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.
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.
CSL Behring will sponsor free training in artificial intelligence for high school students in Philadelphia and Los Angeles.
The National Hemophilia Foundation honored 58 U.S. teens for speaking up, taking action and leading by example.
Patients offer advice for graduating high school students about managing a health condition in a university environment.
Hereditary angioedema, a challenging rare disease to manage, causes serious swelling episodes. Children can have them, too.
For students who manage a chronic condition, COVID-19 isn’t the only back-to-school concern. Get three tips for staying healt…
Right now, there are more questions than answers. Three experts offer advice on coping with unknowns.
Young rare disease patient – and nonprofit founder – continues to grow her mission to bring furry comfort to those who need i…
Let this video – taken at our annual event for kids with bleeding disorders – answer the question.
More than 100 kids and teens participated in CSL Behring’s national sports competition for athletes who have bleeding disorde…
Our patients share what it’s like to be a parent living with a rare condition.
“Hope Lives Here” connects Jamaican teens living with blood disorder.
Mentors can help guide young sickle cell disease patients.
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