Friday, October 31, 2008

Bianca's wish comes true


By LUCY VICKERS - North Shore Times | Friday, 31 October 2008

EXPERIMENTING: Bianca White, 5, was delighted to spend time doing food experiments with Suzy Cato.

EXPERIMENTING: Bianca White, 5, was delighted to spend time doing food experiments with Suzy Cato.

Five-year-old Bianca White has to go into hospital once a month for intensive chemotherapy, blood transfusions and steroid treatments.

Yet she is rarely seen without a smile on her face.

Bianca, from Albany, was diagnosed with acute lymphoblastic leukaemia in June last year.

The following eight months saw her spend 106 days in hospital with infections.

One of her favourite things is to watch Suzy Cato’s Suzy’s World DVDs, which show science and food experiments.

So as part of the Make A Wish programme Bianca requested to spend time with the beloved children’s
personality.

She was picked up from her home and taken to The Quadrant where she got to bake three different kinds of cupcakes – one with full ingredients, one with no oil and one with no eggs.

And then they made some instant freezing icecream.

Bianca’s mum Lea says the day was "really brilliant, she had such a great time, the best day ever".

She says her daughter, who has a one-year-old sister Caitlyn, is a happy-go-lucky child who takes it in her stride and never complains.

At the moment she has to take chemo and antiviral preventative tablets every
day.

"She’s in the maintenance phase, which means looking out for and targeting hidden cells.

"It’s an ongoing treatment but hopefully she will be finished by September next year."

Saturday, October 18, 2008

Cancer battler Kyah still clinging to life


By TAMMY BUCKLEY and KRISTIAN SOUTH - Sunday News | Sunday, 19 October 2008

Brave cancer tot Kyah Milne was last night continuing to cling to life with her family by her side.

The two-year-old Wellington girl has captured the hearts of the nation, with her dedicated parents Shanell Christian and Jason Milne continuing to spend as much precious time with their daughter as she slowly dies of the neuroblastoma cancer that has riddled her body.

"We're now just really playing it hour by hour," Shanell told Sunday News yesterday.

"It used to be months, weeks, then it was days. Now we are into the hours every hour is a bonus.

"She is battling on but she's pretty sleepy, she's not doing a whole lot. We appreciate every hour we have with her now."

Sunday News last week told the story of little Kyah and her family's heart-wrenching plight, which is documented in an online journal written by Shanell.

The family had moved Kyah's third birthday party forward a month to last weekend, to give the hundreds of people touched by the precious youngster a chance to say goodbye.

"She wasn't expected to live past last weekend. We'd all resigned ourselves to saying goodbye but she's still here," Shanell said.

"She's playing by her own rules at the moment."

Shanell said the family were unsure how much longer Kyah could hold on.

Since our front-page article last Sunday, Kyah's online journal has become bombarded with messages of support.

"Her journal is getting so many hits. We used to get 14 or 15 comment but now we're in the 60s. The support is huge, absolutely huge."

Well-wishers have donated more than $2400 to the Child Cancer Foundation.


By HAYDEN DONNELL - North Shore Times | Tuesday, 14 October 2008

TUI SONG: Tui McLeod sang to raise money for the Child Cancer Foundation.

Child cancer donors have been drawn to open their wallets by a North Shore songbird.

Birkdale six-year-old Tui McLeod was diagnosed with a large tumour on her brain stem in May 2007 after waking up paralysed on her right side.

Surgery and long-running chemotherapy did not stop her giving her all to raise cash for the Child Cancer Foundation this month.

She sang her favourite tunes from Phantom of the Opera and interviewed celebrities at the foundation’s Cash Cube for Kids event.

Mum Deborah Lennon says cancer has not taken away Tui’s love of life or desire to be in the spotlight.

She wants to become an ambassador for the Child Cancer Foundation and she raises money for the foundation because it helped and supported her through her cancer journey.

"They’ve helped relieve the financial burdens and the emotional stress. It has just taken that pressure off," says Ms Lennon.

"There’s so many families out there that need support, they need this money."

A group of AUT students designed the Cash Cube for Kids event, which raised about $3500 for child cancer. They designed a brightly coloured cube to which people were encouraged to stick their donations.

Student Melanie Michels of Torbay says: "It was really rewarding interacting with the kids and raising money for such a good cause. It was also amazing to see how generous Aucklanders really are."

Wednesday, October 15, 2008

Cancer children coming home


By RUTH HILL - The Dominion Post | Thursday, 16 October 2008

KENT BLECHYNDEN/The Dominion Post

SETTLING IN: Wellington's new child cancer specialists Mwe Mwe Chao and her husband, Christian Kratz, don't have any patients yet. They toured the paediatric ward and met Victoria Jacobs, 7, who has rheumatoid arthritis.

There was no obvious upside when Wellington's two child cancer specialists quit.

But it did create a once-in-a-lifetime opportunity for one medical couple and Wellington now has two world-class clinicians.

United States-born specialist Mwe Mwe Chao said she and her husband, Christian Kratz, arrived on Sunday.

They worked together at the University of Freiberg Hospital in Germany and were in the unusual position of "looking for the same job in the same place".

"We thought it [New Zealand] would be a wonderful place to raise our family." The couple have a 21-month-old daughter, Matilda.

Dr Kratz said they were also excited at the prospect of rebuilding the service.

"All the staff are very motivated and there's a lot of positive energy."

With the resignation of Liz Hesketh in July last year, the unit - one of three child cancer centres in the country - was forced to send patients to Auckland or Christchurch.

The last remaining specialist, Anne Mitchell, stepped down in January.

Dr Chao said there were big challenges ahead.

"Part of the problem is New Zealand is small and paediatric oncology - fortunately - is also small, and that presents problems for practising physicians ...

"But I think the health board has done a really good job of organising everything, there's strong commitment from staff and everyone is ready to go."

Dr Kratz also plans to continue his world-leading research into the genetic origins of cancer.

The health board hopes to recruit a third specialist.

The couple hope all Wellington families will be home by the end of November.

Johnsonville mother Shanell Christian, whose daughter Kyah was diagnosed with cancer 15 months ago, said she was relieved that other families would not go through the same trauma her family had suffered. They were sent to Christchurch less than 24 hours after Kyah was diagnosed with a rare cancer of the adrenal glands.

She endured major surgery, chemotherapy and radiotherapy and weeks apart from her father, Jason Milne, and two brothers.

The family learned last month the cancer had returned and Kyah was unlikely to see her third birthday on November 3.

"We're just enjoying the days we have left with her," Ms Christian said.

"It's too late for us, but I'm so glad that other families will not have to go through the trauma we suffered.

"When you have a sick kid, you don't want to have to leave home."

Wellington's child cancer unit up and running again

New 7:56AM Thursday Oct 16, 2008

The arrival in Wellington this week of two paediatric oncologists means that the capital's child cancer patients can now be treated much closer to home.

United States-born specialist Mwe Mwe Chao and her husband, Christian Kratz, fill the void created by the resignation of Liz Hesketh in July last year and Anne Mitchell in January.

Their departures forced the unit - one of three child cancer centres in the country - to send patients to Auckland or Christchurch, splitting families at a traumatic time in their lives.

It is now hoped all Wellington families affected by child cancer will be home for treatment by the end of November.

The two world-class clinicians, who have come from Germany's University of Freiberg Hospital, were in the unusual position of "looking for the same job in the same place".

"We thought it (New Zealand) would be a wonderful place to raise our family," they told The Dominion Post.

Dr Kratz said they were also excited at the prospect of rebuilding the service.

"All the staff are very motivated and there's a lot of positive energy."

Dr Kratz also plans to continue his world-leading research into the genetic origins of cancer.

The health board still hopes to recruit a third specialist.

- NZPA

Saturday, October 11, 2008

Bittersweet birthday for cancer tot

Click here to read original article
The final celebration
KRISTIAN SOUTH - Sunday News | Sunday, 12 October 2008

TEARS flowed as "birthday" cheers rang out yesterday for New Zealand's bravest little girl, Kyah Milne.

It was hoped Kyah, two, would be the face of a child cancer campaign after it seemed she had gone into remission from a heart-wrenching battle with deadly neuroblastoma.

But the emotional rollercoaster of the Wellington tot's short life took a tragic twist as the disease came raging back last month.

Realising they had just days left with their precious daughter, Kyah's dad Jason Milne and mum Shanell Christian brought forward her third birthday to yesterday.

The couple was determined the event would be a celebration of Kyah's heroic life rather than a sad commemoration.

"We knew she wouldn't make it to see her third birthday, so we decided to bring it forward," Shanell told Sunday News.

"We were planning to have it next weekend but we don't think she'll even hold on for that long.

"People have come from all around the country to see Kyah," said Shanell.

"This is more about everybody having a chance to say goodbye.

"It's more about celebrating her life than her birthday," she said.

Shanell shared her daughter's highs and lows in an internet blog, titled Kyah's Journey.

It attracted hundreds of hits a day as supporters sought to be updated on the little girl's struggle with neuroblastoma a rare cancer of the adrenal glands mainly affecting children under five.

Those wellwishers united to help transform Kyah's Johnsonville home into a carnival yesterday complete with a petting zoo, a bouncy castle, professional face painters and a clown.

"We were thinking we would do something big for her, but like family big. Now we've got people from all around New Zealand, some of whom we've never met face-to-face, coming to celebrate Kyah's life," Shanell said.

"We only had five days to organise it and I wrote about that on my blog and before we knew it were were getting so many offers for so many people."

A bittersweet presence at the party was a string of beads, each one representing a procedure Kyah has been through.

She has endured major surgery, chemotherapy and radiotherapy. Every day she needs several doses of morphine to keep the pain at bay.

Jason and Shanell have shared their daughter's rollercoaster ride since she was diagnosed with cancer 15 months ago.

Less than a month ago, they believed Kyah was just weeks away from being in remission. But on September 16, they were were given the devastating news the cancer had returned terminally.

"We don't see it as losing Kyah," Shanell said. "We see that through all her treatments and therapy we had seven fantastic months with our baby girl. She was fantastic, she loved being the centre of attention.

"We even applied for her to be the face of next year's child cancer campaign. She was just a normal happy little girl for eight months and that is a time that we will always be able to cherish."

While the family are preparing to say goodbye to little Kyah, they are also working hard to ensure her brief but blazing life will create goodness and kindness for others.

They are fundraising for the Child Cancer Foundation and Ronald McDonald House.

"When Kyah was in hospital in Christchurch I don't think we could have survived without that network," Jason said.

"We almost didn't want to leave, because it was like leaving a part of your family. We could never do enough to say thank you."

TradeMe is running a continuous auction on behalf of Kyah's family, where buyers bid for the right to sign their username on a T-shirt before putting it back up for auction. They are hoping the scheme will raise $5000 for CCF.

And Kyah's big brothers Kaleb, 12, and Jordan, seven, have been growing their hair long so they can shave it off as a fundraiser.

"Last year I managed to raise $750," Kaleb said.

If you would like to make a donation please visit www.fundraiseonline.co.nz/kyahsjourney.

kyahsjourney.livejournal.com