Trusted Resources: People & Places
Healthcare providers, researchers, and advocates
Sickle Cell Alliance Foundation
6225 Colerain Ave., Suite BCincinnati, Ohio, United States
Email Phone Web
Launched in May 2014, Sickle Cell Alliance Foundation is a passionate non-profit, community-based organization. It is committed to being a valuable resource to guide and help families and patients – children, teens and adults – living with the life-threatening sickle cell disease. It’s goal is to ensure the appropriate programs and needed resources are available and offered to the patient and caregiver.
Through the strong connection with the families, Sickle Cell Alliance Foundation will be “their voice”. This will help as they advocate, partner and develop relationships with hospitals, schools, companies and public officials. This will help to heighten awareness and raise the much-needed funding to educate at the local and national levels to improve care.
Related Content
-
Sickle Cell Disease in the Emergency Department: Confronting Barriers to Care“You’re too pretty to have a disease...
-
Inaugural Event, World Cord Blood Day 2017, Highlights Non-Controversial Source of Stem CellsWorld Cord Blood Day (November 15th) wil...
-
Self‐Management Recommendations for Sickle Cell Disease: A Content Analysis of WebsitesThis paper reports on the findings of a ...
-
Is Your Child the Right Candidate for Hydroxyureahttps://www.youtube.com/watch?v=vMvC5rVH...
-
Hydroxyurea Shows Clinical Benefit without Alteration of Fetal Hemoglobin, MCV, or Hemoglobin in Unselected Adult an...Introduction: Sickle cell anemia is the...
-
Gaurav Kharya MBBS, DNB, DCHDr. Gaurav Kharya is a Clinical Lead at ...
-
Lakshmanan Krishnamurti, MDDr. Krishnamurti graduated from the Arme...
+myBinder