Care without barriers
Advance timely access to knowledgeable providers, comprehensive treatment and lifesaving therapies—regardless of ZIP code, income or insurance status.
Advocacy • Equity • Action
We advocate for a future where every person living with sickle cell disease is heard, believed and able to receive the care they deserve.
Awareness opens the door.
Advocacy changes what happens next.The change we’re building
People living with sickle cell disease face more than a complex inherited blood disorder. Too often, they also confront fragmented care, provider shortages, harmful bias and systems that were not designed around their needs.
We turn lived experience into public action—bringing patients, families, clinicians, researchers, community leaders and policymakers to the same table.
See what we stand forOur advocacy agenda
We center the voices of people with lived experience and pursue changes that are practical, equitable and lasting.
Advance timely access to knowledgeable providers, comprehensive treatment and lifesaving therapies—regardless of ZIP code, income or insurance status.
Champion education and resources for clinicians, emergency teams, educators and community health workers who support people living with sickle cell disease.
Support inclusive clinical research, clear trial education and equitable access to innovations that improve quality and length of life.
Confront stigma, bias and the dismissal of pain in hospitals, schools, workplaces and public policy.
Your voice has power
Whether you have two minutes, a platform or a partnership to offer, there is a meaningful way to stand with the sickle cell community.
Ask elected leaders to protect access, fund research and strengthen the sickle cell care system.
Find your elected officialsUse your voice to replace misinformation with understanding and move your community to action.
Visit the education centerBring your organization, expertise or resources into a growing coalition for better outcomes.
Partner with usThe movement includes you