Learning from your experiences
Thank you to all those who completed our recent Sight Loss Survey β almost 700 of you took the time to share your experiences.
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Thank you to all those who completed our recent Sight Loss Survey β almost 700 of you took the time to share your experiences.
High quality information on genetic testing and counselling for families affected by inherited sight loss is now available in one place thanks to the launch of an innovative new website, Unlock Genetics.
James Birtley is a Retina UK supporter and volunteer who is living with retinitis pigmentosa. He is also a scientist with a particular interest in the structure of proteins, the complex molecules that form the building blocks of our bodies.
Despite the knock-on effects of the pandemic, thereβs been a lot going on this year in the world of research! Here are snapshots of a few stories that have appeared in the Research News section of our website in 2022.
The Retina UK community is sometimes targeted by adverts online or in social media, offering invasive treatments for inherited sight loss.
The cover of this edition celebrates the success of our amazing London Marathon team. Together they have raised more than Β£43,000.
Information for healthcare professionals: Genetic testing and counselling in inherited retinal disease
This edition includes exciting news about our Annual and Professionalsβ Conferences. We hope as many of you as possible can join us in Manchester, or online, in September. Youβll also find updates about the latest research and a feature on one of our funded researchers, Dr JΓΆrn Lakowski.
X-linked inheritance means that the faulty gene is located on the X chromosome, the larger of the two sex chromosomes.
Inherited retinal dystrophies (IRDs) are the leading cause of blindness in working-age people in the UK, and children as young as eighteen-months are regularly diagnosed.