Who we are
CEO/Founder - Georgina Mason
I set up this charity five years after receiving a total colectomy (the removal of my entire large bowel).
At the tender age of 32, I had been to see my Doctor for blood in the toilet after each bowel motion.
My doctor dismissed me from her office, saying I had eaten something that had caused internal scratching.
I was sent home with ointment and told to stop being silly after getting upset.
I did not realise at this stage this was the first signs of Ulcerative colitis which, if not monitored and managed correctly, had a high risk of developing into Bowel Cancer.
Even though the symptoms persisted, I was too embarrassed to go back to a Doctor and carried on with work and raising my three year old daughter.
Four months after my initial doctor visit I was diagnosed with typhoid based salmonella food poisoning.
The combination of food poisoning and ulcerative colitis resulted in an emergency surgery to remove my colon which had swelled to the point it was going to perforate.
Seven months after my emergency surgery I received a call from the Hospital saying they had finally found a time for me to have a colonoscopy.
I had been on a waiting list since my first visit to A&E after contracting the Salmonella food poisoning.
This procedure would have detected the colitis if it was available to me when I first visited my doctor nearly a year before.
Founder/CEO Georgina Mason
Feature Articles from our
Georgina the day after bowel surgery, losing 20 kilos in two weeks
The waiting list for these life saving tests take too long in New Zealand as we don't have enough trained colorectal nurses and gastroenterologists here. The ones we do have often get poached and go over seas as there is an international shortage.
With the roll out of the Nationwide Bowel Screening Program, more bowel cancers will be detected. Unfortunately, the criteria for current screening is only available for those Kiwi's aged 60 to 74 years old. Only around 36% of bowel cancers registered in NZ are currently found in this age group.
This is why I have dedicated the rest of my life to help find complimentary ways to reduce colonoscopy waiting lists for those Kiwi's who do not qualify under the Government's screening criteria.
Find ways to help rehabilitate patients back to good health and prevent secondary illnesses, and find the latest treatments available worldwide that we can bring back and use here in New Zealand.
We need to make a difference here in New Zealand.
Each of us has a different journey to travel when it comes to Bowel Cancer. Some longer than others, some shorter than others and some fraught with obstacles and hurdles. Whatever your journey you can feel safe in the knowledge there is a huge network of surgeons, nurses and advocates out there to help you.
We have a network of colorectal surgeons and nurses that contribute content and advice to this website and to the Bowel Cancer Foundation Trust.
I have had a colostomy bag on my side, two major reversal surgeries to create an internal J-pouch, cried every time I set foot in a hospital, educated myself about ulcerative colitis and subsequent bowel cancer, learned what to eat and what not to eat and that exercise really does make a difference!
As a solo mum, the hardest part of my journey was at times not feeling strong enough to care for my daughter.
Nothing is more important than the strong network of family, friends and those who have travelled the path before you.
If you have stories to share as a patient, caregiver, nurse or surgeon I invite you to please contact me directly through our Contact page or via email (firstname.lastname@example.org). If we work together, donate together and help each other, we can all make a tremendous difference.