"I was not a man in my 60’s or 70’s – I was a 34 year-old female!"

5 minute read time.

 'Diagnosed at 34' written over a bench facing out to the sea at sunset.

Gina was diagnosed with lung cancer at just 34. She's kindly shared with the Community her experience of being diagnosed, and the shock and impact being diagnosed with cancer had on her at such a young age.

If, like Gina, you were diagnosed with cancer at a young age, go ahead and share your experiences with us in the comments section below. You might also like to visit our Diagnosed at a young age group to talk about and share your experiences with others of a similar age.

If you saw me walking down the street, it wouldn’t cross your mind that I have lung cancer would it? However, I am a growing statistic that seems to lack an awareness. It is becoming more and more common for young women to be diagnosed with lung cancer. Often, they have never smoked – so the usual red flags are out the window.

 We have all heard the campaigns about lung cancer. How if we have a persistent cough, cough up blood, or have rapid weight loss we should consult our GP – I had none of these symptoms. Having spoken to a fair few lung cancer patients, it turns out it really is common to NOT present with the classic symptoms we are told about. So how did I get diagnosed?

 I went to my GP about something completely different. I mentioned my other symptoms as almost an after-thought as I happened to be there. For me, they were discomfort in chest when lying on my right side at night, getting on two months, along with pains in my shoulder, numbness across my collar bone area and down the back of my arm coming and going, but now persistent. I had also on three occasions felt the whole right side of my face go completely numb for a few minutes for no apparent reason.

 I had googled the numbness and scared myself silly self-diagnosing. I had thought they might be looking for MS.

My GP suspected a trapped nerve in my neck, however he still was cautious and referred me for a neck and shoulder x-ray. I was a little surprised as I had absolutely no problems in my neck. Reading up on trapped nerves, I saw where he was coming from, and went for the x-rays which he promptly ordered.

 I didn’t think to note the other symptoms that had come on gradually during that time, as I had no reason to think they were linked, or that they were worth bothering the GP with. These were:

  • Sudden indigestion and belching – something I hadn’t ever had a problem with, and I just got indigestion remedies to try and ease it.
  • Fatigue – but I had always liked my sleep, but as time crept along I found I was exhausted after working all week and spent the weekends napping in the day, and sleeping well at night too.
  • Night sweats - this happened a handful of times, I never knew this could be potentially something to worry about. I just assumed I must have had a scary dream that I woke up not remembering.
  • I had been asked if I had coughed up blood, I said no. In hindsight I do remember coughing up slightly tinged pink phlegm. To me this was not ‘coughing up blood’ so alarm bells did not ring.

The x-ray didn’t show anything other than a slight narrowing of two vertebra. Chiropractic and physiotherapy treatment did not help, and the pain got worse over the next four months – so I went back and was referred for an MRI. A protruding disk was now suspected.

Within half an hour of getting out of the MRI I received a text to go that night for my results and to take someone with me. Much sooner than the scheduled appointment in a few days to receive the results. It was at this point my world came crashing down, I knew something desperately wrong must have been found. I wasn’t surprised to find it was more than a trapped nerve, the pain was excruciating by now. I was extremely surprised though, to hear that it was a large suspicious mass in the apex of my right lung.

I found myself desperately searching for answers whilst the never-ending diagnostic tests were going on in the background. I stumbled across information on Pancoast tumours and found they fitted exactly with my symptoms, all except the big but…I was not a man in my 60’s or 70’s – I was a 34 year-old female! How could this be?

'I have never sat and asked why me? Because why anybody? Nobody deserves cancer. For me, it has always been, why at my age?'

Gina riding a brown horse at the beach

For me, I have never sat and asked why me? Because why anybody? Nobody deserves cancer. For me, it has always been, why at my age?

It is easy to feel that you are the only one when you are diagnosed at a much younger age bracket to the norm. Though, sadly, there are many of us about dealing with a young cancer diagnosis. I found my worries may be very different to some of the usual lung cancer patients, that were more often at the retirement age or above.

I wondered, how would I let work know? How would I pay the bills if I couldn’t work? If I wanted to start a new relationship, when do you tell the person that you have cancer?

I can feel the curious looks when I walk into oncology, or take a seat in the chemotherapy chair. It can feel very isolating. If like me, you are a younger person being diagnosed, please know you are not alone. We are, sadly, becoming more common.

If you're a young person living with cancer, take a look at the range of information and support available on our website

Macmillan's here to support everyone affected by cancer. You can call our Support Line teams on 0808 808 0000 - available Monday through to Sunday, 8am to 8pm.

Anonymous
  • FormerMember
    FormerMember

    Gosh, all about me again so soon! Thank you for this Jimmy.  I will have to put my thinking cap on about to write about for a future one.. To be continued Grinning

  • I was diagnosed with womb cancer just before I was 38, they never suspended it because I was young, and its extremely rare in my age group. I didn't have all the common symptoms either, even my gynae oncologist was saying that he would not of expected what he saw. I thank you for making us aware of some of your symptoms Gina because like you say they are not the normal red flag symptoms. Doctors are learning all the time that our bodies react very differently and everything should be checked out completely.

  • Hi Gina,

    I know this feeling very well. Average onset of myeloma is 65 and all the brochures say getting it under 40 is “extremely rare”. But I’ve come to the conclusion that it is what it is. We are all dealt a hand and some are worse than others. 

    I do agree with you that a diagnosis in your 30s brings its unique challenges. I don’t think there is ever a good age to get cancer though. Sometimes I feel a bit caught in the middle. Young people’s cancers quite rightly attract a lot of attention. And when you’re older, it’s as if it’s more to be expected, so the medical teams are ready for you and support groups are already well established.

    In a way though, I’ve also seen benefits from being diagnosed relatively young. I was given the most aggressive treatment not given to most myeloma patients. I could almost see the consultant clapping his hands when I was walking in his direction, lol! The nurses have always glowed when I see them because someone my age is often quite rare on the ward. And whilst there is naturally loads of anger, frustration and jealousy towards my peer group that my eyes have been forcibly pinned open at this age, at least I am not stuck in that mindless place I was before all this kicked off. There are things I wouldn’t have done if it wasn’t for cancer and so it has not been all bad. 

    All the best

    Greg

  • FormerMember
    FormerMember

    Well done again Gina!  Very pertinent to the trend of younger people getting older peoples cancer. What does that say about our modern world ?

    The symptoms thing is also relevant as my sore knees symptom never gets a mention. 

    Keep up the good work.

    Albondigas x 

  • FormerMember
    FormerMember

    It makes it worse when you go for treatment and you’re sat next to some old codger with a copy of woman’s weekly and a flask :) maybe a touch of the stereotypes but I’ve had just that experience at clinics and it doesn’t help.  It’s tougher for younger cancer patients as life’s just generally tough these days anyway for most, and there’s things they may still want to do, whereas someone who’s eighty has had plenty of time to do everything. Harsh but it is a plain fact. Don’t get lost in all the doubts, worries and confusion.... look after yourself and at least one things for certain if you get diagnosed young, you’ll get every drug going and the surgery, on top of having all the strength to smash it up, so get smashing! 

    It was in my bones when I was diagnosed, skull, thigh and hip, then both lungs, 4 inch lump on my kidney - which was what it was, advanced renal cancer, and two random lumps floating about in my middle which are still there, as with the lump on my skull but they’ve shrunk. Kidney out, thigh bone/hip replaced, and lungs bits have shrunk to nothing, and that was with some spread after I changed onto a second line chemo. I’m now on my third line and fours years in. Can’t do cart wheels anymore because of my leg but I’m fitter than anyone I know. Perspective is just as important.