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(showing 51 - 19  results found)

Stargardts

Stargardts diseaseStargardt’s Disease is an inherited eye disorder that causes loss of central vision at a young age. It affects the macula, the area of the eye responsible for central vision and seeing colour and fine details. The symptoms are very similar to Age-Related Macular Degeneration. Stargardt’s Disease causes progressive vision loss and, in some cases, near blindness.

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Strabismus

StrabismusStrabismus is an eye condition in which the eyes are not aligned properly and point in different directions. One eye may look straight ahead, while the other may turn inward, outward, downward or upward. The manner in which the eye turns may be consistent or it may vary. Which eye is straight and which eye turns may also differ.

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Usher Syndrome

Usher syndromeUsher Syndrome is the most common condition affecting both vision and hearing. It is a rare genetic disorder that is the main cause of deaf-blindness. The major symptoms of Usher Syndrome are loss of hearing and an eye condition called Retinitis Pigmentosa.

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LHON

Leber Hereditary Optic NeuropathyLeber's Hereditary Optic Neuropathy (LHON) is a genetic eye disease which leads to a sudden loss of central vision. While the condition usually emerges in a person's teens or twenties, rare  cases may appear in early childhood or later adulthood. For unknown reasons men are more affected than women.

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Albinism

AlbinismAlbinism refers to a group of conditions in which people have little or no pigment in their eyes, skin or hair. Albinism occurs due to inherited altered genes which do not make the usual amounts of pigment called ‘melanin’. Based on the amount of melanin in the eyes, different types of albinism can be distinguished. What the different types have in common is that they are all associated with vision problems.

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