We are part of the CSL Limited group of companies. See how we're Driven by Our Promise.
We collaborate with rare disease organizations to promote quality medical care and services.
We offer a variety of support programs and activities for the patients we serve.
We also aim to make sure that nothing holds you back from getting the therapies you need.
Our product portfolio focuses on innovation in new products, improved products and manufacturing expertise.
A clinical trial is a research study that is done to find out if medical treatments can improve people’s health.
We work every day as if someone’s life depends on it, because it does.
We manufacture products to treat a number of rare diseases.
Help us deliver on our promise to save lives and protect the health of people.
Diversity and inclusion are top priorities for CSL Behring.
Communications about COVID-19 go out to those living with hemophilia, von Willebrand disease.
Student, swimmer and Hemophilia B patient says his rare disease won’t hold him back.
New global data reveals the bleeding disorder is more prevalent than previously thought, according to the World Federation of…
Emmy-winning actress and Rangers coach headline National Hemophilia Foundation gala.
How John Vieke’s daughter helped him see his rare disease in a new light.
New York Rangers Head Coach and hemophilia patient David Quinn completes first season.
See one patient's tips for teens beginning to manage their rare disease.
A team representing the National Hemophilia Foundation hits the pavement.
As he prepares to head off to college, Michael Joshua is dreaming big and isn't letting hemophilia hold him back.
See hemophilia patient Michael Joshua’s tips for choosing the right school
This original animation explains.
Five ways to help your child succeed.
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