An impactful information film about Usher Syndrome made by Havas Lynx for Cure Usher to globally raise awareness.
We will let the video do the talking.
The annual Cure Usher Ball often plays videos throughout the evening. In 2025 a video of some of the fundraising from the year played to the guests. We are happy to share that video here as part of a thank you to those fundraisers.
This conversation is an honest, open look at Sharon’s journey with Usher Syndrome — the diagnosis, the challenges, the misconceptions, the impact on physical and mental health, and the strength she’s found along the way.
What year for our charity , actress Lisa McGrillis voices the highlights on this video shown at the 2024 Cure Usher Ball .
Dave Steele – The Blind Poet has written this piece using the words from parents who shared their experiences with Mark and Laura . The team at Signpost Productions kindly provided their time to film Dave.
This poem is to help raise awareness of the condition Usher Syndrome and highlight the emotional impact it has on families.
Captured all the work put in to getting the Cure Usher Ball 2024 in Newcastle on. They captured all of the amazing energy at the event that evening . Thank you guys .
Jo Milne who suffers from Ushers syndrome, was deaf from birth. She had bilateral cochlea implants fitted which allow her to hear for the first ever, this is the moment they are switched on!
Amelia, parent helping the usher community by raising awareness.