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.
Watch Online: Swimming With the Dolphins
Find out how animal therapy works and why children who have Hemophilia B went for a swim with these friendly mammals in the F…
5 Things To Know About Hemophilia B
Hemophilia B patients are missing clotting Factor IX but treatments have come a long way - with more innovation in progress.
Watch online: "Medical Stories" of Hemophilia B
The series, being aired on PBS, shares personal journeys and the scientific quest for treatments.
Coming to PBS: Telling the Story of Hemophilia B
New series “Medical Stories,” is headed for public television stations in the United States.
Bleeding Disorder Patient Groups Respond
Communications about COVID-19 go out to those living with hemophilia, von Willebrand disease.
Meet Michael Joshua
Student, swimmer and Hemophilia B patient says his rare disease won’t hold him back.
Getting a Handle on Hemophilia
New global data reveals the bleeding disorder is more prevalent than previously thought, according to the World Federation of…
Star Power at the Red Tie Soiree
Emmy-winning actress and Rangers coach headline National Hemophilia Foundation gala.
Video: A Father’s Bond
How John Vieke’s daughter helped him see his rare disease in a new light.
Rare Ranger
New York Rangers Head Coach and hemophilia patient David Quinn completes first season.
Watch: How Teens Can Take Charge
See one patient's tips for teens beginning to manage their rare disease.
Running the NYC Half Marathon
A team representing the National Hemophilia Foundation hits the pavement.
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