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The Swallows Australian Edition Magazine

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Even on the Gold<br />

Coast - Neil Raward<br />

At 73 years of age I believed that I was bullet<br />

proof, as I had never suffered any health<br />

problems, except for a knee replacement in<br />

2011. In February 2016 I noticed a lump under<br />

my chin and immediately visited my GP. After<br />

various scans and a biopsy by a ENT specialist,<br />

I was diagnosed with Squamous Cell<br />

Carcinoma of the left tonsil caused by the<br />

Human Papilloma Virus. Now what did all this<br />

mean? I had no idea of my problem or the<br />

treatment that would follow.<br />

I was referred to the Gold Coast University<br />

Hospital (GCUH) to undertake further tests as<br />

part of an ongoing Head and Neck Cancer<br />

program. During this initial program, I was<br />

subjected to further tests from the ENT team<br />

and there were talks provided by speech<br />

therapists and dieticians, after which I was<br />

referred to a Radiation Oncologist and a<br />

Medical Oncologist (35 sessions of<br />

radiotherapy and seven sessions of<br />

chemotherapy). I was still none the wiser of<br />

what lay ahead as there was no one available<br />

who could really tell me what all this meant and<br />

what changes my body would undergo.<br />

I will not go into great detail of the following few<br />

months – the changes my mouth and throat<br />

were undergoing ¬¬- was it a dream or reality?<br />

Loss of saliva and taste, horrendous radiation<br />

burns, being fed liquid through a stomach tube<br />

for four months, the loss of 18kgs in weight,<br />

being a social recluse – what more can a<br />

human body take? Although, throughout the<br />

treatment and recovery period, I remained very<br />

positive of the outcome. My dreams were<br />

rewarded in August 2016 when I was given the<br />

all clear. Although I still have five years of<br />

follow-up tests to be declared that I am in<br />

remission.<br />

I have always been a good communicator and<br />

decided from the beginning that I was going to<br />

keep my family and friends informed of the<br />

treatment, the changes to my body and my<br />

thoughts and feelings throughout the entire<br />

ordeal. In the 12 months since I was first<br />

diagnosed with the cancer I have produced 18<br />

bulletins entitled My Journey which to date total<br />

12,000 words and many photographs. Without<br />

the support and care from my wife throughout<br />

the program I believe that my recovery would<br />

not have been as successful as it was.<br />

<strong>The</strong> health professionals have used my bulletins<br />

for lectures to university students, students<br />

undertaking study for their Masters degrees<br />

have requested copies and a compilation of the<br />

bulletins into booklet form has been forwarded<br />

to many patients about to undergo treatment for<br />

throat cancer. I have recently completed a Head<br />

and Neck Cancer Peer Support Volunteer<br />

Program conducted by the GCUH which<br />

hopefully will allow me to be a support to those<br />

patients who are having difficulty in handling the<br />

treatment program.<br />

Many people who battle cancer do not confide<br />

with friends regarding their treatment. Some<br />

have spoken with me saying they wish that they<br />

had handled things differently by being<br />

forthcoming with their ongoing progress during<br />

their treatment. This, they say, was to allow for<br />

not sympathy but encouragement during their<br />

treatment.<br />

If any person would like a copy of My Journey<br />

please contact me at neil.raward@bigpond.com<br />

<strong>The</strong> document is there for all to read and<br />

hopefully for those unfortunate enough to be<br />

diagnosed with throat cancer to have an<br />

awareness of what lays ahead.<br />

37

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