Sunday, 27 August 2017

Cancer survivor is ‘getting on with life’

As New Zealand Cancer Society’s Daffodil Day push for cancer research funding has just come around again;

My friend Caroline Cornor believes the best thing for her to do after kicking cancer into touch is to, ‘get on with life and stop dwelling on the past’.
 
 
GOING FORWARD: Caroline Cornor is, 'getting on with life' after cancer and enjoying being a member of the Dargaville community, especially the Methodist Church.

Caroline tells her story because she champions the BreastScreen Aotearoa mammogram programme for revealing a pin-head sized aggressive tumour, despite BreastScreen’s usual disclaimer, giving women no guarantees of doing so.
She also wants to alay womens' fears about the disease as much as possible.
It all started when she went for her two-yearly mammogram - her last under the free screening system, at the mobile unit visiting Dargaville, on New Zealand’s Northland west coast.

About a fortnight later, BreastScreen rang her to say something on the mammogram needed further investigation.

“They wanted me to go to the breast centre in Whangarei. Another mammogram was done and I waited while it was being read. They said there was something there but they were unsure as to what it was.”

Next, a biopsy was taken that same day, which involved breast punctures.

“It was uncomfortable but not unbearable and I have a fairly high pain threshold. You could say it definitely stung but I was not in a lot of pain and no, I wasn’t afraid,” Caroline says.

She waited up to a fortnight again, for the biopsy result, which came back positive for cancer.

“I still wasn’t afraid, as I’m a fairly pragmatic person – what will be, will be.”

At that time, Caroline was told she needed to consult a surgeon and luckily, because of medical insurance, she was given a list of private surgeons she could choose from and she chose a woman who was born not far from where Caroline grew up.

“I spoke to another public hospital surgeon first and she talked me through it – telling me what might happen. She said, ‘if I were you, I would have a full mastectomy on the affected side’.

Caroline then attended an appointment with the private surgeon and during the consultation, this one also advised her to have the same procedure.

Health professionals told Caroline, then in her late 60s, the tumour was very small, it was a ‘young’ woman’s cancer and very aggressive.

“I have strong faith and I’ve been a member of the Methodist Church since birth.” she says.

The fortunate thing for Caroline, if it wasn’t for the original BreastScreen mammogram, it could have escaped into her lymph nodes.

A special x-ray in Auckland, showed no node involvement, which was a relief.

“Knowing that, I felt quite confident and comfortable that following the surgery, it would all be gone.”

Caroline was offered the surgery in about a week from diagnosis, but after getting some advice, she found she would not reduce her chances by putting it off and she elected to wait a month, to travel to see her children and grandchildren, in other parts of New Zealand.

On her return and before the surgery, she attended an oncology specialist, who explained the treatment following surgery and tests also found she was a good candidate for the cancer protein-inhibiting drug, herceptin.

She had the surgery in early December, 2015, followed by a course of six, three-weekly chemotherapy sessions, with herceptin. The herceptin application continued throughout 2016.

“I never thought I needed or wanted breast screening, because I’ve been fit and healthy all my life, except for coughs and colds. But now, I would definitely tell women to stop being scared of mammograms and stop scaring each other, telling stories about it being painful,” Caroline stresses.

She says it may be a little uncomfortable for some, but everyone is different.

“It is done for a good reason and well outweighs the alternative outcome. Because if this tiny tumour had not been picked up, I may not be here now.”

Her advice for anyone finding themselves in the same position:

“Take all the advice of the doctors and surgeons, in the public and private hospitals as they come up with the same answers.

And in Caroline’s experience, the public health professionals have as much access to state-of-the-art processess as their private counterparts. It’s just that the public workloads are greater.

Caroline is very positive when talking about the chemotherapy process.

Once again, everyone responds to these drugs differently but there are drugs given to people to combat any digestive challenges, which some can experience but not everybody.

“Some people don’t have any reaction to chemotherapy at all but I did have some challenges with keeping foods and liquids down after the second and third applications – but I found it was very much trial and error and I felt within myself, it’s like my brain was having an affect on my digestion.”

One doctor did tell Caroline some people have a centre in their brain that rejects medications.

Her family were proactive in assisting her to get on top of it, with one daughter researching the internet and another enquiring about public funding for help.

Her brother came and stayed for a few months, making sure she ate and drank.

She did have a couple of stays in hospital just to ensure her fluid levels were kept up and a blood transfusion was needed after the third chemotherapy session, when her platelets dropped too low.

Caroline also got a touch of pneumonia after the fourth application.

Due to the side effects, it was decided to abandon the fifth and sixth chemo treatments.

But even after all this, she says she would have rather gone through these difficulties, than not having the treatment.

Some people avoid cancer patients, because of awkwardness.

But Caroline encourages people to visit them.

Both in hospital and at home, people popping in to see her and asking after her, was a great morale booster.

“I don’t know if it was my own positivity that brought people in, or what but it was great to see them,” she says.

She is realistic about cancer generally and says no one gets an absolute assurance with the disease.

But she has been told, specialists don’t expect to see her again and to go on with her life.

By December 2017, it will be two years since the cancer was first found.

SIDE BAR

Caroline’s view on positivity, how to keep your strength up and getting plenty of rest, while going through treatments:

·        Some people may need help with showering, housework and meal preparation – because of tiredness

·        Try foods you usually like as you have to eat and drink. Try to keep your diet as balanced as possible.

·        Also, just get on with your life and try not to dwell on the past.
The Cancer Society says, 60 people a day in New Zealand, will hear the words 'you have cancer'.
 
 

 

 

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