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
-
Management of Sickle Cell Disease SymposiumThe Management of Sickle Cell Symposium ...
-
Stepping Up: Calvanay’s advicehttps://www.youtube.com/watch?v=_x9Dhrim...
-
Promising results at 1 year follow-up following familial haploidentical (FHI) T-cell depleted (TCD) with CD34 enrich...AlloSCT from HLA-matched MSD has been su...
-
University of North Carolina at Chapel Hill School of Medicine, Division of Hematology/OncologyThe Division of Hematology/Oncology offe...
-
Disability evaluation under social security (hematological disorders – childhood)A. What hematological disorders do we ev...
-
Kenneth R. Peterson, PhDKenneth R. Peterson is the Professor and...
-
Coronavirus Preparedness for People With Chronic Diseaseshttps://www.youtube.com/watch?v=G_JC3vUT...
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.