Trusted Resources: People & Places
Healthcare providers, researchers, and advocates
Sickle Cell Foundation of Minnesota (SCFMN) is the only active sickle cell community-based organization in the state of Minnesota. We are also a 501(c)(3), not-for-profit organization. It aims at improving the lives of individuals and communities affected by sickle cell disease through education, advocacy, access to resources, and community empowerment.
SCFMN is passionate about making a change and leaving our footprint wherever we go. We recognize that there are unmet needs in Minnesota’s sickle cell community and we want to be a source of strength, hope, and encouragement to those in need of our services.
We also recognize the impact of providing reliable education and awareness around sickle cell disease and sickle cell trait. We regularly partner with other community organizations, hospitals, clinics, and businesses so that we can increase our reach and impact more communities.
Related Content
-
Cynthia Gipson, MACynthia Gipson is a family advocate for ...
-
Patient-reported experience measure in sickle cell diseaseObjectives: To develop patient-reported...
-
Here Are Ways to Help Friends With Sickle Cell DiseaseWhenever I meet new people and tell them...
-
Simone C. Eastman Uwan, MDDr. Simone Eastman Uwan was born in Guya...
-
Strategies to Avoid the FluIt’s cold and flu season and the usual...
-
SCD Clinical Trials Network Workshop – Washington, DCJoin us for an afternoon of fun acti...
-
Metropolitan Seattle Sickle Cell TaskforceThe Metropolitan Seattle Sickle Cell Tas...