Lung Biopsy, by Davinya

By: Leanne Talbot

Posted on: 2 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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Name: Davinya

Neuroendocrine Cancer Site: Lung

Hospital: The Christie Hospital, Manchester

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Learning about my Lungs

I thought some of you would like to hear my experience of a lung biopsy in May 2024, in case anyone is worrying about it.  I had mine at Wythenshawe Hospital in Manchester which teams up with The Christie NHS NET Centre of Excellence.  

On arrival, I was quite nervous, not knowing what to expect or what exactly they were going to do. I had been told I would be sedated and wouldn’t remember any of the procedure. I was greeted by a lovely nurse who took my details and attached the cannula. She gave me the choice of my hand or my arm. She told me that the arm was less painful. The cannula went in smoothly with only a slight pinch.

I was then greeted by a junior doctor, who talked me through the procedure. We had a chat and a laugh and I felt more comfortable and less edgy. He took me into the procedure room. There were 7 people in there and it was a small room. I made a crack about sardines.

I was assured that they were all necessary and had a job to do. They all greeted me and I sat on the bed. The head nurse checked my details and ran through the procedure asking each person if they were prepped and ready. She then asked me to lie down. The doctor administered the first sedative which, to be honest, didn’t really do anything but to be fair, I was already feeling fairly calm and reassured. They then sprayed the throat-numbing spray down my throat. This was the worst part of the whole procedure, it tasted like rotten bananas!

Also, as my throat went numb it became difficult to swallow. They began the procedure and decided not to administer the sedative to make me drowsy and to be honest, I was glad. The whole process took about 45 minutes. There was no pain at all, the worst effect was like having a very irritating niggly cough.  Once I was done, I was wheeled into recovery, still wide awake. After my throat returned to its former non numb state, I had a cup of water then a cup of tea and a sandwich as I had been nil by mouth all day.

So all in all, it’s 5 hours post-biopsy and my throat is sore but apart from that, all is good. It wasn’t so bad after all. I hope this helps anyone out there who may be panicking about having the same.

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

You do not have to face this alone. Support is here when you are ready.

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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