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
7th Annual Leadership Summit and General Assembly of Patients, Caregivers & CBOs
The Sickle Cell Community Consortium (SC3) is pleased to announce the 7th Annual Leadership Summit and General Assembly of Patients, Caregivers, and Community-Based Organizations (CBOs) to be held March 23-27, 2023, in Atlanta, GA. We are excited to announce that we will be in-person at the beautiful Hilton Garden Inn Buckhead this year.
We will convene the 7th annual gathering of sickle cell advocates and opinion leaders. This year’s theme, Expert Advocacy in the Digital World, is designed to provide workshops and training featuring nonprofit digital transformation, expanding the advocacy social footprint, virtual fundraising, and online activism.


Related Content
-
videos & visualsLia – A 2014 Short Filmhttps://www.youtube.com/watch?v=TcX_v6Os...
-
news & eventsSickle Cell Anemia & Thalassaemia: An International Biomedical-Sociocultural Conference 2018The Faculty of Dentistry, Medicine and P...
-
news & events2016 Annual Sickle Cell Disease Clinical Research MeetingsThe NHLBI Annual Sickle Cell Disease Cli...
-
news & eventsRare Disease Day Symposium at the Quinnipiac Frank H. Netter MD School of MedicineSince 2015, the Frank H. Netter MD Schoo...
-
news & eventsNational Abstract Competition for SCDAA’s 50th Annual ConventionIf you are a researcher, community-based...
-
news & eventsRare Disease Day at NIH 2023Rare Disease Day® takes place worldwide...
-
education & researchParents’ StoriesFor couples of African, Caribbean, Middl...
send a message
Don’t forget to join the oneSCDvoice community!
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.