SCAGO
The SCAGO supports individuals and families affected by Sickle Cell Disease (SCD). We offer advocacy, education, and resources to improve quality of life, reduce stigma, and promote equitable healthcare access across Ontario.
COMMUNITY IMPACT PROGRAMS
ADVOCACY:
We provide system level advocacy on behalf of people affected by SCD in schools, workplaces, hospitals, and at the different government levels.
EDUCATION:
We provide accredited E-Course to healthcare providers to ensure people living with SCD receive equitable, quality care in Ontario hospitals. We also offer disease management education to affected families.
RESEARCH
We conduct research and support emerging studies in partnership with health agencies and academic institutions to improve SCD care.
AWARENESS
We host and attend awareness campaigns, events, and workshops to educate the public, engage communities, and share lived experiences of those with SCD.
DIRECT SUPPORT SERVICES
PEER SUPPORT
Join peer support groups virtually or in-person for patients or families across Ontario.
COUNSELLING
Free short-term counselling (2–3 sessions) by phone or online for individuals and caregivers.
PATIENT WELLBEING COORIDINATORS
Patient Wellbeing Coordinators provide direct support to individuals living with SCD in navigating optimal hospital care and in accessing community services and social supports.
SCHOLARSHIPS & GRANTS:
$2,000/year in Sunday Afolabi Scholarship to eligible students and up to $500/year in emergency support for SCD-affected families.
DOWNLOAD OUR SERVICES PDF
Articles
