When it comes to your vision, any unexpected issue can make you feel vulnerable, as well as anxious about your ability to cope and eventually recover. So when a patient is given the initial diagnosis of Stargardt’s Disease, it can be alarming. Stargardt’s Disease is a rare genetic eye disease that occurs when fatty material builds up on the macula. Not only does that sound serious, but it’s also difficult for most people to understand. First, it’s important to point out that this is a rare disease and the chances of developing it are low. It is a genetic condition, and the disease should only appear if someone in your biological family has had it before.
The macula is the part of your retina that is sensitive to light and transmits sharp, clear images to the brain. The macular degeneration associated with Stargardt’s Disease is progressive, so your vision will gradually deteriorate over time. You won’t lose your sight entirely, but Stargardt Disease can make it harder to focus on things like computer screens, or the road in front of you. Typically, vision loss tends to begin in childhood, between the ages of 6 and 12. However, Stargardt’s Disease can also occur in adults who have lived their entire lives with no issues beforehand.