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Running for Little Mia

Closed Fundraiser page created in the Health category by Erin McKenzie


$2,000 of $500 goal

Given by 34 generous donors in 4 weeks

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Lysosomal Diseases New Zealand is a charitable trust dedicated to improve contact between families affected by lysosomal diseases within Ne

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  Nationwide Treatment

Little Princee (the way she pronounces princess) Mia passed away in 2013 aged 3 to a rare Lysosomal Disease called MPS1 or Hurlers. Lysosomal diseases are inherited genetic defects resulting in enzyme deficiency which prevents cells from performing their natural recycling function leading to a variety of progressive physical/mental deterioration.

Lysosomal Diseases New Zealand is a charitable trust dedicated to improve contact between families affected by lysosomal diseases within New Zealand, and supporting research into the causes and treatment of lysosomal diseases and improvements in the clinical care of affected people.


Latest donations

  • Guest Donor

    Guest Donor on 30 Mar 2014

    Private

    Private

  • Fiona Anderson

    Fiona Anderson on 29 Mar 2014

    $110

    In loving memory of Mia.

    $110

  • ian dickson

    ian dickson on 29 Mar 2014

    $750

    Thank you for your efforts Ethan,Hayley,Erin .From MIAS family &friends in Australia.

    $750

  • Guest Donor

    Guest Donor on 29 Mar 2014

    Private

    Private

  • Sarah, Kyle, Nicholas, Beverley & Bruce

    Sarah, Kyle, Nicholas, Beverley & Bruce on 29 Mar 2014

    $100

    With love for the most beautiful little girl ever !

    $100


Who's involved?


Tax credit Donations of over $5 are eligible for a New Zealand charitable giving tax credit.
Page Moderated The page has been checked by our team to make sure it complies with our terms and conditions.

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This page was created on 28 Feb 2014 and closed on 30 Mar 2014.
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$2,000 of $500 goal

Given by 34 generous donors in 4 weeks

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