Ambassadors
Here at Retina UK we have some truly amazing volunteer Ambassadors, who help to spread the word about our important work and share their inspirational stories.
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Here at Retina UK we have some truly amazing volunteer Ambassadors, who help to spread the word about our important work and share their inspirational stories.
Steve is a Paralympian who was diagnosed with retinitis pigmentosa (RP) in 2011.
Her work with us enables her to achieve her aim of empowering others living with similar conditions to her own.
A research project funded by Retina UK helped pave the way to a new gene therapy that has recently produced encouraging results in two young people with achromatopsia, a condition that causes complete colour-blindness and poor overall vision from birth.
The latest research news piece from Retina UK.
Our volunteers are highly valued members of the Retina UK team and their roles are essential to help support and enable people affected by inherited sight loss to live fulfilling lives.
X-linked inheritance means that the faulty gene is located on the X chromosome, the larger of the two sex chromosomes.
Beacon Therapeutics announced positive results from their phase 2 gene therapy trial for X-linked retinitis pigmentosa (XLRP) caused by mutations in the RPGR gene.
It was previously believed that female carriers of X-linked inherited retinal diseases (IRDs) like X-linked retinitis pigmentosa (RP and Choroideremia) remained unaffected by sight loss.
UK researchers have discovered that passing a weak electrical current between electrodes on a person’s scalp may lead to a reduction in frequency of the visual hallucinations experienced by some people living with sight loss.