You are still you, by Kath Lewis

By: Beth Chesser

Posted on: 6 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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Being diagnosed with neuroendocrine cancer tips life upside down (as will any type of cancer diagnosis) .It can take a long time to come to terms with, and not only is it a confusing and complex cancer, few seem to have heard of it either.

Furthermore, its a cancer that you know is probably incurable, which can in turn can have a big impact on your mental health; it can leave you feeling very alone and isolated, and you may even question if You are still You anymore?

When word gets round, you may notice that some people look at you and treat you differently, mainly I think because they are unsure of how to react,.  It scares them too.

But what do you see when you look at yourself?  What do they see when they look at you?  You haven’t changed as a person, you may have lost some weight, you may have gained some; you may have had surgery, you may not; you may be taking a whole medicine cabinet of drugs everyday, you may not.  Nevertheless, one of the most important things to remember in all this is that You are still You.

There are good days and bad days that can take many forms both physically and emotionally, and which can arrive quite unannounced with their own additional challenges.  Still, the person having to deal with these challenges is essentially the same person you were before diagnosis, dealing with everything that life throws at you in its own inevitable way, and often you will need additional help to do this; and if you do don’t be afraid to ask for it either.

Through it all though remember, You are still You, and yes some people will fall by the wayside as you travel on this part of your life’s journey, but those who stay also see that essentially You are still You too.

In the words of Brené Brown – “Owning our story and loving ourselves through that process is the bravest thing we’ll ever do.”

Voices of NCUK – https://www.neuroendocrinecancer.org.uk/supporting-you/voices-of-ncuk/

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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Published: 4 days ago

By Beth Chesser