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SARS-CoV-2 IgG Serology Testing

This assay can potentially be used to assess vaccine response and to detect previous infection.

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Media release: Where is the Pharmac Review Panel’s Report?

Patient advocacy groups and clinicians are calling out the Pharmac Review Panel for failing to get…

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Global Leukemia Patient Experience Survey 2021

The CLL Advocates Network is asking for you to contribute to the 2021 Global Leukemia Patient…

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CLL Advocates NZ is pleased to announce the official launch of its patient booklet, CLL – A Guide for Patients in New Zealand. It has been made available in both a digital download and as a hardcopy booklet. Click below to download, request a hardcopy and to learn more.

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Welcome to CLL Advocates NZ

My name is Neil Graham and I’m one of around 2000 New Zealanders living with CLL. I had a near death experience around 5 years ago. My life was saved by one of the extraordinary new treatments that are now available for CLL but which is not funded in New Zealand. You can read my story here.

I believe all life is precious, and I want others in the position I was in to have the chance to go on living. So I’ve set up this advocacy group to push for a mechanism to fund the therapy that saved my life and other innovative CLL medicines that are coming onstream.

This is going to be a straight-talking, no-frills organisation, and we want to complement the work of other organisations rather than duplicating the information and services they provide.

So I warmly invite you to subscribe to our website and join our private Facebook group where patients and their families can share stories and ideas. If you have suggestions on what we should be doing, or want to put questions to experts, or would like to write your own story for us to post on our Patients’ Stories page, we would welcome that. And if you’d like to get in touch see my contact details on this site. I hope that together we can make a difference.

Thanks!

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