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
Roland B. Scott Memorial Symposium: I Want Somebody to Love
Roland B. Scott Symposium on Sickle Cell Disease
“I Want Somebody to Love”
Friday, May 19, 2023
Live and Virtual Event, 10 am –3 pm
W. Lester Henry Auditorium
Howard University Hospital
This event will explore stigma, relationships and reproductive issues for those living with sickle cell disease. It will include two panels and a town hall, as well as awards and memorials.
Speakers include Teonna Woolford and Ahmar U. Zaidi, MD.


Related Content
-
education & researchWhat You Should Know About Sickle Cell Disease and PregnancyWhat should someone with sickle cell tra...
-
videos & visualsCoronavirus Preparedness for People With Chronic Diseaseshttps://www.youtube.com/watch?v=G_JC3vUT...
-
news & eventsThe Empowered Caregivers Forum: A Support Resource for Parents / Caregivers of Warriors With Sickle Cell / Thalassem...Join Carla Lewis, CEO of Kids Conquering...
-
news & eventsCapitol Hill Briefing Held to Encourage Sickle Cell Research and TreatmentEarlier today, a briefing was hosted on ...
-
news & eventsEx-rutgers stars Devin and Jason McCourty top $1M in fundraising for charityAbout 200 donors showed up Saturday afte...
-
education & researchMistrust of Pediatric Sickle Cell Disease Clinical Trials ResearchINTRODUCTION: Sickle cell disease (SCD) ...
-
news & events6th Annual Sickle Cell Patient and Family Educational SymposiumThe Sickle Cell Warriors Convention is a...
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.