CSL Behring News Hub
Vita: Sharing Stories of Biotech's Promise
HAEi emergency card in English

A Wallet-Sized Way to Ensure the Right Care

HAE International’s emergency cards help physicians provide the right care in critica…

10 Dec 2019 HAE
CSL Behring patient advocate Pete Dyson with son

Video: Raising Kids and Managing a Rare Disease

Our patients share what it’s like to be a parent living with a rare condition.

10 Oct 2019 Children
CSL Behring construction project in Marburg, Germany

Growing in Germany to Meet Demand

Biotech CSL Behring unveils expansion plans in Marburg.

12 Sep 2019 Communities
timeline of C1-INH therapy

Forty Years of Knowing How

Replacing C1-INH plasma protein gives a rare disease a longed-for treatment.

10 Sep 2019 Science
Parent, child talk with teacher

Video: How to Tell Teachers About a Rare Disease

One mom's tips for ensuring a child's condition is managed in the classroom.

23 Aug 2019 HAE
Traveling with medication photo

Video: How to Bring Medication on Vacation

We asked patients for advice on managing their rare disease while traveling.

09 Aug 2019 Lifestyle
CSL Behring Patient Advocate Lori Haigler

Video: Why My Rare Disease Doesn't Define Me

Patients on why having a rare condition is only part of their lives.

17 Jul 2019 Lifestyle
Camino de Santiago de Compostela in Spain

Turning an HAE Walk Into a Pilgrimage

Following the “Camino” in Spain, walkers will raise awareness about hereditary angioe…

15 May 2019 Wellness
Natalie Metzger, director of hereditary angioedema documentary "Special Blood"

Revisiting HAE Documentary ‘Special Blood’

Director and HAE patient Natalie Metzger on putting faces to the rare disease.

08 May 2019 Wellness
Rare disease patients talking at CSL rare disease patient summit

Bringing Rare Disease Patients Together

Patient advocates share stories to empower others living with similar conditions.

05 Apr 2019 Wellness
Rare disease doctor's stethoscope resting on top of a guitar

Is Music Therapy a Prescription for Rare Diseases?

For some patients, rhythm and beats can complement hospitals and medication.

18 Mar 2019 Wellness
Hereditary angioedema patient Machelle Pecoraro playing cards with her children.

VIDEO: What Kids Need to Know

See Machelle’s Promising Tips for helping a child be their own rare disease advocate.

08 Feb 2019 Wellness