Google
Trusted Resources: News & Events
Latest announcements and gatherings
$100,000 Grant Allows National Expansion in Expert Care of Sickle Cell Patients
Researchers at the University of Tennessee Health Science Center (UTHSC) College of Nursing and St. Jude Children’s Research Hospital have received a $100,000 grant to expand an innovative education program for nurses who care for people with sickle cell disease (SCD) – an inherited illness that affects 100,000 people nationwide.
The grant from Global Blood Therapeutics, Inc. (GBT) allows the researchers to increase the impact of the Sickle Cell Boot Camp to Promote Nursing Excellence that was held in June at UTHSC. Funded through an initial $50,000 grant from GBT, the first boot camp brought 15 nurses to the UTHSC campus to learn best practices to treat sickle cell patients. The expanded program will incorporate a train-the-trainer model allowing for expansion of the program.
The nursing education program is a collaboration between the UTHSC College of Nursing, St. Jude, and the International Association of Sickle Cell Nurses and Professional Associates (IASCNAPA).
+myBinderRelated Content
-
People With Sickle Cell Are Seen as Hypochondriacs or Drug Addicts. Even a Nine-Year-Old Has to Scream to Get the Ca...Nine year old Jacob has sickle cell dise...
-
The Rise and Fall of My Mental Health With Sickle CellWe all know that mental health and ment...
-
Alloimmunization in sickle cell disease: changing antibody specificities and association with chronic pain and decre...BACKGROUND: Alloimmunization remains a ...
-
Dr. Nina AndersonDr. Nina Anderson, completed her doctora...
-
Moderate-intensity endurance-exercise training in patients with sickle-cell disease without severe chronic complicat...Background: Exercise could be a trigger...
-
Tonya M. Palermo, PhDDr. Tonya Palermo is a professor of anes...
-
Sickle Cell Anemia & Thalassaemia: An International Biomedical-Sociocultural Conference 2018The Faculty of Dentistry, Medicine and P...
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.