Sickle Cell Disease
What Is It Like to Have Sickle Cell Disease?
In their own words, patients and caregivers describe the disease’s emotional toll.
Marking Sickle Cell Disease Awareness Month
U.S. recognizes important need for research into inherited blood condition.
Family Unites Against Sickle Cell Disease
Instead of the usual reunion, 50+ family members rolled up their sleeves to help those who have sickle cell disease.
An All-Too Common Rare Disease
Sickle cell disease patients have been waiting a long time for a breakthrough; CSL Behring’s expert on what’s next for those …
Sickle Cell Disease Caregivers' Guide
Caregivers play a multifaceted role. Here’s how to support a loved one who has this inherited blood disorder.
Santonio Holmes Tackles Sickle Cell Disease
The Steeler legend - and Dad to a son with the disease - visits our podcast to talk about his foundation that helps families …
COVID-19 and Sickle Cell Disease
Experts, including CSL Behring’s Dr. Greg Kato, weigh whether sickle cell patients are more at risk of severe impacts from co…
Patients as Partners
Healthcare panel will explore how tech can build a bridge and involve patients every step of the way.
Advice for Young Sickle Cell Patients
Learn how young adult sickle cell disease patients can move out of pediatric care and take control of their health.