
Book recounts cancer journey
On June 15, 2023, the 62-year-old mother and grandmother was diagnosed with acute myeloid leukaemia (AML) at Southland Hospital.
After the shock diagnosis and trip to Dunedin for crucial treatment, Mrs Townson had the presence of mind to keep a diary of the journey she would weather for the next two years.
"It was when I tried to find something to read about what was going on, what to expect — I could find nothing."
She believed the lack of available information was due to fast-evolving haematology information and practices, which could quickly become outdated.
So she used her experiences to write a book that would help others.
"I wasn't going to write a book for a start, but I did start the diary.
"I'm not the sort of person that writes a book. I think it was therapeutic when I got home.
"There were lots of tears at times, and there was lots of laughter. My sons have all written their version of events at times when I was too high on morphine to know what the hell I was doing."
The limited-edition book was officially launched last Friday.
It was not just patients who walked the cancer journey, she said.
"You'll read why I've shared my story — [it's] not just support for me, support for all my family — it's s... for them too, going through this."
Her hairdressing business was closed, while her husband, Peter, took 12 months' unpaid leave from his job.
"It's been a very emotional time ... There's been a lot of changes."
She was pleased the Invercargill Public Library now had two copies of her My Shitty Gap Year available for the public.
Dunedin Hospital haematologist Dr Jared Williams' foreword said Mrs Townson took the initial diagnosis well and was only ever focused on fighting the disease.
He wrote: "The first round of chemotherapy was tough on Diane physically and mentally.
"She developed a life-threatening pneumonia and sepsis requiring a period in the intensive care unit where there was no guarantee she would make it through ... but she did and was all but only interested in pushing on. Diane's determination and grit was inspiration and she was tremendously supported by her husband Peter."
Mrs Townson said all the proceeds of her book sales would be donated to the Bone Marrow Cancer Trust and Leukaemia & Blood Cancer New Zealand.
The publishing cost of the 200 copies was paid for by crowdfunding. Copies can be bought by emailing dianetownson23@gmail.com
Hashtags

Try Our AI Features
Explore what Daily8 AI can do for you:
Comments
No comments yet...
Related Articles


Otago Daily Times
09-08-2025
- Otago Daily Times
Sliver of light after long battle
Closing in on a year since Wānaka woman Bronte Hardy was diagnosed with leukaemia, the mother of two says it has been one she would never want to repeat. After seven rounds of chemotherapy, over 20 blood transfusions and a stem cell replacement, Mrs Hardy is in remission and starting to see a sliver of light at the end of a long dark tunnel. Her shock diagnosis of acute myeloid leukaemia (AML) came last September, a day after her daughter's fourth birthday. Aalay is now 5 and her son Koby, is 7. "It's been a tough year all round really. It's all been low to be honest, it has been tough since the beginning and there haven't been too many positives." Her need to be in or near Dunedin Hospital during treatment, meant she had to undergo chemotherapy while her husband Shaun and their children, stayed living in Wānaka. The family travelled to the city on weekends and visited her at a place Mrs Hardy's parents rented in Dunedin. But looking back on the isolation, she doesn't know how she survived it. Mrs Hardy describes the eight-week-long stints in Dunedin under heavy treatment as "hell". She felt alone, frightened and "in a dark tunnel not knowing which way was out." Given the family had a plumbing business to run and a mortgage to pay, the couple made the decision for the family to travel over weekends with the children, and back to school during the week for normality sakes. "You never know what way is the right way when something like this happens, when really, I needed them there the whole time. You are just trying to survive." She felt further deflated when in January, her stem cell donor fell through because they failed a required second medical test. Mrs Hardy has a rare genetic mutation that would require her to go into remission and then receive stem cell treatment if she were to have any chance of survival. A donor was so hard to find. "Many people don't know they can be a donor, people know they can donate blood, which is a must." Mrs Hardy wanted people to know they can fill out their name on the register to be a stem cell donor with any NZ Blood service facility or doctor. Finally in April, a 75% match stem cell donor was found in Germany, and she was able to receive that quickly. Most remarkably, 100% of the stem cells have engrafted to her body, a success. "That is bloody good news" "I am in remission but you never know what is around the corner with blood cancer, but as far as I am concerned I am cancer free." News she needed, after watching her body change, her hair fall out, and life test her to the limit. "That is when you really learn to respect and love yourself. "All that positive reinforcement around you and having positive people and shutting out any kind of toxicity. When something like this happens in life, if there is any toxicity in your life it presents itself and you remove it." She urges others not to ignore the warning signs like she had. She said the body usually gives off signs, that we are all guilty of ignoring. "You can get so busy with life, especially in Wānaka, there is this constant hustle and bustle, never stopping, you are constantly working and constantly on the grind." Things have been on the up for the Hardys. The family has relocated to Christchurch, bought a new home and Mrs Hardy could be back at work as an interior designer within a year. "I knew I needed everyone here for me, I just knew I did for me to be able to heal. "Having family around you is healing. It is one of the best drugs around, having love and support." The 31-year-old is seeing this as a fresh start and an opportunity to change the way she lives life. "There is a silver lining in everything and I have taken positives out of this experience. It puts a lot of perspective on what's important. "It is important having your family around you and making those moments count, because it can all be taken away from you, in a sentence."

NZ Herald
08-08-2025
- NZ Herald
Auckland family struggles as both parents diagnosed with cancer
Their daughter, Victoria, told the Herald her parents are 'extremely scared' and overwhelmed by the uncertainty the future holds. 'He's worried about his family and what will happen, you know, how we're going to manage and stuff like that,' she said. 'Mum just wants to enjoy simple things with him, like going to the beach, without worrying. But he's very short of breath; he can't move far at all right now. 'It's horrible… we're just getting through day by day.' Kevin and Tracey are overwhelmed by the uncertainty the future holds as they both battle cancer. Photo / Givealittle 'He's a fighter': Lifetime of health battles Kevin is no stranger to dealing with health issues throughout his life, including multiple cancers and heart attacks. Victoria said Kevin, originally from New Zealand, was living in England but returned here with the family in search of more opportunities and a better lifestyle. Along with Victoria and her younger brother, they settled on the North Shore and hoped for a fresh start. Shortly after their arrival, Kevin's daughter from a previous marriage died from cancer at 13 years old. 'My dad has a genetic mutation linked to cancer, his mum had it, and our sister passed away from it too,' she said. 'It was very traumatic. 'Our sister had rhabdomyosarcoma, a type of cancer in the muscle behind the eye. Ten years later it returned as a brain tumour. She passed of cancerous meningitis at age 13.' Tracey (left) and her daughter Victoria, who says the family is trying to focus on the positives. Photo / Supplied Kevin suffered his first heart attack at 35 and was later diagnosed with prostate and bowel cancer, while Victoria was still in high school, she said. 'He was told he had a year to live when he was 50. But he's a fighter, he's always had this incredibly optimistic outlook, which I think has helped keep him going,' she said. Cancer fight and financial strain Six weeks ago, Kevin was hospitalised with Covid and pneumonia, but tests revealed he also had AML. 'It was touch and go, 50/50 whether he would survive that night,' Victoria said. Because of his weakened condition, his doctors advised that chemotherapy is not an option and the public health system can do no more for him, she said. 'The chemo would kill him. His body just wouldn't cope.' Victoria's older brother is visiting from Ireland for the first time in 10 years with his wife and three young children. The trip was made so they could spend time with Kevin while they still can. Kevin has been spending time with his grandchildren as Victoria's older brother is visiting from Ireland for the first time in 10 years with his wife and three young children. Photo / Supplied 'They just want some time with him. It's really hard knowing this might be the last chance they have together as a family,' Victoria said. With Kevin retired from his career as a draftsman, and Tracey forced to 'drastically reduce' her hours as a mental health nurse, the family is under financial pressure. 'Mum hasn't been able to work her normal shifts since her diagnosis. 'Mum did her first shift the other day but still worries about Dad the whole time,' Victoria said. Kevin was recently diagnosed with terminal acute myeloid leukemia after a history of cancer and illness throughout his life. Photo / Supplied The family set up a Givealittle page to help relieve the financial pressure they are facing. The money raised will go towards Kevin's special diet, supplements and alternative treatments, as well as everyday living costs. 'Those things are expensive, but they're giving him hope and maybe helping to extend his life, even if just a little,' she said. Victoria said: 'It's been really stressful because both of them have been unable to do stuff at times. So I've taken quite a bit of time off work. 'I'm not really sleeping… We are just trying to get through each day and focus on the positives.' The family is appreciative of the help it has received so far from the community. Sign up to The Daily H, a free newsletter curated by our editors and delivered straight to your inbox every weekday.


Scoop
22-07-2025
- Scoop
UN Experts Urge Taliban To Release Older British Couple Held In Underground Cells, As Their Health Deteriorates
GENEVA (21 July 2025) - A group of human rights experts* today expressed alarm at the deteriorating health of Peter and Barbie Reynolds, two older British nationals arbitrarily detained in Afghanistan without charges since February, calling for their release and immediate access to medical treatment. 'Peter and Barbie Reynolds have been held for over five months, including in a maximum-security facility for several months and later in underground cells, without sunlight, before being moved to above-ground cells last week at the General Directorate of Intelligence in Kabul. Their physical and mental health is deteriorating rapidly. Without access to adequate medical care, they are at risk of irreparable harm or even death,' the experts said. 'Our first demand is their immediate transfer to a civilian hospital for medical treatment,' they said. Peter Reynolds needs heart medication after suffering a transient ischemic attack in 2023. During his detention, he has had two eye infections and has intermittent tremors in his head and down his left arm, for which there are grave concerns given his underlying medical condition. He recently collapsed. Barbie Reynolds suffers from anaemia and remains weak and frail, potentially caused by months of poor quality and quantity of food. She also reported that her feet have become numb. The two individuals, who are married, aged 80 and 75 respectively, have lived continuously in Afghanistan for the past 18 years, where they founded a research and training business that provided training services to various companies and organisations throughout the country. They have been deprived of liberty in very difficult conditions without proper legal proceedings. 'We see no reason why this older couple should be detained at all, and have requested an immediate review of the grounds of their detention,' the experts said. 'It is inhumane to keep them locked up in such degrading conditions and more worrying when their health is so fragile.' The experts noted that Mr and Mrs Reynolds were reportedly detained without formal charges, have had no access to effective legal assistance nor medical care, and could only have very limited contact with their family by telephone. 'We remind the Taliban that all persons deprived of liberty must be treated with humanity and dignity, and that conditions and locations of detention must take into account their age and health circumstances,' they said. 'The psychological toll on their health from not knowing why they are being held or when they are to be released is cruel treatment.' The UN Experts have raised this case with the Taliban, the de facto authorities in Afghanistan, and the United Kingdom. They will continue to monitor the situation. *The experts: Alice Jill Edwards, the Special Rapporteur on Torture and other Cruel, Inhuman or Degrading Treatment or Punishment; Richard Bennett, the Special Rapporteur on the situation of human rights in Afghanistan; Morris Tidball-Binz, the Special Rapporteur on extrajudicial, summary or arbitrary executions; Claudia Mahler, the Independent Expert on the enjoyment of all human rights by older persons; Tlaleng Mofokeng, the Special Rapporteur on the right of everyone to the enjoyment of the highest attainable standard of physical and mental health.