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Support Lincoln's Journey Against Cancer

  • Yesterday was so HARD! - update written by Vikki

      19 October 2026
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    I haven't posted much about Link's journey with cancer as most updates have been shared, by a family member, on this Givealittle page. However, yesterday evening was hard.

    For the most part lately, he's been playing like a baby again. Some feeding positions are still sore for him, but he can happily play on his playmat again. It brings a sense of normality, and apart from the feeding tube and other medical bits hidden under his clothes, he doesn't look like a sick baby.

    Yesterday, after his top-up feed*, he vomited twice. Then, even after anti-nausea medication, he vomited twice more. Thankfully since then, he's kept breastmilk down but we have been too scared to give formula top-ups overnight.

    After that, I heard Sam say from the other room "Oh f*?k." Naturally, I panicked and asked what was wrong. After initially not wanting to tell me, he eventually said that while he was touching Link's hair, a chunk of it had fallen out.

    We both felt really emotional. Sometimes you almost forget that his little body is going through all of this.

    We try to remind ourselves that it's a side effect, not a symptom. Even so, it doesn't make it any easier.

    We find ourselves wondering how long he'll keep his beautiful ginger hair.

    Sometimes, it's the little things that hit the hardest. Yesterday, was one of those days.

    *Due to weight loss, Link's dietician suggested top-ups in addition to Vikki continuing to breastfeed. It may take some time to find a suitable milk option for Link's tummy.

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  • It's great news!

      17 October 2026
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    We have incredible news!! 😊

    The results of the genetic testing (biopsy) showed that Link doesn't have the markers for the high risk category. Instead of being on the wrong side of 50/50, they're much more optimistic of a positive outcome. Please keep sending good thoughts and positivity as we truly believe it is helping!

    Go Link 💖

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  • Huge milestone, go Link!

      16 October 2026
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    They have been given free reign over Linky and he's no longer an inpatient. They will still have to spend time at the hospital every day, for the forseeable future, but the apartment allows them to have special family time, without the interruptions. They have been advised on administration of meds and will settle into a routine soon enough. It's a huge milestone and a very welcome one.

    Vikki and Sam are truly overwhelmed by the love and support they're receiving. A special mention to their ANZ colleagues who coordinated a 'Bake Sale for Baby Link and whānau'. It was HUGE and well-attended. There were heaps of contributions from ANZ staff bakers and butter chicken makers, as well as pie donations from Puku Pies and sausage rolls etc from In-House Catering. A big thank you to all involved, you are incredible ❤️

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    • 16/10/2026 by Becs

      Really lovely to hear this, great progress. Keep it up wee Link ❤ x

  • A night away from hospital, a sense of normality

      14 October 2026
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    The biopsy that Link had yesterday went well and they collected the samples for genetic testing. Everything went smoothly and he was back in Vikki's arms and feeding, all before lunchtime.

    He isn't allowed any milk before a general anaesthetic and he definitely lets everyone know exactly how he feels about that 😳

    He has been very chatty and is highly entertained by his toys. His babbling and giggling is hopefully a sign that his pain has lessened. He is now more familiar with video chats and thoroughly enjoys regular interactions with Olivia, who is back in Wgtn. For those of you that have had a chance to chat with him over video call, I'm sure you would agree that it's the best feeling ❤️🧸❤️.

    Vikki and Link are trying a night at the apartment tonight where Sam has been staying. It's accommodation provided by the Bone Marrow Cancer Trust. It's similar to Ronald McDonald House but they have their own two bedroom apartment. I wonder if Sam is cooking up one of his lovely meals tonight?

    I'm sure it will allow them space to connect, breathe and have a night without beeps and observations. They left hospital with a grocery bag of medications so there is still a bunch of med admin for them to manage however they are incredibly strong parents and will do an amazing job!

    Please know that your contributions and thoughts are so generous and heartwarming. Vikki and Sam are so thankful and Link is rocking through this journey, he's the strongest baby boy!!

    Thanks for reading ❤️🧸❤️

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    • 15/10/2026 by Carrie

      This is awesome, well done Link! Hoping it's a really peaceful night for them all x

  • Brave little dude, rocking his SpongeBob outfit!

      12 October 2026
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    In the last two weeks, this little guy has had more tests, transfusions and surgeries, than anyone should have to go through. It was an incredible relief to hear that his body is responding well to the chemo!

    It was thought that they'd collected enough biopsy samples but unfortunately, Link will need the additional biopsy surgery tomorrow (Tuesday) and that means another general anaesthetic 🙁. They will aim to get enough sample from a tumour but if not, they may have to do a bone marrow aspiration. On a positive note, they want to get the sample before they shrink more! It is hoped that once this sample can be genetically tested, they will have confirmation of the type of cancer, which will ensure they are following the correct treatment plan.

    As per the plan, Link is having regular blood transfusions and won't be having chemo this week.

    Check out the photo of him having a pillow nap while his blood transfusion is happening, almost looks like he's saying "No more photos, Mum" 🫣

    Lastly, just a note to Olivia, who has returned to Wellington and started back at school. You are brave and courageous by managing all the recent changes and we're all really proud of you. You are in our thoughts also ❤️

    Keep sending positive vibes, especially for tomorrow's surgery ❤️🧸❤️

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  • Radioactive SpiderBoy

      11 October 2026
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    On Thursday, Link was injected with radioactive iodine in preparation for his MIBG scan on Friday. The procedure involves the combination of meta-iodobenzylguanidine with low-dose radioactive iodine to look for neuroblastoma. A scan takes images to show neuroendocrine tumours. This typically takes between 1 - 3 hours, which in Link's case was under general anaesthesia.

    They were also told that he'd need another surgery on Monday, under GA, to obtain more biopsy samples. The high concern while under GA, is managing his blood pressure so having two procedures requiring GA was tough news. Day-to-day, they seem to have found a sweet spot, a combination max dose of two, used simultaneously.

    The MIBG scan happened on Friday. The procedure went well, BP did rise again and he responded well to meds. He didn't require an ICU stay this time, which was a huge relief. After he woke, he was smiley with the nurses and enjoyed extra boob milk, after being nil by mouth for the morning.

    On Saturday they received some good news. They don't have to do surgery on Monday because they should actually have enough tissue after all. Let's hope that sample is sufficient for testing and he doesn't need that surgery to be repeated.

    More importantly, although the MIBG scan didn't really work well, from what they could see (compared to MRI and CT scans) it appears he is responding to the chemotherapy so thats great!

    Go Link!!

    They were able to bundle him up and enjoy freedom outside for a few hours ❤️

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  • Smiles for his big sister

      8 October 2026
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    🧸❤️🧸

    How gorgeous is this interaction between siblings?❤️🧸❤️

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    • 09/10/2026 by Carrie

      He's such a beautiful boy! Keeping him and all the family in my thoughts <3 hope every day brings smiles and joy x

  • Anyone for sunshine - update for Wed 7th Oct

      7 October 2026
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    Vikki and Sam have had family arrive from Wgtn and they brought down Link's buggy. They've been able to get out into the sunshine, taking short walks around Hagley Park and the surrounding area.

    This week, he will have a radioactive procedure that shows exactly where the cancer is throughout his tiny body. Today he started iodine, in preparation for Friday's procedure. Vikki mentioned that it will saturate his thyroid so the radioactive iodine they use for imaging won't stick to it 🫪

    As you're likely aware, Link has a "Hickman Line" which is a soft, tunneled central venous catheter inserted into a large vein in the chest for long-term intravenous access. It has two separate tubes that come off of it and just dangle about annoyingly. Despite being tucked away into his clothing, he manages to get them and likes to hold them as he falls falls asleep. Often, they'll tuck them away again, but the nurse will find him holding them again later during the night 🤣

    I'm incredibly proud of these two loving parents, who are strong and courageous. They're seeing positivity in moments when their world is crashing around them. They're living a nightmare that most of us cannot begin to comprehend. A big shout out to their care team at CHOC, thank you for all that you do.

    Once again, thank you for reading Link's story.

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  • Blood transfusion today - update for Sun 4th Oct

      4 October 2026
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    Link had a blood transfusion today, his tiny body absolutely exhausted from the treatments so far.

    Today was a low energy day, he played for a bit before running out of gas, poor poppet. He had his giant dragon friend and skeleton fish chewie for comfort as he rested.

    Thank you for your continued support for Link's journey, he is so loved 😍

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  • 'Spa Day' - update for Sat 3rd Oct

      3 October 2026
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    This little guy is a strong warrior!

    After his third round of chemo yesterday (Fri) it was important for Link to have a bit of a spa day and have his stickies and hand lines removed as much as possible. They were able to dress him in his clothes and and he looks less like a patient and more like their gorgeous little baby.

    With his hand wrapped around Mummy's finger, and his white noise machine, Link is able to sleep... until he's rudely disrupted for obs 🤷‍♀️. We hope that with the pain meds, he's able to have some good dreams and feel less of the aches that his tiny body has been dealt.

    The doctors confirmed that the cancer is in his bone marrow also, which was tough news. The treatment plan had factored that in already but still hard to have it confirmed.

    Unfortunately, Sam has picked up a cold and so Vikki and Link had a quiet day today. The hospital suggested a walk outside however their pram is in Wgtn and it also seemed a bit too cold for outside, so they did some laps around the ward!

    Olivia is able to spend time with him, making glove balloons of course and Link listens intently when Daddy reads him Hairy Maclary, it's about dogs after all!

    On behalf of Vikki, Sam and Olivia, thank you for reading and sharing their journey so far. Keep sending those positive vibes and messages of strength and love.

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    • 05/10/2026 by Ana

      Dear Vikki, Sam, Link and Olivia, sending prayers and thoughts from Masterton. I am a friend of Christine's and she has told me about your hard journey. My thoughts and prayers are with you all through this challenging time, as a mum myself I can't imagine how hard this must be. Even though we don't know each other, take comfort in knowing that there are many people praying for your boy and you all. X Love Ana

    • 05/10/2026 by Sunita

      I live in Christchurch and noticed you mentioned not having a pram. I’d be very happy to have a look around and see if I can track one down for you to use while you’re here. I know Jo (Air NZ Days) and have been following along, and I’m so sorry your little one is going through this. Please feel free to message me if a pram would be helpful — I’d be very happy to help in any way I can while you’re in Christchurch. I passed my number onto Jo also x

  • Out of ICU - update for Fri 2nd Oct

      2 October 2026
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    Vikki and Sam appreciate the sharing and love. Thank you to everyone that has sent a message of support, made a donation or is just thinking about them regularly.

    Link had a good rest overnight, and successful feeding with Vikki, falling asleep holding her finger.

    From an ICU perspective, he bounced back really well after his surgeries and chemo treatments on the first day. They are taking all the positivity and just this morning, has been moved out of ICU and back to the CHOC ward.

    Keep those good vibes rolling in.

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  • Link, our little champ - update for Thurs 1st Oct

      1 October 2026
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    On Wed 30th Sept, brave Link had surgery under general anesthetic. They inserted a Hickman IV line into his chest and took bone marrow samples. While in surgery, his blood pressure rose dangerously and an artillery line was inserted for continuous monitoring of his BP once in ICU.

    While in surgery, Vikki and Sam managed a walk through Hagley Park. It was a beautiful day but the reality of their new 'normal' meant it was incredibly difficult to watch other families with their babies. They both feel comforted by the care team, feelings of positive vibes from the coincidence of the connection with staff who have kids (and dog) with Link's names.

    Later on Wed, Link underwent his first round of chemotherapy. Even through all the procedures and treatments, he smiles up at Mum and Dad, showing he's a strong little warrior. Vikki and Sam both witnessed some incredibly scary moments before morning came. Overnight, his eyes swelled and his stomach also. He struggled to keep his feed down and a nasal gastric tube was inserted to relieve some yuck in his tummy. By morning, the care team were pleased with his status. This afternoon, Link has had a lighter, second round of chemo.

    All of this in the past two days, this kid is a champ!! Link will start collecting his beads, Olivia get smaller, matching ones too. Sam and Vikki are incredibly humbled by the generosity of so many, whether it be donating or simply writing a message of support. Please keep those good vibes heading their way.

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    • 02/10/2026 by Mel

      Piki te Ora Link ❤️