November 14th 2019
Bowel Cancer New Zealand is pleased to see the bowel screening programme finally rolled out to half of New Zealand’s 20
District Health Boards. However, the charity is critical of how long it has taken, and how long it will continue to take
for the remaining half of New Zealand to get access to life-saving bowel screening.
Bowel Cancer NZ spokespersonMary Bradley says, “The pilot programme began in 2012 in Waitemata and proved itself within
two years. It is clear it is taking too long as only half the DHB’s have the programme at the end of 2019 and hundreds
of thousands of New Zealanders continue to miss out.
“It is encouraging that bowel cancer has been detected in 420 people since the launch in 2017, but heart breaking too,
as we know this is only the tip of the iceberg. For many of these people this diagnosis will lead to more timely
treatment and better outcomes. More people’s lives could be saved if screening was already nationwide, this is life or
death, we need screening nationwide now.”
Concerns have been raised by Bowel Cancer NZ since their Call to Action plan in 2010, over whether the workforce was
adequately resourced to cope with the increased demand a nationwide bowel cancer screening programme would bring.
Bradley says, “The Ministry of Health has dropped the ball on workforce planning for bowel screening even after repeated
warnings from our charity. If they had started in 2010 we would not be facing at least another two years before the rest
of the country gets bowel screening.
“We are still waiting to see a workforce capacity plan from the Ministry of Health which we assumed had been completed
years ago. To our shock, it emerged in the bowel screening review last year that one hadn’t been done.”
Early detection is critical in saving lives to bowel cancer. It is clear more investment needs to be put into the
screening programme to ensure it is rolled out as quickly as possible across the country and to bring the age down to 50
years old. It is also vital that bowel screening be available for Māori aged 50 and over now. Māori are directly
disadvantaged by screening starting at age 60 as a greater proportion are affected at a younger age.
Bowel Cancer NZ executive member Professor Sarah Derrett based at the University of Otago’s Department of Preventive and
Social Medicine says, “Bowel Cancer NZ is passionate about bowel cancer screening because we know it saves lives – and
the evidence of lives being saved for half of the country can be seen now.
“We want an end to the postcode lottery that currently exists around bowel screening and for all New Zealanders to have
access. Therefore it is imperative that the workforce capacity issue is addressed urgently, and that Māori enter the
screening programme at age 50 from now on to address unfairness in the system.”
Bowel Cancer New Zealand encourages open discussion about bowel cancer with medical professionals and avoiding ‘sitting
on your symptoms’. Symptoms include:
• Bleeding from the bottom or seeing blood in the toilet after a bowel motion;
• Change of bowel motions over several weeks that can come and go;
• Persistent or periodic severe pain the abdomen;
• A lump or mass in the abdomen;
• Tiredness and loss of weight for no particular reason;
• Anaemia.
About Bowel Cancer New Zealand
• Bowel Cancer New Zealand is a patient and family-led charity organisation.
• The registered charity was founded in 2010 by a group of people affected by bowel cancer, committed to improving
bowel cancer awareness and outcomes for people with the disease.
• Bowel Cancer New Zealand aims to provide clear and up-to-date information about the disease, symptoms, what to
do if diagnosed and to support patients and families affected by bowel cancer.
• The ultimate aim of Bowel Cancer New Zealand is to prevent lives being lost to this disease and to promote the
national screening program rollout in New Zealand.
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