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
Coping With Anxiety & Fear From Quarantine Dr. Gayle Rogers – Webinar
The Sickle Cell Mental Health Initiative of the Sickle Cell Community Consortium is committed to working with the patients, caregivers, and community-based organizations (CBOs) of the sickle cell community to provide mental health support amid COVID-19.
Click the link to join this Webinar by the Sickle Cell Mental Health Initiative.
Schedule:
Tuesday, April 21, 2020 | 7 PM EST, Webinar Discussion With Q&A
Wednesday, April 22, 2020 | 7 PM EST, Community Chat
This event has ended.


Related Content
-
videos & visualsSCD/ Thalassaemia and COVID-19: Possible Risks and a Proposal for a Patient Pathway During the Pandemic – Webi...https://www.youtube.com/watch?v=ENKX7Kf6...
-
education & researchCDC Updates, Expands List of People at Risk of Severe COVID-19 IllnessOlder adults and people with underlying ...
-
news & eventsCOVID-19 Health Alert for Patients and Caregivers – SCDAAMay 27, 2020 – COVID-19, the coronav...
-
videos & visualsYou Should Get a COVID-19 Vaccine – Frenchhttps://www.youtube.com/watch?v=5DMfiyA0...
-
education & researchSickle Cell Disease and COVID-19: What We’re Telling PatientsMonths into the pandemic, we’re learni...
-
news & eventsThe Role of Caregivers in Sickle Cell Disease and the Impact of COVID-19We are excited to present our Seventh An...
-
videos & visualsYou Should Get a COVID-19 Vaccine – Spanishhttps://www.youtube.com/watch?v=awFzaU9c...
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.