DISCLAIMER
The information and materials accessed through or made available for use on any of our Sites, including, any information about diseases, conditions, treatments, or medicines, are for informational purposes only. The Content is not intended to be and is not a substitute for professional medical advice, diagnosis, or treatment, and your participation on our Sites does not create a healthcare professional-patient relationship. You should consult a doctor or other qualified health care professional regarding any questions you have about your health or before making any decisions related to your health or wellness. Call your doctor or 911 immediately if you think you may have a medical emergency.compose your message
message sent
email sent successfully
Trusted Resources: News & Events
Latest announcements and gatherings
Sickle Cell Anemia Research: Survey for Residents of Georgia
The purpose of this survey is to gather information for a study by Chloe Kim, a student at George Walton High School. The study is to determine how the racial bias in sickle cell disease affects patient experience in Georgia. The survey is anonymous, and your answers are completely confidential and will be released only as summaries in which no individual’s answers can be identified. There is no compensation for participation.


Related Content
-
education & researchBedside Lung Ultrasound During Acute Chest Syndrome in Sickle Cell DiseaseLung ultrasound (LU) is increasingly use...
-
news & eventsRoland B. Scott Memorial Symposium: I Want Somebody to LoveRoland B. Scott Symposium on Sickle Cell...
-
education & researchCognitive function, coping, and depressive symptoms in children and adolescents with sickle cell diseaseOBJECTIVE: The objective of this study ...
-
news & eventsWarrior University: Curative Therapies SeriesWarrior University is an online, curricu...
-
news & eventsLong-term opioids may not be best pain management option for all sickle cell patientsSmall study shows some on opioids report...
-
news & eventsKNOWvember Webinar: A grandparent’s voice – Advocacy and support for chronic pain familiesWhile parents are often the prim...
-
videos & visualsSickle Cell and Travel With Dr. Coretta Jenerette – EMBRACE Traveling With Sickle Cellhttps://www.youtube.com/watch?v=oz2nHyMZ...
send a message
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.
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.