The PNH Research and Support Foundation is dedicated to funding research to find a cure and new treatments for Paroxysmal Nocturnal Hemoglobinuria (PNH) and to helping PNH patients in need with funding for disease-related expenses not covered by insurance.
As "Patient Partner" organizations, the PNH Foundation and AA&MDSIF work closely to make patient education and support services available to PNH patients and their families. Be sure to visit their Web site for additional support information for PNH patients and families.