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
SCDF: BabySteps Parent Education Meeting
BabySteps is a FREE monthly program for parents & families of children ages birth – 5 with sickle cell disease. Enjoy The Opportunity to: Connect with other caregivers of young children with SCD, Share & hear from others’ experiences, Discover Management tools/skills, and Expand SCD Education.


Related Content
-
people & placesCure Sickle Cell FoundationCure Sickle Cell Foundation, Inc. is a 5...
-
Community CenterAfrica Sickle Cell Watch – ASCWOur core objectives are raising awarenes...
-
news & eventsWorld Sickle Cell Awareness DaySince 2008, World Sickle Cell Awareness ...
-
people & placesNetwork of Rare Blood Disorder OrganizationsThe Network of Rare Blood Disorder Organ...
-
education & researchSickle cell disease and educationIt is often observed that sickle cell di...
-
news & eventsAnnual Sickle Cell Day Event by Sickle Cell Foundation of Georgia (SCFG)Join us for Sickle Cell Day at the Georg...
-
news & eventsPfizer’s Kevin Williams to Pen Health Column on Sickle Cell Disease for the Black PressDr. Kevin Williams, the Chief Medical Of...
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.