Google
Trusted Resources: News & Events
Latest announcements and gatherings
Sickle Cell & Me: Survivor Discussion with Clarisse H. (Sickle Cell Survivor)
The Lambda Epsilon Sigma Chapter of Sigma Gamma Rho Sorority Inc. (SGRho) is partnering with Clarisse H. to share her journey battling sickle cell anemia. Learn how she manages motherhood with sickle cell.
Sickle Cell & Me: Survivor Discussion with Clarisse H. (Sickle Cell Survivor)
Sunday, May 21, 2023
5:00 pm–6:00 pm EDT
via Zoom
+myBinderRelated Content
-
Today’s Faces of Sickle Cell Disease: Deidra Flowers-WilliamsAt six months of age, Deidra Flowers-Wil...
-
Charlotte 13-Year-Old With Sickle Cell Plays Lead Role in Broadway’s ‘Lion King’"The Lion King" opens Wednesday night at...
-
When Cracking Down On Opioids Means Tougher Access For Sickle Cell PatientsMany people with sickle cell disease wil...
-
Sick CellsSick Cells' mission is to elevate the vo...
-
Gene Therapy: What You Need to Know (Warrior FAQs)Two gene therapies were recently approve...
-
Reasonable Accomodations for College Students With Sickle Cell DiseaseSome of the rules at college make it har...
-
Patient Perspective: Uncompassionate Care and Suspicionhttps://www.youtube.com/watch?v=HV_5019J...
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.