Our Programs

We strive to provide as many people as possible with the information and tools they need to ease the daily challenges that the visually impaired and their families face.

Our primary strategy is to identify and fund cutting-edge research focused on developing treatments and finding cures for hereditary blindness and vision disorders.

We are dedicated to inspiring, educating, and supporting a global community of families affected by hereditary blindness and vision disorders. In addition, we offer iPads and cutting-edge handheld video magnifiers to assist children with low vision, in an effort to ensure that these essential tools are accessible to families in need who cannot afford them.

Our Programs strive to give everyone a clear image of the world around them.

1

Vision Heroes

We seek out inspiring young people who have overcome their vision challenges. These Vision Heroes mentor and motivate others to persevere and reach their goals.

2

Family Support

Learning how to come to terms with a diagnosis can be one of the most difficult parts of vision loss. We feel it is necessary to provide answers and a network for anyone in need of support.

3

Project Vision Aid

We donate iPads and handheld magnifiers to kids with low vision to help them achieve their full potential.

WHAT WE’VE UNCOVERED

Research Results

Over the past three decades, VOC-Sponsored Researchers have:

  • Identified the gene mutation responsible for ocular albinism type 1 (OA1), an X-linked recessive disorder in which the retinal pigment epithelium lacks pigment, while the hair and skin appear normal.

  • Developed the first genetic test for OA, allowing for prenatal diagnosis and carrier screening.

  • Created an OA1 mouse model with many characteristics similar to those in human OA1.

  • Determined the biochemical features of the OA1 protein and its involvement in melanogenesis (the production of melanin, which gives color to skin, hair and the iris).

  • Studied the use of stem cells to regenerate damaged eye tissue in mice.

  • Demonstrated the efficacy of gene therapy for inherited eye diseases.

  • Efficiently corrected the genetic mutation responsible for OA in induced pluripotent stem cells retrieved from an OA1 patient.

Help us fundraise with Facebook!

Did you know the average Facebook Fundraiser raises at least $200?

With a Facebook Fundraiser, you can raise money directly on Facebook to help The Vision of Children Foundation find a cure for hereditary blindness and vision disorders.

Every big or small action helps advance the cause.

You can help ensure children with hereditary vision disorders have the support and the tools that they need to learn, grow, and look forward to a brighter future.