From GP to Fundraiser: Dougie’s Inspiring Story

By: Leanne Talbot

Posted on: 3 years ago

Trigger Warning.

Please note that while some stories end on a positive note, others may depict the challenging and difficult road that many neuroendocrine cancer patients face.

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Hi. I’m Dougie, a 59-year-old retired GP from South Lincolnshire, though originally from Edinburgh. I had a sub-acute small bowel obstruction and underwent an ileal resection just before the Covid lockdown in March 2020. Histology showed a Grade 2 NET.

Over the subsequent months, I had numerous trips to Peterborough and Royal Free hospitals for scans and tests. This was a very weird time as I was often the only passenger on the train to London. Initially, the tests were all negative, however, MRI in December 2020 showed liver metastases and I was started on monthly Lanreotide injections. These kept things stable until Summer 2022 when increased growth was found. 

I commenced PRRT in July 2022 and completed four treatments by February 2023. Thankfully my follow-up MRI scan showed stability. I’ve had minimal side-effects from the treatments although I do tend to squeal and swear a bit when I have the Lanreotide injection. Thirty-plus years of sticking needles into patients doesn’t seem to have helped me when I’m the one on the receiving end!

Despite dealing with many hundreds of cancer patients in my career, I saw very few with neuroendocrine cancer. In the early days after my diagnosis, I found the information available on the NCUK (Neuroendocrine Cancer UK) site an extremely valuable resource. I would now like to do my bit to raise funds for the charity, especially as I’m feeling fit and well at the moment. 

The Neuroendocrine UK Virtual Pathway Challenge appealed to me as I was a medical student in Aberdeen where the challenge started and the final walk is in Coventry where my son, Rory, now lives and works. 

My wife, Trish, and I plan to travel, in the words of The Proclaimers, 500 miles and 500 more before 10 November. We will be pounding the exercise bikes every morning and combining this with regular walks to hopefully exceed our target. 

Good Luck to all my fellow fundraisers and a huge thank you to everyone who has donated to this worthy cause. 

Dougie Burgess

 

You can sponsor Dougie here: https://neuroendocrinecanceruk.enthuse.com/pf/dougie-s-zebras 
You can join the Pathway Challenge here: https://neuroendocrinecanceruk.enthuse.com/cf/neuroendocrine-cancer-uk-virtual-pathway-challenge

Everyone’s experience of neuroendocrine cancer is different. Take your time, and engage with the stories in whatever way feels right for you.

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We’re always looking for people to share their experiences with Neuroendocrine Cancer. Whether you have the personal experience yourself or through a family member or friend, we use stories on our website, on social media, in our patient information, and on occasion, in the press.

By raising awareness of Neuroendocrine Cancer (NC), we can reach and help more people. Personal stories highlight many relevant aspects of living with NC.

Experiences provide insights that support the education of healthcare professionals, raise awareness of possible signs and symptoms pre diagnosis, raise awareness of NC in the general public arena and encourage and inspire other people who have just started their pathway.

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A note about reading and listening to personal stories

Everyone’s experience of neuroendocrine cancer is different. Some stories may offer hope and reassurance, while others may be difficult or upsetting to read or hear. Take your time, and engage with the stories in whatever way feels right for you.

Remember that treatments and outcomes vary from person to person. These stories offer personal perspectives and support, but should not replace advice from your own healthcare team. If something raises questions about your care, speak to your doctor or clinical nurse specialist.

Support and next steps

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Disclaimer

The stories and opinions shared here reflect the personal experiences and views of individual contributors and do not necessarily reflect those of Neuroendocrine Cancer UK. They are provided for information and support and are not a substitute for professional medical advice.


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