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Natalie, Neuroendocrine Cancer Clinical Nurse Specialist

By: Leanne Talbot

Posted on: 5 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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I LOVE MY JOB

The impact of a cancer diagnosis is life changing, not only for the patient but also the people around them. I have had firsthand experience of losing a close family member to cancer, and it was that which started me on my journey to wanting to become an oncology nurse. Having experienced cancer from both a patient’s and family perspective, it helped me to understand the importance of the role of a key worker / Clinical Nurse Specialist (CNS) for patients and their support network. 

The impact of a cancer diagnosis varies from person to person and listening and understanding each person as an individual, is fundamental and the basic foundation to a CNS role. 

Having these skills equips me to provide tailored support, using a patient-centred approach.  I enjoy the variety in my work and I get great job satisfaction by being able to help patients and their families during such a difficult time. 

My first experience of supporting a patient with a Neuroendocrine Tumour (NET) was back in 2011, whilst working as an Upper GI CNS at a District General Hospital. At this time I had limited knowledge about NETs which posed some challenges. However, it was from this point that I developed an interest in the disease group, especially the variety of treatment options available. The opportunity arose to relocate to Manchester and join the specialist NET team at The Christie NHS Foundation Trust. Working at a specialist oncology centre had always been my dream and I feel very privileged to have the opportunity to join the NET team at The Christie and contribute to developing and improving patient care.

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.

Share your story
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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