DISCLAIMERThe 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
email sent successfully
Trusted Resources: News & Events
Latest announcements and gatherings
Rare Disease Day at Nationwide Children’s
Rare Disease Day at Nationwide Children’s is a part of a global observance, join us to raise awareness about rare diseases and their impact on patients and families.
This event is free and open to the public, including patients, their families and caregivers, healthcare providers, and research professionals.
Date & Location:
February 28, 2023
4:30 PM – 8:00 PM
Nationwide Children’s Hospital Education Center
This event has ended.
people & placesSickle Cell Warriors of WisconsinSickle Cell Warriors of Wisconsin is a v...
people & placesJohn James, OBEJohn James is the chief executive of the...
education & researchMedicaid and CHIP Sickle Cell Disease Report, T-MSIS Analytic Files (TAF) 2017Sickle cell disease (SCD), the most prev...
videos & visualsSickle Cell Disease Managing Painhttps://www.onescdvoice.com/wp-content/u...
people & placesAllan F. Platt, MMSc, PA-C, DFAAPAAllan Platt has served as co-founder and...
people & placesSickle Cell Foundation of Palm Beach CountySickle Cell Foundation of Palm Beach Cou...
news & eventsPresidential Message on National Sickle Cell Disease Awareness Month 2019National Sickle Cell Disease Awareness M...
send a message
Don’t forget to join the oneSCDvoice community!
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.