Looking for resources during the pandemic?
Join us for monthly virtual educational webinars
with local and national sickle cell experts.
Sat May 30 - CLICK HERE TO REGISTER
Sat June 27 - REGISTRATION NOT YET OPEN
Sat July 25 - REGISTRATION NOT YET OPEN
Sat Aug 22 - REGISTRATION NOT YET OPEN
TENTATIVE! Sat June 20, 2020 - 3rd Annual Walk-4-SickleCell Fundraiser
TENTATIVE! Sat July 11, 2020 - Family Fun Day @ Roller Garden (more info to come...)
Sat Sept 12, 2020 - 3rd Annual Sickle Cell-ebration of Hope Gala & Fundraiser
Sickle Cell Foundation of Minnesota (SCFMN) was founded in 2015. We are a community-based organization comprising of passionate patients, caregivers, sickle cell trait carriers, healthcare providers, advocates, and other individuals and stakeholders who are concerned with the outcomes of our community.
Our Mission: To improve the quality of life for individuals and communities affected by sickle cell disease and sickle cell trait. Our goal is to provide community programs and resources that meet the needs of individuals and medical providers.
Our Vision & Values: By connecting individuals and families living with sickle cell to one another, to competent and compassionate medical providers and services that provide increased access to resources that address barriers to care, we believe we can and will help to improve health outcomes that also improve and enhance quality of life. Our commitment to the sickle cell community is deeply rooted in our belief that we are stronger together than as one. We value our individual and community health, equitable access to competent and compassionate care and community-centered solutions. The foundational pillars of our work create the building blocks necessary to increase health literacy, build support networks, and empower individuals to live at their full capacity.