Retina International
Retina International

Welcome to Retina International

Retina International (RI) is a patient-led, global, umbrella NGO for patient-led groups around the world focused on research and support for rare and common retinal diseases.


What We Do

For almost 40 years, Retina International (RI) has been the voice of patient-led voluntary groups, charities and foundations world wide who fund and support Retinal Research that is seeking a cure for Retinitis Pigmentosa (RP), Macular Degeneration, Ushers Syndrome & Allied Retinal Dystrophies.

Inherited Retinal Disease Toolkit

An educational resource designed for patients with IRDs, their representatives and their healthcare professionals to address the challenges of vision health and blindness.

Find out more

AMD Toolkit

An educational toolkit for a multi-stakeholder audience related to Age-related Macular Degeneration

Find out more

Sending a Red Alert!

A Toolkit on Genetic Testing Services to Inform those with Rare Eye Disease

Find out more

Diabetic Eye Disease Toolkit

 

Find out more

Patient Information

Learn more about your eyes and the many inherited, rare and genetic forms of sight loss as well as age related and common diseases of the Retina.


Learn More

Become a Member

Learn how you can become a member of our community

Learn More

Latest Updates

12.12.2019 | News

Victory for Rare Disease Patients as Rare Diseases included in UN Political Declaration on UHC
09.12.2019 | News

WHO Launches First World Report on Vision
04.12.2019 | Uncategorized

ERN-EYE Clinical Research Workshop

Join Our Mailing List

To keep up to date with our news and activities, please complete this simple form

Retina International
Ausstellungsstr. 36
8005 Zurich
Switzerland

Contact Us
+41 (0)44 444 10 77
info@retina-International.org

Follow Us
Twitter
Youtube

This site has been supported through an unrestricted educational grant from Novartis

Novartis
Font Resize
High Contrast