News from NORD

MDS Foundation


 

Join the MDS Foundation for a Patient and Family/Caregiver forum on May 5, 2018, in Salt Lake City. This one-day forum provides new patients, long-term survivors, and caregivers the opportunity to learn from experts about treatments and strategies for living with MDS. More.

Recommended Reading

Medical Nutrition Equity Act Capitol Hill Day Planned for June 1
MDedge Neurology
NORD and Other Patient Organizations Oppose Short-Term, Limited-Duration Health Plans
MDedge Neurology
Running for Rare Team Participates in Boston Marathon to Raise Funds for Undiagnosed Patients
MDedge Neurology
NCATS Unveils Toolkit for Patient-Focused Therapy Development
MDedge Neurology
NORD Updates Educational Rare Disease Reports
MDedge Neurology
American Partnership for Eosinophilic Disorders (APFED)
MDedge Neurology
Children’s Cardiomyopathy Foundation
MDedge Neurology
Cornelia de Lange Syndrome (CdLS) Foundation
MDedge Neurology
Dup 15q Alliance
MDedge Neurology
International Pemphigus and Pemphigoid Foundation
MDedge Neurology