The stories that matter

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Fri, 03 Jun 2011 9:00a.m.

Zahnee Campbell

Zahnee Campbell

Zahnee Campbell has brown eyes, her favourite vegetables are potatoes, and she has a sparkly selection of Disney dresses hanging proudly on her violently pink bedroom wall.

So far she sounds like your typical five-year-old girl. But she's a five-year-old girl who is being failed, because she is so different.

Five years ago Zahnee was born with a facial vascular haemangioma - a large birthmark that covered much of her head and face. It was so severe that it affected the development of her right eye, so while the birthmark faded with age, the damage lasted. Her reduced vision means she compensates - her head tilts on an angle, she suffers constantly from headaches, and she sits on her chair in a twisted position.

As far as anyone can tell, Zahnee's is the only case in the country. To date, she has been seen by nine specialists, but there is no-one in New Zealand with the expertise to help her. It seems Zahnee's case is so unique, it's effectively been placed in the 'too hard' basket. She's been offered surgery here, but it's largely cosmetic, and won't fix her worsening posture and pain.

So rather than sit and accept what the authorities here suggested, her mother Jade searched the world for a specialist. After two years, she found a doctor who would do it. The cost for the medical care New Zealand is unable to provide? $50,000.

There is a possibility of receiving a grant from the government to assist with operation costs, but it's by no means guaranteed. The Campbells would still have to pay for the travel and accommodation costs, rehabilitation, post-op care... Even that is a stretch. As yet, they've have heard nothing from the Ministry of Health, despite their requests. Nothing from Tony Ryall, despite the phone calls and emails.

But what do you do if the only way of helping your child is raising that much money? You do what you must. So the Campbells have set about raising that money on their own, every cent of it. Five years of battling and it's not even close to being over.

I asked Jade about getting Zahnee to New York, there was no hiding her determination. She’ll get her there, with or without the Ministry’s help. Zahnee's school and the local community are rallying behind them, but $50,000 is a lot of cupcakes and raffles and mufti days.

And all the while Zahnee carries on with her life, largely oblivious of the political manoeuvrings going on around her.

Zahnee's self portrait on the wall of the classroom is a big blue blob. But it's a smiling blob. Her teacher says she laughs her head off in class.

During class runs to and from an old tree on a nearby field, Zahnee will race on against the rambunctious little boys - always trying, always pushing, and never giving up.

As she ran towards the tree for the second time, one of Zahnee's shoes came off. She stopped, struggled to get it back on, and as she did so the little boy who had been running next to her also stopped, and put his arm around her.

Together they finished their run, collapsing next to their classmates in exhausted heaps.

What lovely little kids.

We meet a lot of ratbags, bullies and bad guys in this job. But those run-ins are largely forgettable, because the unsavoury characters they involve are completely forgettable.

It's the stories like Zahnee Campbell's that remain in the mind, because those are the stories that really matter.

 

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Contributions to Zahnee's treatment can be made to 12-3217-0140729-00

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Comments

29 Jun 2011 02:44p.m.

Paula Farrell wrote:

Hello Campbell Live. Just wondered what was happening with Zahnee's case. Is there an update for the Tauranga girl in need of money for eye surgery? Thanks

08 Jun 2011 05:50a.m.

Jade wrote:

Hi Arto - yes thankyou it was. Thankyou for everyones support its so encouraging!

07 Jun 2011 08:55p.m.

Arto wrote:

Best of luck and aroha to you, young lady... I have donated $20 to your account.... I just hope the account numbers are the right ones....

05 Jun 2011 10:12p.m.

Julie wrote:

Hi Jade.. I see above that you've added notes here, so hopefully you see this.. I've just read a NZ Women's Weekly magazine from 15 January 2010.. and thought of your Daughter, after seeing the item on Campbell Live. In the magazine, on pages 30 & 31, there's an article about a baby who was diagnosed by a paediatrician with an 'Infantile Haemangioma' on her nose - and it was recommended that she see 'Professor Swee Tan, an internationally renowned expert on vascular birthmarks, based at Upper Hutt Hospital.' The article includes: ' Professor Tan carefully examined Heather and advised starting her on the drug Propanolol, which was originally designed to bring down high blood pressure. French doctors treating children with raised blood pressure noticed that strawberry marks, a common feature with the condition, faded away with its use. Professor Tan told Karen and Dave he'd had amazing results when using it on Kiwi patients with haemangioma's.' She was closely monitored, and 'almost immediately, the ball on her nose reduced in size and the flaming red colour began to fade. Her other two strawberry marks also faded. Heather stayed on the treatment and within weeks, the mark was almost gone.. ' The article includes that Professor Tan can be contacted through the Gilles McIndoe Research Institute, a special unit at Hutt Hospital - there's info here: http://www.gmri.org.nz/The-Proposed-Gillies-McIndoe-Research-Institute.27.0.html I'll send this info to Campbell Live too in case you don't see it here, so they can send it on to you. I truly hope this is of help.. it's worrying when our Children go through things like this.. my very best wishes to your Family..

05 Jun 2011 08:27a.m.

penny wrote:

Didnt we have a story a wee while ago where a babies op cost in the region of 2million donated thru the goverment.Theres a lot of children that need ops but cant afford it.I really do feel for this young girl and her family and hope they get the money they need.I will certainly donate.Kia kaha

04 Jun 2011 06:17p.m.

Shelley wrote:

What an amazing story, from such an inspirational family. I for one will be digging deep to help them out. I can only imagine the heartache of a first time Mum wanting nothing but the best for her child, and the cruelness that some people can show when faced with a person or child who looks 'different'. Jade, you are a strong woman, and I wish you and your family nothing but the best.

03 Jun 2011 02:53p.m.

Jade (Zahnees mum) wrote:

Hi Sue it is ASB

03 Jun 2011 11:33a.m.

serenity wrote:

an excellent book that might help? 'Relearning to see' - by Thomas R Quakenbush. it is really quite an incredible book for eyesight good luck with your little one!

03 Jun 2011 10:00a.m.

sue wrote:

what bank?

03 Jun 2011 09:47a.m.

Mary wrote:

Well done TV3 for exposing the NZ health system or lack of it. This story only touches the surface of Zahnees problems. We must all support this family to get Zahnee to New York sooner rather than later. Dig deep $10 each would go a long way.

Lachlan Forsyth

Lachlan Forsyth is a reporter for Campbell Live.


This blog lets him talk about the stories behind the stories, which is good, because otherwise his workmates would never shut him up.


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