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
National Sickle Cell Advocacy Day 2020 — Sickle Cell Disease Association of America – CANCELED
Please join the Sickle Cell Disease Association of America as we advocate for those affected by sickle cell disease. On Advocacy Day, we focus on key legislative issues that are important to individuals living with SCD and their families, including promoting stable funding for research, better healthcare access, expanded programs, and increased education and awareness for the SCD community and programs throughout our nation.
The Advocacy Day is postponed until Spring 2021 due to the coronavirus.
Please stay tuned for further updates.
Related Content
-
Community CenterSickle Cell 101Sickle Cell 101 is a 501(c)(3) nonprofit...
-
people & placesNancy M. ReneNancy is the grandmother of a child with...
-
people & placesSantonio HolmesSantonio Holmes recognized the great nee...
-
people & placesThe Sickle Cell Cares FoundationThe Sickle Cell Cares Foundation was est...
-
people & placesNortheast Louisiana Sickle Cell Anemia FoundationThe Northeast Louisiana Sickle Cell Anem...
-
news & eventsKNOWvember Webinar: A grandparent’s voice – Advocacy and support for chronic pain familiesWhile parents are often the prim...
-
videos & visualsNew Book Tackles Being a Kid With Sickle Cell Diseasehttps://www.youtube.com/watch?v=sY1iDlKR...
send a message
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.