Neuroendocrine Cancer and Sight Issues

By: Neuroendocrine Cancer UK

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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Name: Mel
Age: 74
Neuroendocrine Cancer Site: Primary in bowel, secondary liver initially

Mel’s Story

My name is Mel and I have neuroendocrine cancer which was diagnosed in 2014, along with prostate cancer. I am fortunate to be under the care of the Churchill hospital in Oxford, where I had bowel surgery and liver ablations in 2014. Since then I’ve had 4 weekly Lanrotide injections and recently I’ve had 4 cycles of PRRT. I consider myself very lucky because, apart from a few difficult abdomen episodes and the usual dietary and bowel issues, I lead a fairly normal and active life.

However, in April 2021 I woke up in the middle of the night and all I could see was black. I often wake at this time and I usually go to the toilet. I don’t turn any lights on because there is enough light from streetlights, but I couldn’t see the bedroom door so I didn’t know if it was open. As I could see normally during the day, I didn’t do anything about it for a week or two (perhaps I was being a bit fatalistic and put it down to ageing or something). However, as time went on, my sight during the day began to change; it took a long time to adjust from bright sunlight, a green shampoo bottle turned from green to orange and household lights which were normally white, had a reddish tinge. So I told my wife and decided it was time to do something.

My surgery told me to contact an optician but my local optician had a receptionist whose job was to protect the optician from patients (a throwback from the doctor’s receptionists of the 1950’s era) and as I didn’t want to wait 2 weeks for an appointment, I rang RNIB. I spoke to a couple of people there but they had no answers but suggested I call 111. They were very helpful and arranged for me to go the local Urgent Care Centre that morning. They too were very helpful and told me they couldn’t see anything sinister but arranged an appointment at my local hospital Eye clinic. This appointment was not helpful as I was told I had 6/6 acuity and there was nothing wrong with my eyes. I then contacted Moorfields Eye hospital via nurse led helpline. The nurse was unable to offer any solutions but suggested I should get my GP to refer me to Moorfields, so I contacted my GP and we agreed that I be referred to Moorfields. I was therefore surprised to get a letter advising of another appointment at the Eye clinic of my local hospital, from where I had apparently been reassured and discharged. My GP was also surprised.

In the meantime, my wife had been researching my problem, and Night Blindness can be caused by vitamin A deficiency, which in turn may be a result of malabsorption, the Lanreotide injections and Cholestagel,, (which compensates for the lack of a gall bladder). A vitamin A deficiency seemed a distinct possibility. But none of the eye health professionals seemed to believe this was the problem. I had also been to see an optician at Boots Opticians and she explained very clearly why my eyes were fine, i.e. no cataracts, no macular degeneration, no detached retina, etc.

In the belief that the appointment at the Eye clinic might not offer solutions, I rang NCUK and was lucky enough to speak to Cathy Bouvier; her reaction was that it sounded like Night Blindness! A simple blood test would show if that was the problem and because of the Covid induced problems and delays at the NHS, she provided information on private blood tests. The subsequent blood test showed I had a very low level of vitamin A. I then contacted Tara Whyand, a specialist NET dietician, who had given me good advice in the past, for advice on which supplement to take. I started taking a supplement on 8th June and by 13th June there was an improvement and by 24th June my sight seemed as it was prior to the sudden loss I experienced in early April. I was staggered and delighted at the rapid improvement.

I cannot thank Cathy enough for pointing me in the right direction and for the advice given by Tara. As with all things Neuroendocrine, it is sometimes difficult to get answers, so I relate this experience because if it helps just one other patient, then it will have been worth it.

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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