contact Us

You are very important and we want to hear from you. Please be aware that this is run by volunteers.

We will get to you as soon as possible but that this may take a few days. Get free resources and stay connected with 3 monthly updates on the screening program by getting Free Membership. SIGN UP FOR FREE MEMBERSHIP (Cone.org whānau).

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Get in touch

Feel free to contact us for any questions, we live to help others

We are passionate about getting the message out about keratoconus and we are striving to make screening of this disease as accurate, accessible, and available for all children in New Zealand.

No child left behind – every child deserves not to have to live with the severe effects of this disease. We want to eradicate the life limiting effects of advanced keratoconus. No excuses!

Daily our medical specialists deal with the devastating and restricting effects of keratoconus. A single painless scan of the eye to identify the disease and 30 minutes of treatment to stop this in its tracks. We are run by volunteers who are dedicated to getting help to your children.

We can only do this with your donations. We have no external funding and relay on the generosity of parents and concerned citizens to go out and educate people and provide the screening.

Contact Us

We’d love to
engage with you

We are run by volunteers to care for your children and to ensure that this sneaky disease if found and treated before it can hold your children back from their full potential in life.

Call Us

+ (64) 2108406871

Address

71-75 Fairy Springs Road, Fairy Springs, Rotorua, 3015

Email Us

hello@cone.org.nz

Get in touch

Frequently asked questions

Hopefully you may find some answers or inspiration here…

We are always in need for people to assist with organising the kids to line up and to get back to class when we perform the screening at schools.

We also have a need for volunteers to enter data onto the reports that are sent out to parents and referrals sent to the relevant eye clinics for children found to potentially have the keratoconus.

Use the contact form on this page to reach out to us and we will get back to you as soon as possible.

Our two priorities are to firstly raise awareness of this disease. This costs more than you can imagine. We run only on donations and cannot do what we do without the generosity of people like you. You probably donate toother causes, we just ask that you consider donating to us this month.

Please use the form on this page or phone Dr Colin Parsloe on 02108406871.

Trusted to ensure that no child is left behind

Specialist Ophthalmologist lead service

We are trusted eye care specialists already treating this disease in our clinic and hospital setting. We need to get into the schools to make a difference on those who have the disease and are not diagnosed yet.
We need your help – sign up to the free membership to get short videos of other children and adults experience on living with keratoconus.

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