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.
Planning a Virtual Rare Disease Day
Rare disease advocates will log on this year to keep the cause front and center.
Show Your Stripes, Zebras!
Rare disease patients have adopted the zebra as an icon. Find out why.
A Spotlight on CIDP
Learn more about this rare neurological disorder.
Finding Purpose-Driven Work
Serving patients and working to protect public health weaves meaning into all roles at CSL, says our Chief Human Resources Of…
Watch: Why Rare Disease Day Matters to Us
Patients are “core to our DNA” so take time out to recognize them and their communities, says our Chief Medical Officer.
Meet Michael Joshua
Student, swimmer and Hemophilia B patient says his rare disease won’t hold him back.
Listen: Chasing the Cure
Doctor’s book tells story of researching his own rare disease.
To Turn Inward or Reach Out?
Alpha 1 patient – and advocate for others – Richard Lovrich shares his philosophy about coping with a rare disease.
Parents, Kids and Rare Disease
When a rare disease is part of family life, expect a few extra challenges.
Video: On Patience and Hard-to-Diagnose Illnesses
Lynne Doebber, who was ill for decades before her diagnosis, offers advice to those still searching for answers.
Audrey Hepburn - an Icon for Rare Disease Advocacy
EURORDIS-Rare Diseases Europe bestows posthumous honor on the actress and humanitarian; Hepburn’s son is an advocate for rare…
Get Some Animated Advice
Our hero patient takes on issues like being undiagnosed, how to talk to the doctor and getting support from friends.
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