Hi, I’m Nash, and I’ve got a rare syndrome. I need your help.
- $4,280.00 donated
- 55 generous donors
I’ll need lots of looking after all my life. Funds will go towards helping my parents with the extra costs of that
Hi, I’m Nash, and I’ve got a rare syndrome. I’ll need lots of looking after all my life. My cool-fun aunties set up this page in case you wanted to help.
I’m only little but I’m pretty special coz I’m the only person in New Zealand with Lesch-Nyhan syndrome. It means I’m sometimes a bit sore. And it can be hard to move properly or learn new stuff. But that’s OK coz I’ve got lots of family and friends around me who love me heaps.
**Update 05 July 2018: Our gorgeous Nash and his family have had a rough time of late. Only two weeks after his first birthday, it was discovered that Nash had developed a large number of kidney stones in his left kidney and was flown up to Starship hospital for surgery to remove them. The surgery went well and they removed SEVEN kidney stones that were affecting the function of his kidney. Nash went back home which was awesome for the whole family, but unfortunately after only a few days at home developed a high fever due to an internal infection. Nash was once again flown up to Starship hospital to undergo another surgery, this time to remove the stent from the previous surgery and to also insert a central line so that they could administer IV antibiotics to try and get the infection under control. We are all waiting with baited breath for signs of improvement so Nash can get back to feeling good again.
Our precious nephew Nash has recently been diagnosed with Lesch-Nyhan Syndrome (LNS). This heart-breaking condition means it’s unlikely he’ll ever walk, he’ll have developmental delays and the neurological and behavioural abnormalities he could experience include self-injury (biting and head-banging), muscle tensing and flailing limbs. And he may never learn how to talk properly too. We desperately want to help him and his family minimise the financial burden of this devastating condition.
Nash is a beautiful, angelic little boy with a smile that lights up the room. He has a big sister Jess (9) and brother Quinn (2) and they love him heaps! He is the gorgeous son of Francine and Nathan.
As Nash is still just 11 months old we are unsure as to the extent LNS will affect his quality of life. He is already over-producing uric acid, which is a symptom of LNS and could cause kidney stones and lead to renal failure in the future. We have been told that children with LNS have a life expectancy that doesn't often extend beyond their twenties. For all that time we know he will require 24/7 care.
The news has been a huge shock for Francine and Nathan and all of their extended family and friends. We want to bring together Nash’s support community and those who feel compelled to help the family during this difficult time.
We love this family so much and want nothing more than for Nash to have the most amazing life possible, and for the family to have super special experiences.
One-off or regular donations will help to cover the extra costs that will be incurred to fully care for Nash now and in the long-term future.
Thanks so much for your support.
For more information about Lesch-Nyhan syndrome you can visit:
Funds will be for expenses they may experience in order to care for Nash in the future, e.g wheelchair/s, doctors visits, medical and dental treatments, potential house renovations and a suitable disability vehicle, travel requirements to see specialists
Page created by:
Lucinda, Sonja & Therese Gulliver
We are Nash's aunties and we want him to have the best and most awesome chance at life, this is a way we can help the whole family to ensure he and they have the best care possible.
All funds raised benefit:
Funds will be paid to a verified bank account of FRANCINE GULLIVER on behalf of Nash Jones.
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