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
COVID-19 Health Alert for People With Sickle Cell Disease and Their Caregivers (Adapted for Sub-Saharan Africa)
April 1, 2020 – COVID-19, the coronavirus disease of 2019 – also known as Coronavirus-2 (also called SARS-CoV-2) – and the illness it causes is on everybody’s mind. If you or your family member has sickle cell disease (SCD), you may be worried about what this new disease may mean to you.
The more you learn about COVID-19, the better you can understand what to look for, how to protect yourself or your loved one, and what to do IF you feel sick. Sickle Cell Disease Association of America (SCDAA) and its Medical and Research Advisory Committee want to help you understand COVID-19, how it may affect a person with SCD, and what you can do to help. This version is adapted for sub-Saharan Africa.
The potential health risk posed by COVID-19 for people with SCD is a real concern. The knowledge we have about how COVID-19 will affect those living with SCD is evolving constantly. Information about COVID-19 may change in the coming days, weeks and months. It is important that you stay regularly informed.


Related Content
-
education & researchFDA advises patients on use of non-steroidal anti-inflammatory drugs (NSAIDS) for COVID-19[3/19/2020] FDA is aware of news reports...
-
education & researchCOVID-19 and African AmericansMuch has been published in leading medic...
-
news & eventsSickle Cell Meetup on Facebook Live and Zoom – Sickle Cell 101Sickle Cell 101 is hosting an online mee...
-
news & eventsMARAC Advisory Statement Regarding SCD Patients during the time of “Reopening” the U.S. EconomyMay 14, 2020—On Thursday April 16, 202...
-
videos & visualsSCDAA Facebook Live: Coronavirus and Sickle Cell Diseasehttps://www.facebook.com/watch/live/?v=2...
-
news & eventsWhy I Will Be Getting the COVID-19 VaccineOn Nov. 9, Pfizer and BioNTech announced...
-
news & eventsGBT Supports Sickle Cell Patients During COVID-19 PandemicGlobal Blood Therapeutics (GBT) is takin...
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.