC Society began 2020 with specific plans, goals, and a vision for the possibilities of 2020. Of course, our best-laid plans were promptly upended when the pandemic swept across the country. Undoubtedly, this year has…
Read MoreBefore the pandemic, the NEC Society completed the California International Marathon (CIM) each year in honor of babies affected by NEC and to raise funds and awareness to advance our mission. We’re hosted a virtual Charity Run/Walk on December 12…
Read MoreWritten by Jennifer Canvasser, founder and director of the NEC SocietyThis originally appeared on GlobalGenes.org My son Micah spent months in the NICU and PICU. During his hospitalization, I learned what it means to be vulnerable, isolated, and powerless. It…
Read MoreOur Fall 2020 Webinar Series attracted more than 700 registrants from over 70 countries. Links to the recordings and slides are available below. Please join our email list to stay tuned for our 2021 webinars and virtual sessions! Lessons From…
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