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Help Natalie Beat Cancer and Keep Smiling

  • She fought till the end...

      13 September 2015
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    Surrounded by her family our beautiful sister, daughter, wife, cousin, niece and friend Natalie Paterson-Green passed away on Friday 11 September after a courageous battle with cancer. Although her life was cut short it brings us comfort that she lived her life to the absolute fullest. So many amazing memories that each of us will cherish and we thank her dearly for those.

    Thank you too to everyone here on her Givealittle Page that helped give Natalie hope and many more valuable months. We even managed to bring her pain down to pretty much just Panadol, so an incredible improvement.

    After a complication and blockage, Natalie was given just 2 days left to live on Monday 3 August. She didn't believe it, her long term partner Caleb proposed and we arranged their wedding at our family home for Saturday 8 August. It was incredible, better than any movie, a memory Caleb and the rest of us will never forget.

    Natalie survived many weeks in the Hospice, she loved life and understandably did not want to leave us. She was so brave...

    Her funeral will be this Tuesday 15 September 1pm at J Frasers & Sons Funeral home in Invercargill. Love you Nat. Xxx

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  • Flights have been booked for next trip to China

      10 July 2015
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    Flights have now been booked for Natalie, Gail and I to travel back to China for (hopefully) the last round of Next Generation PDT. We will be leaving on the 20 July, returning 31 July if there aren't any complications. We all hope that this will be the last round of treatment, then we can focus on getting Natalie's strength and health back. Thank you all again for your support. xxx

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  • Message from Natalie

      6 July 2015
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    Natalie has finally felt well enough to write a post on Facebook to everyone who has supported her, and continues to support her. Here is her message copied from Facebook...

    "This is way overdue, but I've been trying to wait for the right time to write this post.

    Thank you so much to everyone for your love and support as I'm going through this shiz house time. Thanks to everyone who donated to help my parents pay for the treatment I need in China... Words can not express how grateful I am for that. Your kindness is overwhelming...

    It's been a rough journey so far and I've still got a rough road ahead but I know I'm going to look back at this and laugh in cancers face knowing that I've kicked it's ass and thankful knowing that you guys helped me do that!"

    Mum and I will be travelling with Natalie to China in approximately two weeks for the (hopefully) last round of Next Generation Photo Dynamic Therapy.

    Thank you again for your continuing support during this tough time.

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  • Two surgeries down...

      16 June 2015

    Overdue for an update sorry! Natalie had a really, really bad week last week with unbearable pain, worst ever so far... So its pretty stressful for everyone involved with barely any sleep or a break for Natalie, Gail or Ralph. That being said, its not always constant and for the last few days her pain levels have been at only a 3 out of 10 - hopefully this means things are working, so very promising! Her first surgery went really well on Wednesday and they sealed off the blood supply to her tumor by pumping what I like to think of as kind of 'concrete' through the tubes, it was being feed by four arteries and a network of other veins. One of the only places in the world where they are doing this kind of surgery so pretty cool. The second surgery where they hammer the radiation 'seeds' into her bone wasn't so successful due to her anaesthetic wearing off too quickly (she has an incredibly high tolerance to drugs and setting all records) so they only got 50 seeds in. This has put her back a week unfortunately. The plan until this afternoon was to repeat the surgery tomorrow with her awake and just with local anaesthetic this time, but that has just now been moved to Friday. I think this will be a blessing in disguise as her bf Caleb will have arrived in China to provide her with additional comfort and support. Again, this is state of the art surgery, so very exciting that she is able to be a part of it. On another note, they have managed to drop her medication from around 95 pills a day to just 11 - awesome! Again, from the bottom of my heart thank you all for your support during this incredibly draining and stressful time. xxx

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  • PET Scan and Pain Treatment

      1 June 2015
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    On Saturday Natalie had a PET scan and great news, the tumour is contained to one area and showed all clear elsewhere. It is in two lymph nodes and a lot of the bone which sucks, but in one area around her tailbone and pelvis. The doctors feel that that cancer won’t ‘harm’ her, but the pain she is in will.

    On Sunday they had a long meeting with doctors discussing the plan they have put together for Natalie’s treatment and to deal with the pain. One option is Brachytherapy. Essentially it is a technology to target radiation specifically at the target tumour using small metal ‘seeds’ the size of a rice grain. They only radiate about 1-2 mm square so very specific. They will probably use somewhere between 60-120 seeds and these radiate continuously for several days until the half life runs out. The top specialist in China who bought this technology to China some 15 plus years ago will be performing the operation.

    The other treatment is TAE which essentially is similar to having an angiogram, but threading a tube through an artery to the tumour and then once there, putting a dose of high concentration dose of chemo down the tube. This is to try and release the pressure on the nerve (which is causing all the pain.) Very high chance that this will be successful.

    So this is a new plan on top of the NGPDT for the cancer (it is supplementary) and it is the only place in the world where this treatment is provided. There may be other countries where these technologies are known and understood but there are no treatment facilities.

    Natalie, Mum and Dad have a meeting with the professor Tuesday or Wednesday and hopefully the treatment date will be set for the following week. They may have to reschedule their travel plans to stay longer in China, but will just have to play it by ear.

    The technology that is being developed In China by Scott (their contact) and his companies is amazing in terms of the identification of even very small cancers (right down to individual cell level). We are so lucky that Natalie is now in their care, and thank you all for your continuing support, it's still a long journey ahead.

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  • First day of treatment

      29 May 2015
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    Natalie, Gail and Ralph arrived safely in Guangzhou Wednesday 28 May. A bit of a hairy flight with pain but they made it. Collected at airport by hospital staff, whisked through immigration and had her first appointments today. They are all super impressed with the level of care and professionalism they have received so far. Here's a short video for anyone interested of her taking her first drink of the sensitiser. Thursday will be the next stage. It's because of you guys that we've been able to pay for this first round of treatment, so thank you so much. There are still more treatments ahead, so please keep sharing Nat's Givealittle page. Thank you!

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  • Off to China on Wednesday!

      22 May 2015
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    It’s going to be a long journey but we have started! Flights have been booked for next Wednesday 27 May to Guangzhou China for my sister Natalie, Mum and Dad. For Natalie it will mean the first round of approximately three treatments of Next Generation Photodynamic Therapy (NGPDT). For more information visit http://www.nextgenerationpdt.com/. As far as I understand Clinical Trials for NGPDT have already started in Australia, but they have been doing it for years at this particular Chinese Hospital with great results.

    Obviously this treatment comes at a huge cost, and that’s not including flights and accommodation, so again, I would like to say a huge thank you to everyone who is helping play a part to keep Nat smiling. You have been just incredible... Together we will beat this! xxx

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  • Thank you for all your donations!

      12 May 2015
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    Natalie took this photo last night to say a huge thank you to everybody who has donated to her cause. So far she has been absolutely overwhelmed and brought to tears by the generosity of family, friends and even complete strangers. The support we have received has been incredible, so thank you from Natalie and all of us.

    Nat had a great weekend and was able to travel to Invercargill to spend some time at the family home - a huge turnaround from the pain she was in at the Dunedin Hospice a week ago, so thank you to the team there and also the Radiation team at Dunedin Hospital. So far she is well on track for the small window of opportunity where she will be painfree and healthy enough to travel on a long haul flight to China for further treatment. My parents Gail and Ralph are hoping to take her in approximately two weeks time.

    Once again, thank you all for your support and please keep sharing this Givealittle Page. xxx

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  • The Full Story

      3 May 2015
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    My sister Natalie is one of the most positive, caring and optimistic people I know. For example, when her long term boyfriend Caleb was diagnosed with thyroid cancer in 2011, she was at his side through all his treatments. When he heard the news he had testicular cancer the following year, she was by his side the entire time through intense chemotherapy with a smile on her face, holding his hand and telling him it would be alright. In the end it was, he survived and was given the all clear.

    Then, in a twisted turn of events, the worst case of bad luck, little over a year later it was Caleb’s turn to be there for Natalie when she too, at the age of 26 found out she had Cervical Cancer. Ever positive, and ever the optimist, Natalie never complained as she went through chemo-radiation therapy. There was no time to harvest her ovaries, but she came to terms with the fact that she might never be able to have children - living was the most important thing.

    To anyone who asked how she was Natalie would reply ‘Good thanks, how are you?’, but in reality she felt like she had the worst hangover ever, was dizzy and violently ill.

    When the tests came back that her cervix was clear of cancer we all celebrated and let the world know via Facebook. It was a real high time for us as a family. However, a few months later she developed intense pain in her hip that was almost unbearable. During numerous trips to different doctors and the emergency department her symptoms were explained as side effects of her previous treatments. Despite this and her weakened state Natalie persisted and got an MRI scan, confirming our worst fears - the cancer had spread into the muscles surrounding her hip bone, this time it wasn’t going to be such an easy fix, it was too late.

    Natalie underwent another intensive course of chemotherapy, much stronger than the last time and the type that you lose your hair. Natalie now had to face the fact that she was very sick and it was staring back at her every time she looked in the mirror. Incredibly brave, she put on her wig, slicked on some red lipstick and went out to face the world. Her wig made her feel like she was normal, that life was carrying on as normal.

    Heartbreakingly, after weeks of chemotherapy, scans showed that the chemo was having little effect. The cancer wasn't going away and the best option was surgery, one that only had a 25% chance of being successful and she would probably not ever be able to walk properly again. Saying goodbye to her as she went into the operating theatre was one of the hardest things we have had to do, but it was our best shot at saving her life. During the 8 hour surgery Natalie lost a kidney, around 90% of a hip muscle (psoas), had major blood vessels replaced with artificial ones and lost a serious amount of blood. Most importantly though, she survived and the operation was a success! We cracked open the champagne that day. There was just a little bit to ‘mop’ up which radiation and chemo should be able to do easily.

    After undergoing chemotherapy (again) for six weeks and withstanding increasing levels of pain, an MRI scan showed that the chemo had been unsuccessful and that a ruccurrence had sprung up against the base of her spine and was pushing against the major nerve that runs down her right leg (which explained the pain).

    At this stage, the doctors at the hospital said that Natalie is moving towards palliative care as they didn't believe there was anything else available for them to cure her. They refered her to the Otago Community Hospice to manage the pain and have started her on two weeks of radiation therapy in an effort to reduce her pain. Unfortunately Natalie’s cancer is causing her agony due to it’s location on the major nerves that come out of the spine. Morphine hasn’t worked and they are now using Methadone and Ketamine.

    Natalie, Caleb and our family are left with the decision to either admit defeat like the Dunedin Specialist’s or continue to fight on and explore alternative treatments. Natalie’s cancer, although recurrent, is very small and localised at the base of her spine. It hasn’t spread throughout her body or to her blood stream. Logically (in our minds anyway), this c-word is curable!

    With the drugs Natalie is on combined with the pain she is in and radiation, means that we as a family have been tasked with carrying on the battle. As best we could we have investigated all the options available to patients with cervical cancer around the world. We think we have found that in Targeted Next Generation Photodynamic Therapy, although we are still open to other options.

    We have already raised quite a lot of funds but would appreciate and welcome help from our family and friends to ensure that a) Nat gets enough courses of treatment and b) Natalie doesn’t travel alone overseas and she has a family member with her. Every little bit helps and lets Natalie know that she is not alone in this battle, we are an army behind her. xxx

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