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THE MORGAN LEARY VAUGHAN FUND PROVIDES UPDATE ON NATURAL HISTORY REGISTRY FOR NECROTIZING ENTEROCOLITIS

Naugatuck, Connecticut, October 3, 2017—The Morgan Leary Vaughan Fund (Morgan’s Fund) today announced that three new surveys are open on the Natural History Registry for Necrotizing Enterocolitis (NEC Registry). The surveys encompass the neonatal (newborn) period, feeding, and Necrotizing Enterocolitis (NEC) diagnosis and treatment.

The NEC Registry is a collaborative effort between Morgan’s Fund and the National Organization for Rare Disorders (NORD) to study NEC. Morgan’s Fund was selected by NORD to create the NEC Registry as part of a cooperative project between NORD and the U.S. Food and Drug Administration that supports research on rare diseases and how they progress over time—natural history studies.

OVERVIEW OF RESEARCH STUDY

The NEC Registry is more than a versatile online system that securely collects and stores data for medical research; it is a dynamic participant-driven resource that can empower and unite the NEC community through shared knowledge. Registry participants not only can complete surveys about their own disease experiences, but also can learn about other participants’ experiences by viewing aggregated survey data. As the registry sponsor, Morgan’s Fund ensures that data privacy and confidentiality are strictly maintained. Participation in the NEC Registry is free and voluntary, and participants may withdraw at any time.

COMMUNITY INVOLVEMENT

The NEC Registry is a powerful opportunity for individuals with NEC and their family members to contribute directly to research that will enhance our understanding of NEC, thus facilitating the development of new diagnostic and treatment options for the NEC community. Participation is especially vital given the rarity of NEC—every patient experience is a unique and invaluable part of the natural history of NEC.

For more information or to join, visit NECregistry.org

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About Necrotizing Enterocolitis

Necrotizing Enterocolitis (NEC) is a rare, inflammatory disease that leads to necrosis (death) of the intestine. It is predominately due to prematurity and its statistics are startling. NEC is the second leading cause of death in premature infants. NEC is the 8th leading cause of death during the newborn period (the first 28 days of life). NEC affects about 9,000 of the 480,000 infants born preterm each year in the United States. All newborn infants born preterm or born with a low birth weight (less than 5.5 pounds) are at increased risk for NEC. The smaller the infant or the more premature the delivery, the greater the risk.

(Sources: UC Davis Health System, CDC/NCHS, and NICHD.)

About The Morgan Leary Vaughan Fund

The Morgan Leary Vaughan Fund emerged (Morgan’s Fund) from a need to establish a mechanism for:

  • Disseminating credible and timely information about NEC to parents whose infants are most at risk for developing NEC
  • Raising the level of public awareness about NEC and the potentially devastating effects it can have on infants and their families
  • Advancing research to prevent, diagnose, treat, and ultimately, cure NEC

Currently, it is headquartered in Naugatuck, Connecticut and has a satellite office in Austin, Texas.

About NORD
NORD, a 501(c)(3) organization, is a patient advocacy organization dedicated to individuals with rare diseases and the organizations that serve them. NORD, along with its more than 250 patient organization members, is committed to the identification, treatment, and cure of rare disorders through programs of education, advocacy, research, and patient services.

CONTACT: Mary L. Midolo, Registry Administrator, NECregistry@morgansfund.org or +1 (203) 606-4873

THE MORGAN LEARY VAUGHAN FUND LAUNCHES FIRST NATURAL HISTORY REGISTRY FOR NECROTIZING ENTEROCOLITIS

Research study is open to participants worldwide to advance understanding and treatments for rare disease that leads to necrosis (death) of the intestine.

Naugatuck, Connecticut, January 9, 2017—The Morgan Leary Vaughan Fund (Morgan’s Fund) has launched the first natural history registry for Necrotizing Enterocolitis (NEC)—an inflammatory disease that leads to necrosis of the intestine. NEC currently has no cure.

“The Natural History Registry for Necrotizing Enterocolitis (NEC Registry) will provide a complete picture of each patient’s experience with NEC,” said Stephanie M. Vaughan, Co-founder and President, Morgan’s Fund. “The NEC Registry is a platform for every baby (be they living or deceased), every family affected by NEC to help shape future research in NEC. It is a unique opportunity to drive this research to answer their unanswered questions and find a cure.”

To drive awareness and participation, Morgan’s Fund will promote the registry via mass media. Morgan’s Fund will target patients and their families or caretakers, and relevant NEC experts including neonatologists, clinicians and researchers.

“Our goal is to enroll as many patients, or their parents or legal guardians, as possible,” said Ms. Vaughan. “The success of the registry is dependent upon community participation.”

The NEC Registry is a natural history study registry that consists of electronic surveys to collect information about the patient experience and disease progression. Patients, or their caregivers or guardians can enter information from anywhere in the world. The data is made anonymous and stored securely in an online portal called a registry. Morgan’s Fund may share the data but not your personal identifying information with individuals or institutions conducting research or clinical trials, as approved by the study’s governing board that includes scientists, doctors and patient advocates.

Morgan’s Fund is launching the NEC Registry in collaboration with the National Organization for Rare Disorders (NORD), an independent charity that built its natural history study platform as part of its mission to help identify and treat all 7,000 rare diseases. Funding is supported by a cooperative agreement between NORD and the U.S. Food and Drug Administration (FDA). The FDA has praised NORD’s program as a helpful tool “that protects the security and privacy of personal information, while making valuable information available to a researcher or drug developer interested in creating a new therapy for a rare disease.”

NORD President and CEO Peter L. Saltonstall said, “NORD’s natural history studies platform empowers patients and families to drive research and eliminate some of the unknowns that still exist in rare diseases. We are glad to be working with our Member Organization on this project and thank the FDA for its support and ongoing commitment to help people with rare diseases.”

  • NEC is a rare disorder that is predominately due to prematurity.
  • NEC is the second leading cause of death in premature infants.
  • NEC is the 8th leading cause of death during the newborn period (the first 28 days of life) in the United States.
  • NEC occurs in approximately 25,000 American babies per year.

For more information, visit NECregistry.org

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About The Morgan Leary Vaughan Fund

The Morgan Leary Vaughan Fund (Morgan’s Fund) is an all-volunteer, public charity dedicated to Necrotizing Enterocolitis (NEC). Its mission is to promote public awareness about NEC and the potentially devastating effects it can have on preemies and their families, and to advance research to prevent, diagnose, treat, and ultimately, cure NEC. Named after Morgan, it celebrates his survival, courage and strength.

Morgan and his twin brother were born at 28 weeks, one day gestation—nearly three months early— each weighing less than 2.5 pounds. At four days old, Morgan developed NEC and lost approximately
20% of his small intestine. Morgan not only survived but also has thrived since his bout with NEC. This is his family’s way of paying it forward. Morgan’s Fund is a proud member of the National Organization for Rare Disorders and the Preemie Parent Alliance.

About National Organization for Rare Disorders (NORD)

An independent 501(c)(3) nonprofit organization, NORD is the leading advocacy organization representing all patients and families affected by rare diseases in the U.S. Established in 1983,
NORD is committed to the identification, treatment and cure of the 7,000 rare diseases that affect 30 million Americans, or 1 in every 10 people, through programs of advocacy, education, research,
and patient/family services. In addition to educational resources for patients, families, medical professionals and students available on its website (www.rarediseases.org), NORD represents
250 member organizations and collaborates with many others in specific causes of importance to the rare disease patient community.

Contact: Mary L. Midolo, Registry Administrator, NECregistry@morgansfund.org or +1-203-606-4873

  1. Woodcock, J. “The more we know about rare diseases, the more likely we are to find safe and effective treatments.” FDAVoice (Oct. 23, 2014)
  2. UC Davis Health System. Newsroom. All Probiotics Are Not the Same in Protecting Premature Infants from Common, Life-threatening Illness.
    UC Davis Health System. University of California, Davis, Health System, 17 Oct. 2013. Web.
  3. Heron M. Deaths: Leading Causes for 2012. Nation vital statistics reports; vol 62 no. 10. Hyattsville, MD: National Center for Health Statistics. 2015.
  4. “Necrotizing Enterocolitis (NEC).” www.pediatricsurgerymd.org. The American Pediatric Surgical Association. n.d. Web. 24 January 2016.
    <http://www.pediatricsurgerymd.org/AM/Template.cfm?Section=Conditions&template=/CM/ContentDisplay.cfm&ContentID=4298>

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