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
U.S. Government Awards Missouri Researcher $4.3 Million to Study Sickle Cell in Teens, Adults
The National Institutes of Health (NIH) has awarded a $4.3 million research grant to Dr. Allison A. King of the Washington University School of Medicine in St. Louis to support her research on sickle cell disease, with particular focus on teens and adults.
The grant — believed to be the first of its kind from the NIH — will let King continue and expand her study as part of an initiative being coordinated by the agency’s National Heart, Lung, and Blood Institute. The NHLBI has now awarded $36 million in sickle cell research grants to investigators at eight sites.
Related Content
-
people & placesAndrea M. WilliamsAndrea Williams founded and leads the Ch...
-
news & eventsSickle Cell & Me: Survivor Discussion with Clarisse H. (Sickle Cell Survivor)The Lambda Epsilon Sigma Chapter of Sigm...
-
Community CenterUnder The Radar: Sickle Cell DiseaseIn the U.S., an estimated 100,000 Americ...
-
people & placesSantonio HolmesSantonio Holmes recognized the great nee...
-
Community CenterToday’s Faces of Sickle Cell Disease: Mercy MendozaMercy Mendoza was born in Honduras, and ...
-
Community CenterSickle Cell Information CenterThis site is a collaboration between mem...
-
education & researchSpark Good Care GuideAs a person living with or caring for so...
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.