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
Pfizer and National Newspaper Publishers to Raise Awareness About Sickle Cell Disease
Pfizer and the National Newspaper Publishers Association (NNPA) are collaborating to increase awareness about sickle cell disease and to discuss the need for improved patient care, as well as the importance of clinical trials.
The National Heart, Lung and Blood Institute (NHLBI) of the National Institutes of Health (NIH) estimates that sickle cell disease currently affects up to 100,000 Americans, making it the most common inherited blood disorder in the U.S.
The disease affects many ethnic groups, but people of African descent seem to be hit the hardest by the blood disorder, say researchers at the American Society of Hematology. The Centers for Disease Control and Prevention (CDC) statistics show that sickle cell disease occurs in approximately one out of every 365 African-American births.
Related Content
-
Community CenterSickle International Family CoalitionThe mission of the Sickle International ...
-
people & placesTosin Ola-Weissmann, RNTosin Ola, BSN, RN (aka Sickle Cell Warr...
-
people & placesThe Sickle Cell Foundation, Inc. – Central Alabama ChapterThe Sickle Cell Foundation, Inc. - Centr...
-
Community CenterSickle Cell Society IrelandSickle Cell Society Ireland (SCSI) is th...
-
Community CenterLiving Well With Sickle Cell: Andre Harris (Video)My name is Andre Harris. We are in Houst...
-
people & placesKaren Proudford, PhDDr. Karen Proudford is President of the ...
-
news & eventsHemoglobinopathy Counselor Training Course – VIRTUALUPDATE! 2020 Hemoglobinopathy Counselor ...
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.