Google
Trusted Resources: News & Events
Latest announcements and gatherings
Let Your Light Shine: Sickle Social
Piedmont Health Services and Sickle Cell Agency & Bridges Pointe, Inc. present night of fun and awareness.
Join us for the Sickle Social: Meet and greet, patient panel, & get a chance to hear from Sickle Cell experts about the future of Sickle Cell. Be sure to wear your red shirts and red face mask!
Date & Time:
Friday, June 19, 2020
Meet and greet: 5:45 PM
Sickle social: 6:00 PM to 7:00 PM
This event has ended.
+myBinderRelated Content
-
RARE Patient Advocacy SummitEach year, Global Genes convenes one of ...
-
Sickle Cell Disease: a battle for equality, justice and respect | Ahmar Zaidi | TEDxDetroithttps://www.youtube.com/watch?v=RAvi5y95...
-
Today’s Faces of Sickle Cell Disease: Marqus ValentineWhen Marqus Valentine went to junior col...
-
Michelle’s House (Sickle Cell Disease Association of America Southern CT)At Michelle's House, home of the Sickle ...
-
2020 RARE on the Road – RaleighThe EveryLife Foundation for Rare Diseas...
-
Machnik Sickle Cell Foundation UgandaMachnik Sickle Cell Foundation Uganda (M...
-
Andrea M. WilliamsAndrea Williams founded and leads the Ch...
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.