Throughout the day we had a series of posters posing important questions of interest to people with Stargardt’s disease. You can find out what the hints and tips were below. If you have any more to add you can email them to us and we can add them to the page.
For more information relating to any of the suggested support technologies below do contact your local low vision services or patient support organisation.
If you enjoy playing music: sight read music reader
CCTV readers
Lots of magnification
Get stronger
Ipad
The more you’re prepared to ask for help; the more you can do/achieve
People almost always like to help!
Early support in dealing with the diagnosis
More updates on what research is ongoing
Help with transition to university and careers advice
Occupational therapy and advice for university students on careers and support
Guides/leaflets should be more user-friendly and easier to use
Legal advice concerning reasonable adjustments at work - what are my rights?
Better communications
Information on how to accept the diagnosis
New resources and gadgets!
‘I feel I am all alone and the only person in my village/town with this condition’
Packages to support visually impaired people regarding mobile data. More data you have the more expensive it is.
Free TV licenses
Should I completely avoid eating Vitamin A?
More information on what is being done
How Stargardt’s progresses and what influences how quickly it develops?
Have leaflets updating patients on clinical trials and future plans
Clinicians should update more on what’s going on in the labs/clinic
How fast/slow disease progress? Any model?
Mechanisms of disease – mitigating and aggravating factors