This website has been produced by Shire and is not intended for residents of the USA.

We use cookies to ensure that we give you the best experience on our website. By continuing to browse this site, you are agreeing to our use of cookies. Continue Find out more

Where to Learn More About Hunter Syndrome

Advocacy Groups

The International MPS Network

The International MPS Network is the official body of the patient associations representing MPS and MPS Societies at a European and global level.


Additional Resources for Rare Diseases


EURORDIS is a non-governmental patient-driven alliance of patient organizations representing more than 510 rare disease patient groups in 48 countries.


You are being redirected to, a website approved for a US audience.

You will be taken there automatically in 5 seconds. Otherwise you can click on this link right now.

MPS Day 2017

Close or ESC