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
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
Columbus, OH
This event has ended.
Related Content
-
videos & visualsSickle Cell Disease: Taking Charge of Your Health Part 1 – Real-World Patient Perspectiveshttps://www.facebook.com/watch/?v=343267...
-
videos & visualsInfographic: Understanding Sickle Cell Disease – ASHhttps://www.onescdvoice.com/wp-content/u...
-
news & eventsSCD Clinical Trials Network Workshop – New York, NYJoin us for an afternoon of fun acti...
-
videos & visualsSickle Cell Disease Coalition (SCDC)https://www.youtube.com/watch?v=oQP-Uq0B...
-
people & placesMaidunama Sickle Cell FoundationMaidunama Sickle Cell Foundation is prin...
-
news & eventsProclamation on National Sickle Cell Disease Awareness Month, 2020 – By the President of the United States of ...As our nation recognizes National Sickle...
-
news & eventsNational Sickle Cell Advocacy Day 2020 — Sickle Cell Disease Association of America – CANCELEDPlease join the Sickle Cell Disease Asso...
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.