What you need to know about Keratoconus…

This is a blinding condition affecting 1 in every 45 Maori and Pacifica children, many Asian and European children too. A 30 minute treatment stops it progressing but can not reverse the damage done.. 

  1. Watch short videos of people living with this condition.
  2. Access all of our latest blog posts.
  3. We send you a quarterly update on how the screening program is running and results of the screening.
stay updated

Video stories of people living with the disease & updates on screening

Free membership to Cone.org whānau

Subscription Form (#4)

Does your child have this disease?​

As parents, doctors and educators, we prioritize children’s academic success, physical health, and emotional well-being. Yet, one critical aspect often slips through the cracks: their vision. 

For many students, vision problems like keratoconus—a progressive thinning of the cornea—may go unnoticed, quietly impacting their ability to learn and participate fully in life.

What is Keratoconus? The no nonsense answer…

What is the Cone Screening program?

What next if your child is found to have possible keratoconus?

Because We Can

How do we help?

Cone.org is a screening program we run from our not-for-profit company. We are run only by donations and with volunteers. We aim to offer your children the ability to maintain their independence through maintaing their sight. We love what we do

  • Help prevent blindness
  • Offer a brighter future
  • Improve employment prospects
  • Help education and learning
Cute Family Picture

Every child deserves the chance to see a bright future—literally and figuratively. Let’s ensure their vision isn’t the one thing holding them back. 

9

Volunteers offering their professional skills and services

7,300+

Children needing screening every year in Rotorua alone

1 in 45

Maori children have this disease​
testimonials

Real people.
Real transformation

We are in the process of interviewing some of our customers and we will bring you these stories soon. Please sign up for Free Membership to get updated stories from people who have been on their keratoconus journey.

“I used to squint and look mad – now my eyes are open and I look and feel happier.”
TK, Rotorua
“I did not know that I had a disease, I thought that this was a normal part of being a teenager.”
SM, Rotorua
Join Us

Sign up for Free Membership called Cone.org whānau.

Get regular updates of stories of those who have this disease, their journey to a better future where their disease is now stable.

  • Raise awareness
  • Help access treatment
  • Help identify
  • For a better future
Subscription Form (#4)
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Donate your time to help our children

Young Girls Embracing while Standing on School Corridor
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Learn more detail on keratoconus.

We cover what keratoconus is, how it has affected some of my patients and in-depth understanding of the screening program and so much more. This is a disease that can run in families and there are a number of associated conditions that make it more likely that your child may get keratoconus.

the Cone.org Way

No child left behind, they all deserve a future with good vision.

Our Mission

We won’t stop until every
child in New Zealand has been screened

Subscription Form (#4)

We are starting in Rotorua but have a vision for all of New Zealand to be regularly screened for this disease. Sign up for our free membership to stay up to date on our progress, video highlights of people with this condition and other resources.