Podcast: All about Retina UK!
We sat down to discuss all about who Retina UK are.
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We sat down to discuss all about who Retina UK are.
We sat down to discuss what our volunteers got up to on Retina UK day.
With the General Election fast approaching we thought we would take a deep dive into accessible voting with Special Projects Lead, Matthew Carr.
With a significant proportion of inherited retinal conditions being caused by unidentified genetic faults, and many families unable to get clear results from genetic tests in clinic, the project set out to solve previously undiagnosable cases and discover more of the genes and mutations that are associated with sight loss.
A chat with our founder, Lynda Cantor MBE and our (former) Head of Fundraising, Deborah Laing.
Whether you are looking for practical information or emotional support, online, by phone or face-to-face, we’re here to help.
There are many ongoing clinical and laboratory studies around the world, exploring innovative approaches to treating inherited sight loss.
The aim of the site is to increase the level of awareness and understanding of genetic testing and genetic counselling among people living with inherited retinal dystrophies, empowering them to make fully informed decisions about their lives, healthcare and family planning.
Our monthly e-Newsletter featuring the latest updates from Retina UK. Subscribe now to receive these updates directly to your email.
Our monthly e-Newsletter featuring the latest updates from Retina UK. Subscribe now to receive these updates directly to your email.