Mission:
- To provide current information (both medical and holistic / integrative), resources, support groups, and events for Sickle Cell patients, their families, friends, and health care professions in order to empower and enhance quality of life.
Home Page:
The Sickle Cell Association of BC is always looking for members and volunteers. Please visit our members and volunteers section.
Covid-19 / Coronavirus updates and protocols for those with sickle cell:
THE COVID–19 PANDEMIC AND HAEMOGLOBIN DISORDERS
The Sickle Cell Association of BC is dedicated to providing families with the information they need to make educated
and informed decisions to improve the quality of life for those suffering from Sickle Cell Disease and their families.
and informed decisions to improve the quality of life for those suffering from Sickle Cell Disease and their families.
SCDABC is a member in good standing with the Sickle Cell Disease Association of Canada/ Association d’Anémie Falciforme du Canada (SCDAC/AAFC)
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We would like to thank ApoPharma for the support they gave so that we may share lectures on Sickle Cell research.
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Disclaimer:
Information or materials on this website or in any event the Sickle Cell Association of BC creates are not intended to treat or replace your doctor’s advice nor do we endorse any particular product, technique, or idea. It is highly recommended that patients contact their haematologists or health care provider for adequate care and treatment.
Information or materials on this website or in any event the Sickle Cell Association of BC creates are not intended to treat or replace your doctor’s advice nor do we endorse any particular product, technique, or idea. It is highly recommended that patients contact their haematologists or health care provider for adequate care and treatment.