Pushing for a Pathway, by Chris

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: Chris

Neuroendocrine Cancer Site: Lung

Hospital: Royal Free

We’re delighted to welcome Chris from Wiltshire, who has just joined our Neuroendocrine Cancer UK Ambassador team. Chris was diagnosed in February 2021 by a private lung specialist at the Spire Bristol Hospital, with a primary in his lung known as an Atypical Carcinoid. In terms of Lung NET classifications (sometimes called pulmonary NETS or bronchial NETS), there are 2 main classifications: TC (Typical Carcinoid) and AC (Atypical Carcinoid). These are differentiated by their KI67% score and Chris’s was Ki67 <5% … so AC. 
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Chris’s Story

Initial Diagnosis and Chemotherapy

I had a course of chemotherapy quite quickly after diagnosis, doing 4 out of 6 cycles of Carboplatin and Streptozocin but it was unsuccessful.  I asked for a second opinion at The Royal Free London but they didn’t think surgery was feasible. Luckily, one of the Consultant Thoracic surgeons – Dr Igor Saftic at Bristol Royal Infirmary – agreed to try to remove my main tumour and I credit him with saving my life. There’s always more than one way to approach cancer, in my experience. 

Lung Surgery and Complications

In Sept 2021 I had a right lung pneumonectomy followed by 5 weeks in the hospital and almost a month in ICU (intensive care unit) for a herniation of the heart, pneumonia, and an infection.  

Discovery of Bone Metastases

In August 2022, I started to get some back pain and was referred for an MRI Spine. Then an FDG-PET scan showed multiple sites of bone metastases including my spine, hips, shoulder, left leg, and the base of my skull. 

The Importance of Self-Advocacy

This is where I believe self-advocacy comes in. At this point, my local cancer team hadn’t consulted with The Royal Free London NET Centre of Excellence and as a result, told me that only radiotherapy to control pain was an option for me … and that my prognosis was around 12 months. 

Taking Charge of My Treatment

Naturally, I couldn’t accept this. I rang The Royal Free London myself and spoke with Prof Caplin, head of the team. We agreed to try both Lanreotide monthly injections and Everolimus, an oral targeted therapy. I didn’t tolerate Lanreotide very well so came off it – but I’ve tolerated Everolimus well so far and at the time of writing (August 2024) I remain on it. 

Living Day to Day

Today, I still take some strong opioids for pain relief but I’m living a fairly normal life. 
My employer has been fantastic. They understand I have good days and bad days, and hospital appointments – and being able to work keeps me mentally strong. 

Life and Passions

I used to be a keen footballer and cricketer but these days I enjoy watching rather than playing – but that doesn’t stop me from fundraising at these events too. I also enjoy exploring our beautiful coastline and countryside with my partner, Gemma, and our dog, Arnold. Being in nature definitely helps me. 

Becoming an Ambassador

So why be an Ambassador? Well, I find it incredible that our NHS still has no formal recognised pathway for neuroendocrine cancer patients. There should be a structured approach to diagnosis, treatment, and follow-up in place, as there are with other, more widely recognised cancers. In my view, it’s only earlier diagnoses that are going to make a difference to us – and we definitely need the ‘age box’ removed from the tick list. I was 34 and although I ticked all the other boxes for a cancer referral, it didn’t happen because I was ‘an under 40 normally fit and healthy person.’ I’m looking forward to helping try to change this. 
 Chris 
19.8.24

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

Do you have a story to share?

Sharing what you’re going through with others can be incredibly powerful, helping others to feel less alone, find hope and reassurance, and feel more confident and empowered.

If you have a story to share, we would love to hear from you.

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Share your story

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.

Please complete the form below to share your story.

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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