To have one child diagnosed with Morquio A is heartbreaking. For the Horders, with two children, the impact is immeasurable – emotionally, physically, medically, socially and financially.
Our beautiful friends Max, 13 years, and Mila, 12 years, have an extremely rare disease that is damaging their bones, affecting their growth and mobility.
Max, 13, and his sister Mila, 12, have a rare hereditary condition called lysosomal storage disease which is damaging their bones, affecting their growth and mobility.
Their little brother asked: "Why can't we just go to the supermarket and buy them new bones?"
Funds Banked To
Martin and Janelle J Fowle
Campaign Creator
Janelle Fowle
Frenchs Forest, NSW
Fri, 29 Jul 2016
Deborah Hitchen
$100
I watched these two gorgeous little kids on The Project and was so moved by their story but also by how kind and caring they both were. I wish Max and Mila and your family nothing but the best. I hope from the bottom of my heart they get access to the medicine and treatment they need. Much love. xox
Mon, 18 Jul 2016
Adam Bonser
$100
Tue, 5 Jul 2016
Anonymous
$500
Wed, 29 Jun 2016
Anonymous
$300
Thu, 23 Jun 2016
carmel barber
$30
Ask all your supporters to petition the Government for the medication you need. Bless you kids. Hope they find a cure for this so you can run again.
Mon, 6 Jun 2016
Nigel and Cathy Wratten
$10
Sun, 29 May 2016
Karen Nitch
$200
We hope this can help towards getting the medicine you need, to help stop you're bodies feeling the pain from this degenerative disease.
Sun, 29 May 2016
Anonymous
$500
Sun, 29 May 2016
Simon Millar
$200
Thinking of Max and Mila and their family. Also will be signing the petition at: https://www.change.org/p/sussan-ley-the-pbac-need-to-approve-the-life-optimizing-treatment-of-vimizim-for-max-and-mila
Thu, 26 May 2016
Ruth Kerwood
$100
Thinking of you all....
Max and Mila, may you run and walk again one day without pain xx
SINCE Apr 2016
1228
Donations
$94,074 raised
TARGET $100,000
Please support this cause
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AUD
Fundraising For
Max and Mila Horder
Max, 13, and his sister Mila, 12, have a rare hereditary condition called lysosomal storage disease which is damaging their bones, affecting their growth and mobility.
Their little brother asked: "Why can't we just go to the supermarket and buy them new bones?"
I watched these two gorgeous little kids on The Project and was so moved by their story but also by how kind and caring they both were. I wish Max and Mila and your family nothing but the best. I hope from the bottom of my heart they get access to the medicine and treatment they need. Much love. xox