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ONLINE REGISTRATION IS NOW CLOSED. Please register on-site.
TARGET AUDIENCE
Physicians, Nurses, Nurse Practitioners, Residents, Medical and Nursing Students, Physician Assistants, Social Workers and other Allied Health Practitioners involved in the care of patients with sickle cell disease, thalassemia and associated iron overload.
LEARNING OBJECTIVES
By attending this activity, participants will be able to:
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Describe new evidence in curative therapy for sickle cell disease and thalassemia.
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Discuss optimal approaches to diagnostic and genetic testing in hemoglobinopathies.
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Apply current evidence in prevention and treatment of stroke and thrombosis in hemoglobinopathies.
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Manage complex cases, including iron overload, non-transfusion dependent thalassemia and sickle cell disease.
PLANNING COMMITTEE
Madeleine Verhovsek, BSc, MD, FRCPC (Chair)
Associate Professor, Division of
Hematology and Thromboembolism,
McMaster University
Uma Athale, MD, MSc, FAAP, FRCP(C)
Associate Professor
Department of Pediatrics
McMaster University
Jennifer Wolfenden, RN
McMaster Haemoglobinopathy Clinic
Hamilton Health Sciences
Linda Waterhouse, BA, BSW, MSW, RSW
Social Worker
Pediatric Hematology/Oncology
Hamilton Health Sciences
Colleen Johnson, MN, NP (Adult)
Red Blood Cell Disorder Clinic
Toronto General Hospital
Karen Charpentier
Clinical Nurse Specialist
Hospital for Sick Children
Colin Yee, MD, FRCPC
Adult Hematologist
Grand River Hospital, Kitchener Waterloo
Sheilah Laffan
CHSE Program Manager
Continuing Health Sciences Education
McMaster University, Hamilton, ON
Shawn Locke
CHSE Coordinator
Continuing Health Sciences Education
McMaster University, Hamilton, ON