Our Mission
Sick Cells’ mission is to elevate the voices of the sickle cell disease (SCD) community and our stories of resilience. In highlighting the grave disparities our community faces, we will influence decision-makers and propel change.
Sick Cells’ mission is to elevate the voices of the sickle cell disease (SCD) community and our stories of resilience. In highlighting the grave disparities our community faces, we will influence decision-makers and propel change.
Ambassador Program
Our diverse network of sickle cell ambassadors meet regularly to discuss the community’s needs, how to best educate our peers, and how to engage in policy at all levels. Learn More
Faces of SCD Storytelling Program
There’s no one face or “look” of SCD, and we’re determined to highlight all of the beauty, challenges and diversity within the community. Learn More
public interest making sickle cell a public health concern
SCD, which is a relatively invisible disease that affects people of many races and ethnicities
the general public, who do not typically recognize their day-to-day encounters with SCD, to advocate for SCD
policy makers, educators, employers, healthcare administrators and healthcare providers to act to improve treatment and care for the SCD population
research and drug development which will lead to better treatments
the sickle cell community, regardless of hemoglobin type, to share their stories and know that they are not alone
Through these actions, we hope to improve the quality of life and care for people living with the most common genetic disorder by challenging current policy and shifting social norms.