Google
Trusted Resources: News & Events
Latest announcements and gatherings
P.O.W.E.R ECHO Project Community Health Worker (CHW) Training
Cost: Free
Monthly sessions
12–1 p.m. EST
Zoom online training
The P.O.W.E.R ECHO Project Community Health Worker Training is designed to assist community health workers with resources and education, in order to strengthen their efforts in providing support services for sickle cell disease (SCD) patients. P.O.W.E.R ECHO Project uses the ECHO telecommunication model to reach community health workers by offering online training services on emerging and current topics in sickle cell disease.
The P.O.W.E.R. training for Community Health Workers (CHWs) is designed to provide CHWs working in the SCD community with further resources and educational tools to strengthen their efforts in providing supportive services for sickle cell disease patients and their families.
The P.O.W.E.R ECHO Project uses the ECHO telecommunication model to bridge CHWs from various regions in professional development sessions focused on current and emerging sickle cell disease topics through training and case study discussions.
Upcoming Session:
October 12, 2023 | 12:00 – 1:00 PM EST
Topic: Bridging the Gap – Patient and Doctor Communication
Presented by La’Shardae Scott, DSW candidate, MSW, CHES, CHW, CEO/President, Scott Center for Observation Treatment and Transition
Click here to register
+myBinderRelated Content
-
Hydroxyurea (hydroxycarbamide) for sickle cell diseaseBACKGROUND: Sickle cell disease (SCD) i...
-
David Williams, MDDr. Williams is the president of Dana-Fa...
-
Howard University Hospital Center for Sickle Cell DiseaseTransitioning from pediatric to adult pr...
-
Santosh L. Saraf, MDDr. Santosh Saraf is an assistant profes...
-
Sexual Experiences in Men With Sickle Cell Disease – A Phenomenological EnquiryHuman sexuality is an integral part of o...
-
Patient Perspective: Uncompassionate Care and Suspicionhttps://www.youtube.com/watch?v=HV_5019J...
-
Brigham and Women’s Sickle Cell Disease ClinicEach person with sickle cell disease is ...
To improve your experience on this site, we use cookies. This includes cookies essential for the basic functioning of our website, cookies for analytics purposes, and cookies enabling us to personalize site content. By clicking on 'Accept' or any content on this site, you agree that cookies can be placed. You may adjust your browser's cookie settings to suit your preferences. More Information
The cookie settings on this website are set to "allow cookies" to give you the best browsing experience possible. If you continue to use this website without changing your cookie settings or you click "Accept" below then you are consenting to this.
Powered by
Support for this site is provided by
This platform is made possible through a partnership with the Sickle Cell Disease Association of America, Inc. (SCDAA) and its member organizations. SCDAA's mission is to advocate for people affected by sickle cell conditions and empower community-based organizations to maximize quality of life and raise public consciousness while advancing the search for a universal cure.