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Home
The Science
Who We Are
Our Story
Values
Staff
Board of Directors
Community Advisory Board
Newsletters
In The Press
what we do
What We Do
What is Ocular Albinism
Research
Vision Heroes
Family Support
Project Vision Aid
Resources
Financials
Events
Sip to See Tea 2024 Photo Gallery
Sip to See, Springtime Tea 2024
The Beach Boys (2023)
Sip to See, Springtime Tea (2023)
Springtime, Tea Time! (2022)
AJ Croce "Croce Plays Croce" (2021)
Mother's Day Tea (2020)
A Night for Sight (2019)
Valentine High Tea & Boutique (2019)
10th World Symposium (2018)
Madaluxe Event (2018)
Andrea Bocelli (2018)
Winery Event (2018)
Concert with a Vision (2017)
Additional Past Events
Blog
Get Involved
Ways To Give
Matching Gifts
Legacy Giving
Contact
Partners
Accessibility Statement
Donate
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Our Story
Values
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Board of Directors
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Newsletters
In The Press
what we do
Back
What is Ocular Albinism
Research
Vision Heroes
Family Support
Project Vision Aid
Resources
Financials
Back
Sip to See Tea 2024 Photo Gallery
Sip to See, Springtime Tea 2024
The Beach Boys (2023)
Sip to See, Springtime Tea (2023)
Springtime, Tea Time! (2022)
AJ Croce "Croce Plays Croce" (2021)
Mother's Day Tea (2020)
A Night for Sight (2019)
Valentine High Tea & Boutique (2019)
10th World Symposium (2018)
Madaluxe Event (2018)
Andrea Bocelli (2018)
Winery Event (2018)
Concert with a Vision (2017)
Additional Past Events
Back
Ways To Give
Matching Gifts
Legacy Giving
Contact
Partners
Accessibility Statement
 
 


OUR MISSION:


FIND CURES


WE ARE DEDICATED TO CURING HEREDITARY CHILDHOOD BLINDNESS AND VISION DISORDERS.

 
Learn More
 


OUR STORY

In 1989, doctors predicted a dim future for Sam and Vivian Hardage’s son, who
was born with ocular albinism type 1 (OA1), a rare, but debilitating, genetic
eye disease. Ophthalmologists told them that there was “no treatment,” “no cure”
and “no hope.” Very little was known about the disorder because few scientists
were researching hereditary vision disorders.  

So, in 1991, the San Diego couple established the Vision of Children
Foundation...

Read More

> “The secret to change is to focus all of your energy not on fighting the old,
> but on building the new.”
> – Socrates”

What is ocular albinism (OA)? 
Human albinism can be divided broadly into two types, oculocutaneous albinism
(OCA) and ocular albinism (OA), where “oculo” means eye and cutaneous means
skin. These terms were devised in the late 1940s, when medical science was less
sophisticated than it is now. The terminology sounds simple, but in reality is
probably incorrect, since all forms of albinism have relative deficiencies of
pigment in the hair, skin, and eyes. Historically, ocular albinism is an
inherited disorder in which the eyes are deficient in the amount of melanin,
which gives the eye its color or pigment, while the skin and hair appear normal
or near normal in coloration.

Read more


OUR GOALS

1) To fund cutting-edge research focused on developing treatments and/or finding
cures for hereditary blindness

2) To provide education and support for a worldwide network of families affected
by vision disorders

3) To provide state-of-the-art vision aids to assist low-vision children in need

4) To honor young people who have overcome their vision challenges and are
living extraordinary lives by featuring them in Vision Heroes videos and blog
posts

info@visionofchildren.org 

12555 High Bluff Drive, Suite 330, San Diego, CA 92130



858.314.7927

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