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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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news & eventsEffort set to help sickle cell patients manage medsVanderbilt University Medical Center is ...
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news & eventsThe Sickle Cell Association of New Jersey’s 10th Annual Statewide Sickle Cell Disease SymposiumOur goal is to improve and expand patien...
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news & eventsZebra Subway Car Runs Through Boston to Draw Attention to Rare DiseasesBostonians may be seeing stripes this mo...
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news & eventsAsk Me Anything Blood Donor Educational WebinarJoin us for our next 1-hour virtual educ...
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people & placesSickle Cell Thalassemia Patients NetworkSince April of 1992, the Sickle Cell Tha...
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people & placesNaomi MooreNaomi Moore is a sickle cell educator at...
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news & events2019 Cure Sickle Cell Initiative Annual Forum: Accelerating Scientific PrioritiesTuesday, November 19 - Thursday, Novembe...
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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.