Google
Trusted Resources: News & Events
Latest announcements and gatherings
Sickle Cell Disease- Let’s Talk About it Family Fun Day
Sickle Cell Partners of the Carolinas (SCPOC) invites you to join us for an afternoon of fun and engagement at “Sickle Cell Disease… Let’s Talk About It Family Fun Day” on Saturday, September 10, 2022, from 1 PM TO 5 PM at Midtown Park in Charlotte, NC. Please register for this FREE event using the QR code on the flyer or on Eventbrite at SCDLetsTalkAboutItFamilyFunDay.eventbrite.com. Patients, families, and the community at large are welcome to attend this event for FREE as we celebrate the month of September as Sickle Cell Awareness month.
During the pandemic, like many organizations, we put our in-person events on hold. Our signature day conference, ”Sickle Cell Disease… Let’s Talk About It” has been revamped to offer some of the same great topics and fun activities that many in our community have come to expect from SCPOC in an open-air park setting.
When:
Sat, September 10, 2022
1:00 PM – 5:00 PM EDT
Where:
Midtown Park
510 South Kings Drive
Charlotte, NC 28204, USA
This event has ended.
+myBinderRelated Content
-
Expert answers on kids healthWhen it comes to taking care of yourself...
-
Today’s Faces of Sickle Cell Disease: Deidra Flowers-WilliamsAt six months of age, Deidra Flowers-Wil...
-
Ify Osunkwo, MD, MPHDr. Ify Osunkwo, a specialist in hematol...
-
What it’s like to be 17 and living with sickle cell diseaseTre Adegoroye is 17 and was diagnosed wi...
-
Nancy Green, MDNancy Green, MD is a pediatric hematolog...
-
Survival in Sickle Cell Disease: Data from a Well-Resourced, National Health System SettingBackground: In well-resourced countries,...
-
Safety and early hints of benefit seen in phase 1b trial of PF-04447943Sickle cell disease (SCD) patients were ...
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.