Today is the last day of #RetinitisPigmentosaAwarenessMonth and also #RareDiseaseDay. Many people live with undiagnosed, misdiagnosed or misunderstood conditions. Today we recognise these experiences & advocate for improved healthcare, support & policies for the community.
Retina Australia retweeted
BIONIC EYE TRIAL RESULTS SHOW SUBSTANTIAL VISION IMPROVEMENTS OVER TWO AND A HALF YEARS Blind participants with retinitis pigmentosa able to locate doorways, avoid obstacles
SEGMENT
Filmed in Melbourne and Sydney | February 2025
Released on Retinitis Pigmentosa Awareness Month
INTERVIEWED
Professor James Fallon,
Chief Technology Officer, Bionics Institute @BionicsInst & Head of the Medical Bionics Department, University of Melbourne @UniMelb
Associate Professor Penelope Allen,
Head of Bionic Eye Project & Principal Investigator,
Centre for Eye Research Australia (CERA) @EyeResearchAus & Vitreoretinal Surgeon,
The Royal Victorian Eye and Ear Hospital @EyeandEarHosp
Dr Ash Attia @ash_ashattia
Chief Executive Officer & Managing Director
Bionic Vision Technologies
Results of the first clinical trial of Australia’s ‘second generation’ bionic eye have demonstrated ‘substantial improvement’ in four participants’ functional vision, daily activities and quality of life over a period of more than two and a half years.
Detailed outcomes from the trial, led by the Centre for Eye Research Australia, Bionics Institute, University of Melbourne and Royal Victorian Eye and Ear Hospital, were published in Ophthalmology Science.
The findings add to interim results which showed that the second-generation bionic eye developed by Australian company Bionic Vision Technologies provided rapid improvements for four patients with blindness caused the genetic eye condition retinitis pigmentosa.
Retinitis pigmentosa is an inherited retinal disease which affects about two million people worldwide and is one of the leading causes of vision loss in working-age people.
The bionic eye comprises an electrode array, designed by the Bionics Institute and the Centre for Eye Research Australia, that is surgically implanted behind the eye. The electrode receives signals from a video camera mounted on glasses, which stimulate the patient’s retina.
Credit: Retinitis pigmentosa fact sheet from Retina Australia @RetinaAustralia
Australian Health Journal @AUHealthJournal
Produced and published by AUDIENCED
Get your interviews captured across Australia audienced.org/contact
Meet Peter Vance, singer-songwriter living with #RetinitisPigmentosa. For #RPAwarenessMonth, he's been raising awareness through #RetinaAustralia’s Do It in The Dark campaign, spreading hope for a brighter future.! #RPawareness #RP #VisionLoss🎶✨youtube.com/watch?v=qB8tFOh0…
28th February is Rare Disease Day. @Retina_Int is hosting a webinar on 21st Feb to discuss the impact on mental health. Register at [email protected].
#rarediseaseday2025 #rarediseaseday #irds #inheritedretinaldiseases #retinaaustralia
It’s not too late to raise awareness for #RetinitisPigmentosa this February! Host a Do It in The Dark (DITD) event with #RetinaAustralia. Wear glasses simulating tunnel vision & raise funds for medical research. More info: lnkd.in/e3mEwWxb#RetinitisPi…
#RetinitisPigmentosa (#RP) is a genetic eye condition that causes progressive #visionloss. It starts with night blindness, followed by tunnel vision, and eventually can affect central vision leading to blindness.
Let’s raise awareness! retinaaustralia.com.au/help-…
#RPawareness
February is #RetinitisPigmentosa (RP) Awareness Month!
Help raise awareness & funds for RP research:
1. Register for a Do It in The Dark event
2. Share your story & raise awareness
3. Donate to research
More info: retinaaustralia.com.au/help-… #DoItInTheDark #RetinaAustralia
Today is World Geographic Atrophy (GA) Day. Join the movement to raise awareness for this progressive form of age-related macular degeneration (AMD). Find out more at: tr.ee/SumJe8IJic
#retinaaustralia #geographicatrophy #ga #worldgaday
The Summer 2024/25 edition of our bi-annual newsletter Retina Reporter is OUT NOW!
Download it here: tr.ee/_a3nIIvEJf or SUBSCRIBE here: tr.ee/k6OeQqQORI
#inheritedretinaldisease #retinaaustralia #retinitispigmentosa #geographicatrophy #generesearch #eyeresearch
Support life-changing research for people living with inherited retinal diseases by making a donation to our 2024 Christmas Appeal. Together, we CAN make a difference!
Donate today at: tr.ee/Fwv6ibXrjz
#retinaaustralia #inheritedretinaldisease #genetherapy #ChristmasAppeal
Retina Australia is delighted to announce the 2nd recipient of a $60,000 Research Grant for 2025 is Dr Jiang-Hui (Sloan) Wang from @EyeResearchAus, with his study advancing Usher Syndrome type 1B gene therapy.
tr.ee/QziF-0ICmu
#retinaaustralia #inheritedretinaldisease
We are delighted to announce the first of two 2025 Research Grant recipients, Professor Robyn Jamieson. Robyn's project aims to develop gene replacement therapies for autosomal recessive (AR) IRDs where no treatments currently exist. More info here: tr.ee/QziF-0ICmu
Representing the Steering Committee of The Inherited Retinal Disease Priority Setting Partnership, Retina Australia CEO Julia Hall and A/Prof Lauren Ayton from the University of Melbourne & CERA, at the @RANZCO Congress 2024. #inheritedretinaldisease #ranzco2024 #retinaaustralia
Spreading the word about inherited retinal disease at the @RANZCO 2024 Congress in Adelaide. Great to connect & hear about research into IRDs and the increasing understanding and importance of genetics in diagnosis & treatment
#ranzco2024 #inheritedretinaldisease #retinaaustralia
Great to be a part of Vision 2020 Australia's Parliamentary Friends Group for Eye Health and Vision Care Cocktail Function and Exhibition in Canberra - another terrific opportunity to raise awareness of IRDs. #inheritedretinaldisease #worldsightday #loveyoureyes #retinaaustralia
We are thrilled to share the Top 10 Research Priorities for Inherited Retinal Disease, from the perspective of individuals with lived experience, families, carers, and health professionals. Full report here: tr.ee/FXNiCxItbl
#inheritedretinaldisease #retinaaustralia

ALT Photo of people at launch event – from left: Associate Professor Anai Gonzalez-Cordero – Children’s Medical Research Institute (CMRI), Carly Iles – Vision 2020 Australia, Julia Hall – Retina Australia, Tim James MP, Professor Robyn Jamieson – CMRI; The Children’s Hospital; University of Sydney, Dr Eden Robertson – UNSW Medicine & Health; CMRI
Thank you @Vision2020Aus for inviting Retina Australia to its eye screening event at the Parliament of NSW. World Retina Day is this Sunday, 29th September.
@richiewilliamson and @GeoffProvest100 tried our DITD puzzle challenge. More info:
tr.ee/dECtHAvSCB
#worldretinaday
The Geographic Atrophy: We Can't Wait and See report was launched last week, and highlights the urgent need to address the impact of geographic atrophy (GA), one of the leading causes of loss of vision and blindness. Read more here: tr.ee/c6uawQNowE

ALT Photo of 9 people: Dr Amanda Ruth - Director Corporate Affairs, Access & Policy, Apellis Australia, Ms Libby Croker MP, Dr Kathy Chapman - CEO of MDFA, Dr David Gillespie MP, Ms Meryl Swanson MP, Chris Edwards - Manager Government Relations & Advocacy, Vision Australia, Judy Hatswell - CEO of Sight For All, Julia Hall - CEO of Retina Australia, Carly Iles - CEO of Vision 2020 Australia
Retina Australia was delighted to engage with government, industry, health bodies, academia & advocacy groups at #PharmAus24 focusing on "Accelerating patient access to new medicines". Thanks to supporters of our awareness activities. #InheritedRetinalDisease
Join our community as members of Retina Australia or renew your membership, to support people affected by #inheritedretinaldisease. Two new benefits to members with our Membership Partners Optometrist Warehouse and @ChemistWhouse and Good Citizens Eyewear
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