Online PNH Resources
The PNH Patient Community
The PNH Patient Community is a patient support site in partnership with National Organization for Rare Disorders (NORD) and the Aplastic Anemia & MDS International Foundation (AA-MDSIF). This site is dedicated to providing PNH patients access to other patients as well as many free events offered throughout the country.
NORD is dedicated to helping improve the lives of people with rare diseases through advocacy and by serving as a clearinghouse for news, information about research and grants, and patient services and resources.
AA-MDSIF is a nonprofit patient organization that serves as a resource for patient assistance, advocacy, and support. The organization supports research to find treatments and potential cures for aplastic anemia (AA), myelodysplastic syndromes (MDS), and related bone marrow diseases including PNH. The AA-MDSIF Web site provides educational materials and medical information about AA, MDS, and PNH.
On this site, you can search a collection of clinical studies being conducted by the NIH.
The PNH Research and Support Foundation is an organization dedicated to raising funds for PNH research and helping families with disease-related expenses not covered by insurance.
The PNH Support Group is an online network of over 400 individuals who are living with PNH, or care for someone with PNH, and who are willing to share personal experiences. Other resources include frequently asked questions, live chat forums, current news threads, a PNH glossary, key links, and educational materials.
On this site, healthcare professionals and others can review regularly updated information about federally and privately supported clinical research in human volunteers. This site also gives you the ability to research information about a trial's purpose, who may participate, locations, and contact information.
Contact a nurse case manager from OneSource™ who can provide information and useful tools to help you care for your patient with PNH.
Support scientific collaboration in the PNH community by helping offer the international community greater insight into an uncommon disease with potentially devastating consequences. Enroll your patients in the PNH Registry today.
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