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Simplemind map for sickle cell anemia series#
Simplemind map for sickle cell anemia free#

Simplemind map for sickle cell anemia free#

SCDC webinars, hosted by the SCDC program in California, are free and open to the public.

Spanish transcripts of the videos are available online. The videos share the stories of Kevin and Calvanay, two young adults with SCD, and their transition to adult care, how it has affected them, and how they’ve overcome challenges.

Simplemind map for sickle cell anemia series#

Stepping Up: A 2-part video series for teenagers and young adults with SCD.

Sickle Cell Trait Toolkit is a collection of fact sheets covering various health problems affecting people with sickle cell trait.

SCD resources are also available in Spanish at our SCD Spanish webpage.

SCD materials webpage has fact sheets and infographics on living well with SCD.

Watch the Minority Blood Donation video to learn about the importance of African American blood donors to people with SCD.

Provider and patient resources about blood transfusions and blood donations.Transfusion Complications Monitoring Publications.Educational videos on topics related to blood transfusions.This project aims to learn more about transfusion-related health problems and to identify ways to decrease these health problems to improve the health of people with SCD, thalassemia, and other red blood cell disorders.įind resources based on the Transfusion Complications Monitoring project: Some people with SCD and thalassemia may require blood transfusions to stay healthy, but, sometimes, they may experience health problems after receiving blood transfusions. The Transfusion Complications Monitoring project is a collaboration between CDC, Georgia State University, University of Florida, and the UCSF Benioff Children’s Hospital Oakland. Learn more about the Transfusion Complications Monitoring project. The Bloodline Newsletter is a quarterly e-newsletter providing updates about the SCDC Program.SCDC Policy Memo: Understanding Sickle Cell Disease: CDC’s Role in Surveillance, Education, and Awareness.Maps and Figures on SCDC Data by State – California and Georgia.The program will help inform policy and healthcare standards to improve and extend the lives of people with SCD. As more resources become available, CDC plans to expand the program to include additional states. Currently, Georgia and California are the states participating in the SCDC program. The SCDC program collects health information about people with SCD to study the long-term trends in diagnosis, treatment, and healthcare access for people with SCD in the United States. The SCDC program, which has been ongoing since 2015, is CDC’s current monitoring project.

Sickle Cell Data Collection (SCDC) program (ongoing since 2015).Public Health Research, Epidemiology, and Surveillance for Hemoglobinopathies (PHRESH) (from 2012-2014).Registry and Surveillance System for Hemoglobinopathies (RuSH) (from 2010-2012).Learn more about CDC’s SCD surveillance history through a fact sheet that allows you to compare each project using information about data sources, participating states, and accomplishments of each project.ĬDC coordinated these efforts as part of three projects: