Google
Trusted Resources: News & Events
Latest announcements and gatherings
Community Congress Ad Hoc COVID-19 Response Working Group Webinar
Community Congress Ad Hoc COVID-19 Response Working Group Webinar
Tuesday April 7 at 4:00pm EST
This webinar will be hosted by teleconference ONLY, not in-person.
Use Webex Link to view slides
or dial 1-650-479-3208
Access Code 665 002 154
Password (if prompted) 1234
This event has ended.
+myBinderRelated Content
-
FDA advises patients on use of non-steroidal anti-inflammatory drugs (NSAIDS) for COVID-19[3/19/2020] FDA is aware of news reports...
-
You Should Get a COVID-19 Vaccine – Arabichttps://www.youtube.com/watch?v=YQBfcUyB...
-
You Should Get a COVID-19 Vaccine – Mandarinhttps://www.youtube.com/watch?v=6yPsDqxi...
-
Coronavirus/COVID-19 & Sickle Cell Disorder (Sickle Cell Foundation Nigeria)What is Coronavirus? -It is a new virus...
-
COVID-19: Highest Risk Patients are Asked to Stay at Home for 12 Weeks [England]A million and a half people in England w...
-
Depression & the Sickle Cell Warrior – WebinarThe Sickle Cell Mental Health Initiative...
-
Supermarkets Offer Special Hours for Older ShoppersSome grocery store chains across the U.S...
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.
Powered by
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.