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
2021 WEPSCF Rockin’ the Red – 16th Annual Event
Join us for a Zoom gathering as we celebrate National Sickle Cell Awareness Month.
We look forward to seeing you ONLINE and IN RED!
Date & Time:
September 28, 2021
06:00 PM – 07:00 PM
This event has ended.
+myBinderRelated Content
-
videos & visualsAttorney Terri Booker talks about life with Sickle Cell on World Sickle Cell Awareness Dayhttps://www.fox29.com/video/576000...
-
people & placesLeigh Ann Wilson, LCSWLeigh Ann Wilson is a licensed clinical ...
-
people & placesSickle Cell Thalassemia Patients NetworkSince April of 1992, the Sickle Cell Tha...
-
Community CenterSickle Cell Disease isn’t Laughable, But It Has a Comedic Ambassador — Kier “Junior” SpatesMr. Spates believes in living a full lif...
-
people & placesKyle A. SmithKyle Smith is a sickle cell warrior and ...
-
news & eventsRare Diseases and Orphan Products Breakthrough SummitEach year, the NORD Summit, one of the l...
-
news & eventsGreenville program tries team approach to improve lifespan of sickle cell disease patientsDr. Alan Anderson who was involved with ...
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.