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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
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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.
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people & placesKathy Norcott, MSKathy Norcott, MS serves an Executive Di...
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education & researchSelf‐Management Recommendations for Sickle Cell Disease: A Content Analysis of WebsitesThis paper reports on the findings of a ...
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people & placesIII & Long FoundationThe III & Long Foundation was founde...
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videos & visualsSickle Cell Stories: Office of Minority Health, U.S. Department of Health and Human Serviceshttps://www.youtube.com/watch?v=HFojyaji...
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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.