Evidence-based, patient-informed, culturally grounded.
BHASNet partners with healthcare professionals, researchers, and policy bodies to improve outcomes for people living with sickle cell disease and related blood disorders in Saskatchewan.
Patient-experience-informed training.
We work directly with healthcare professionals to build culturally responsive, patient-informed knowledge and best practices for managing sickle cell disease and other blood disorders.
Research grounded in lived experience.
As a grassroots organization centering patient and caregiver voices, we offer a direct line to community insight that strengthens research design and policy relevance.
Where clinical and research partnerships fit in.
Training & education sessions
Deliver or co-develop workshops for healthcare staff on culturally responsive sickle cell and blood disorder care.
Research partnerships
Collaborate on data-informed studies and treatment approaches, with direct access to community-grounded insight.
Policy & advocacy collaboration
Support inclusive health policy work and disability incentive advocacy with clinical and research expertise.