| 09 February 2017

Rare Diseases International Policy Event

http://www.retina-international.org/

‘No country can claim to have achieved universal healthcare if it has not adequately and equitably met the needs of those with rare diseases’

Helen Clark, Administrator of the UN Development Programme


| 26 January 2017

We Want To Hear From You!

Retina International, with the support of member organisations, has designed the following survey to gather information on the real life experience of Patients affected by Inherited Retinal Disease (IRDs) in accessing Genetic Testing services in their countries of residence. This will aid us in developing appropriate communication and educational materials for our community globally. 

For further information email info@retina-international.org 

Click below to access the survey. 

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