DISCLAIMERThe 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
email sent successfully
Trusted Resources: News & Events
Latest announcements and gatherings
Sickle Cell Summer Enrichment Camp: Piedmont Health Services and Sickle Cell Agency
Piedmont Health Services and Sickle Cell Agency will sponsor its 38th Annual Sickle Cell Summer Enrichment Camp at Camp Carefree in Stokesdale, North Carolina. Our camp will be held Sunday, July 31st through Friday, August 5th.
We are excited to open camp after missing 2 years of fun due to the pandemic! To keep our campers and staff safe, we will operate a little differently. We will take a limited number of campers this year. Campers must be 6 – 16 years of age, be North Carolina residents, and have sickle cell disease. If you are interested in your child attending, please download and complete the application and return by June 1, 2022, to secure your child’s spot. Applications will not be accepted after June 1, 2022.
Application Deadline: June 1, 2022
Camp Date: July 31 – August 5, 2022
This event has ended.
Community CenterDarryl Watkins Stays Positive in Spite of Sickle Cell DiseaseDarryl Watkins has the HbSS variant of s...
education & researchAssociation among sickle cell trait, fitness, and cardiovascular risk factors in CARDIAThe contribution of sickle cell trait (S...
news & eventsTy Montgomery says he’s not worried about sickle cell traitThe symptoms that kept Ty Montgomery out...
people & placesKaren Proudford, PhDDr. Karen Proudford is President of the ...
Community CenterWhy You Don’t Hear Much About Sickle Cell AnymoreAbout 100,000 Americans have sickle cell...
news & eventsSickle Cell Treatment ‘Life-Changing’ for Brockton BrothersEmmanuel “Manny” Johnson, 21, of Bro...
people & placesWanda BordersWanda Borders is a licensed Social Worke...
send a message
Don’t forget to join the oneSCDvoice community!
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.