Find support and community through others living with acquired/immune-mediated thrombotic thrombocytopenic purpura (aTTP/iTTP*)

There are a number of organizations dedicated to providing information and support to people living with aTTP/iTTP and rare diseases.

Answering TTP Foundation >

National Organization for Rare Disorders (NORD) >

The Platelet Disorder Support Association >

Global Genes >

Patient, Heather, facing camera and smiling

Heather, real patient. Individual results may vary.
Heather is being compensated by Sanofi.

Note that the opinions expressed by the organizations above do not necessarily reflect the views of Sanofi. Sanofi does not maintain and is not responsible for the content of communications for the listed organizations or their websites. This is not intended to be a comprehensive list of aTTP/iTTP disease support organizations and additional resources may be available and should be investigated. These listings do not constitute an endorsement by Sanofi of information provided by any other organizations.

CABLIVI Patient Solutions is available to support you and your loved ones throughout an aTTP/iTTP episode

If you’re in the hospital with aTTP/iTTP, heading home with CABLIVI, or wondering what kind of support is out there in case of another aTTP/iTTP episode, know CABLIVI Patient Solutions is here to help.

Learn more >


Enroll today >

Resources are available about CABLIVI, including how to take it at home and what to discuss with doctors

Videos about CABLIVI—from people’s stories to how to take therapy at home—are available to you


*aTTP is also known as iTTP. You and your healthcare team can use either term.
aTTP/iTTP=acquired/immune-mediated thrombotic thrombocytopenic purpura;TTP=thrombotic thrombocytopenic purpura.