Get Involved with the NEC Society

Learn how you can help the NEC Society build a world without necrotizing enterocolitis by sharing resources, joining programs, collarborating on research, advocating for NEC Awareness and more! 

Micah

20 ways to help us build a world without NEC

Share our resources created with the CHNC in your NICU

The NEC Society, in partnership with the Children’s Hospitals Neonatal Consortium (CHNC) NEC Focus Group, is proud to share resources on necrotizing enterocolitis (NEC) for NICU families and families impacted by NEC.

Diagnosed Resource Box

We have Family Resource Boxes with information for families affected by NEC. Materials in the box empower families so they can engage as the most important members of their baby’s care team.

If a baby has tragically passed away from NEC, we offer a bereaved family resource box that provides the information we wish we would have had when we lost our child.

Join the NEC Registry

The NEC Registry is a platform for patient-families impacted by NEC from around the world to share information about necrotizing enterocolitis

Micah who passed away from NEC
Micah, who tragically passed away from NEC

Share our storybook for bereaved families

Forever Our Little One is a storybook for bereaved families, written by NEC Society’s founder and Executive Director, Jennifer Canvasser, after she lost her little one, Micah, to NEC. 

For more resources for bereaved families, click here.

Leslie and Jennifer holding Forever Our Little One and a picture of Micah

Join our Research Incubator

With 175+ members, we are accelerating NEC research, by bringing together scientists & clinicians working in partnership with patient-families!

Join the Nurse Ambassadors

Nurse Ambassadors are committed to helping drive NEC research, education, and advocacy. Join our community of leaders to build a world without NEC.

Baby Micah and Nurse

May is NEC Awareness Month

We invite you to share how NEC has impacted your life and support the NEC Society by recognizing NEC Awareness Month.

Texas Milk Bank in NEC Awareness Shirts

Advocate for NEC Awareness Resolutions

Ten states and the United States Congress recognize May 17th as NEC Awareness Day or May as NEC Awareness Month.

New York recognizes NEC Awareness Day

Join us for the PAS NEC club!

The NEC Club at the Pediatric Academic Societies meeting brings together clinicians, pateint-families, and stakeholders to build a world without NEC through research, education, and advocacy. 

Champion a world without NEC

As an industry or nonprofit Champion, your organization is recognized as a dedicated partner to advancing research and advocacy to better understand, prevent, and treat necrotizing enterocolitis (NEC).

exhibitor floor

Run for a world without NEC

Join us in making a difference! Over 100 dedicated individuals have already run 26.2 miles to honor families affected by NEC. We’ve had advocates host countless community walks and events for the NEC Society, and people from across the globe proudly wear the NEC Society jersey.

We want YOU to be part of the movement. Join us in moving for a world without NEC.

Women running a relay race together for a world without NEC

Become a recurring donor

Recurring donations help to ensure that the NEC Society has the capacity to expand our reach and impact every month. 

Luna
Luna, who tragically passed away from NEC

Host an event to raise support

Every event, from family benefits and walks to runs, golf outings, galas, dinner parties, barbecues, bake sales, garage sales, and beyond, plays a vital role in advancing the NEC Society’s mission. 

Collaborate with us on research projects

Ensure your research is prioritizing patient-centered solutions by collaborating with the NEC Society on your research projects. 

Contact Erin Pryor, the NEC Society’s Research Director, erinpryor@NECsociety.org, to learn more. 

Misty in Bio

Invite us to present at your institutions

Connect your community to the NEC Society and stay up-to-date on the latest NEC research, educaiton, and advocacy by inviting the NEC Society to present at your instituion. 

Contact Erin Pryor, the NEC Society’s Research Director, erinpryor@NECsociety.org, to learn more. 

A woman speaks at a podium in front of a large screen displaying the NEC Society logo and images of premature infants, families, and candles.

Invite us to contribute to your publications

The NEC Society’s Scientific Council and Board is comprised of gobal experts in the NEC community.

To collaborate with us on publications, contact Erin Pryor, the NEC Society’s Research Director, erinpryor@NECsociety.org, to learn more. 

Co-Chair the 2027 NEC Symposium

The NEC Symposium is the world’s largest meeting dedicated to NEC.

Contact Jennifer Canvasser, the NEC Society’s founder and Executive Director, Jennifer@NECsociety.org, to learn more. 

Write an article for our website

Help us build a world without NEC by writing an article for the NEC Society’s news page on a topic that would benefit the NEC community. 

Contact Sarah Piephoff, the NEC Society’s Communications Manager, Sarah@NECsociety.org, to learn more. 

Invite us to attend your conferences

Invite us to share our resources and latest updates at your conferences to build a world without NEC!

Contact Sarah Piephoff, the NEC Society’s Communications Manager, Sarah@NECsociety.org, to learn more. 

Share your story

We share stories to show how real families and clinicians are affected by this devastating disease. Our stories demonstrate the urgency of our mission.

Lyddia holding her son Rexton
Lyddia and her son Rex, who tragically passed away from NEC