WHAT WE DO

 

Advocacy: arguing the case for people affected

Raising Awareness of the hereditary causes of sickle cell disorder

Counselling: providing unbiased factual information to enable informed decision making

Data collection (quality of population of data-base)

Surveillance and Research(engagement of local health service agents)

Community education and partnerships (formation of local Sickle Cell Clubs)

Outreach work and workshops to inform, educate and support people and communities