Thanks for visiting the Albinism Trust site. If you have questions which are unanswered from this content please email us.
Planning is underway for this years Regional Seminar and we invite you to come along on Saturday 17th November 2018. For further information please email email@example.com
To help us with our fund raising we have set up a new Givealittle site where people can make a donation if they are of a mind to. There is no charge for our services but we do need just a little money to do the essentials. Please click this logo to make a donation on line:-
Albinism Trust is voluntary not for profit group dedicated to New Zealanders with Albinism. We are not resourced for responding to International need, the two exceptions to this are collaboration with our Australian and South Pacific Island strategic colleagues.
From time to time we learn about young parents who have a new infant with Albinism and struggle to get their questions answered. The good thing is that we have young families in the group who are ready and willing to give advice or support if required. It is important for parents to be reassured and get answers they want. We firmly believe the Mums and Dads of babies with Albinism know their child best and Albinism Trust is here to help when or if called upon to do so. We also know that some families can struggle to get their head around lots of misinformation and ill informed advice about Albinism. We encourage people to talk about things and ask questions so they get the information they need to be reassured.
A copy of our 2014 Audio CD “Living with albinism“ can be obtained from the Blind Foundation library where it is listed as CD78973. Call Library Services on Free phone 0800 24 33 33.
Please email us at albinismATinspire.net.nz or use the contact form by clicking the button below :-
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