Alberta (Canada) Porphyria Society
  • Home
  • What's New
  • Information about Porphyria
    • Guide to Porphyria
    • Types of Porphyria
    • Drug Safety Databases
    • EPP
    • Laboratory Investigation of the Porphyrias
    • Canada - Reported Cases of Porphyria
    • Prevalence
  • About Us
    • Alberta Porphyria Society
    • Support for Canadians with Porphyria
    • Network of Rare Blood Disorder Organizations
  • Support
    • Peer to Peer Support
    • International Porphyria Organizations
    • Rare Connect
  • Research
    • Research in the USA and Canada
    • Research - International
  • Resources
    • Orphanet
    • Mobile Web App for the Safe/Unsafe Drug List for the Acute Porphyrias
    • Patient's and Doctor's Guide to Medication in Acute Porphyria
    • Medicalert Canada
    • 2013 International Porphyria Conference
  • How To Help
    • Become A Member
    • Donate
    • Volunteer
  • Past Events
    • 2014, March 26th - 1st Annual Hope Jam
    • 2014 Annual General Meeting
    • Porphyria Patient Education Workshop June 23, 2013
    • Rare Blood Disorders Education Day March 9, 2013
    • 2013 Annual General Meeting and Information Sharing
  • Our Sponsors
  • Our Partners
  • 2015, 2nd Annual Hope Jam

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Network of Rare Blood Disorder Organizations (NRBDO) www.nrbdo.ca

Representatives of the Alberta Porphyria Society have been included in the NRBDO since 2010 even though porphyria is not a rare blood disorder. The members of this coalition support one another in their quest to provide better health care for the members of their organizations.
The Network of Rare Blood Disorder Organizations is a coalition of national patient groups, formed to share the best practices in health care delivery for people with rare blood disorders such as hereditary angioedema; aplastic anemia, Fanconi anemia, paroxysmal nocturnal hemoglobinuria (PNH), and myelodysplasia; primary immune deficiency; porphyria, sickle cell disease, thalassemia, thrombotic thrombocytopenic purpura (TTP), hemophilia and von Willebrand disease. They work, advocate and lobby together in a coordinated fashion on key issues to secure and maintain patient access to comprehensive care while empowering patients who have rare blood disorders. The goals of the network are to ensure that finite health care dollars are spent rationally so as to promote the health of our citizens, reduce pain and suffering, and help people to live as nearly normal lives as possible and to raise the level of awareness and knowledge of the patient groups’ roles in the following key issues:
  • Importance of patient registries to facilitate access to quality care and existing and emerging therapies
  • Advantages of specialized care centers for complex rare disorders
  • Improved access to drug therapies
  • Tracking of blood and blood products to permit inventory management and effective recall and notification procedures
  • Need for active adverse reaction reporting and post-marketing surveillance of therapies used to treat these disorders
  • Treatment guidelines
  • Educational guidelines to maintain same level of education across Canada
  • Orphan drug legislation
  • Conferences: 
            2006: Comprehensive Care for Rare Blood Disorders Conference
            2009: Progress in Comprehensive Care for Rare Blood Disorders Conference -- Presented by CSL Bering
            2011: NRBDO - Alberta: Awareness and Education Day -- held in Edmonton, Alberta

CONTACT INFORMATION:

Network of Rare Blood Disorder Organizations
C/O Canadian Hemophilia Society
National office in Montreal
400-1255 University Street
Montreal, QC  H3B 3B6
Tel.: 514-848-0503
Toll-free: 1-800-668-2686
Fax: 514-848-9661
E-mail: nrbdo@hemophilia.ca

Website: www.nrbdo.ca
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