MD Archives - NORD (National Organization for Rare Disorders)

NORD Publishes Report on Post-Transplant Lymphoproliferative Disease

Written by Laura Mullen on November 29, 2018

Washington, DC, November 29, 2018–As part of its ongoing series to promote awareness and education regarding rare diseases, the National Organization for Rare Disorders (NORD) has published a report on Post-Transplant Lymphoproliferative Disease (PTLD) in its Rare Disease DatabaseRead More

NORD Receives Grant from Anthem Foundation for Expansion of Rare Disease Database®

Written by Laura Mullen on September 25, 2018

Washington, D.C., September 25, 2018 – The National Organization for Rare Disorders (NORD) announced today it is enhancing its Rare Disease Database which serves as a valuable source of information for patients, families and caregivers in need of easy to understand language on rare diseases that are frequently… Read More

Archives for: November 29th, 2018

NORD Publishes Report on Post-Transplant Lymphoproliferative Disease

Written by Laura Mullen on November 29, 2018

NORD Receives Grant from Anthem Foundation for Expansion of Rare Disease Database®

Written by Laura Mullen on September 25, 2018

Alone we are rare. Together we are strong.®