Newly diagnosed and needing some hope

  • 4 replies
  • 167 subscribers
  • 253 views

Hi everyone - my lovely mum was diagnosed with primary lung cancer last week. She is T1a but unfortunately it’s already spread to the chest valves and a single lymph node. Although she’s 79, she’s super fit and healthy, as well as asymptomatic, aside from a swollen lymph node. 
Whilst the diagnosis was such a shock (it still is) and we were hardly jumping for joy, we left the appointment with the chest consultant and McMillan nurse actually feeling hopeful and even optimistic. The message was very much that whilst it’s incurable, it’s treatable. 

2 days later, I phoned the McMillan nurse. The dark thoughts were creeping in and I needed reassurance that I’d heard correctly. She reassured me that they’re very much looking at treating mum so she can live with this and that treatments can be highly effective. 

We’re currently waiting for the oncology appointment where we hope to get a treatment plan and we’re doing our best to remain positive because we were told to. We’ve been told by the medical professionals we’ve seen so far that we have plenty of reason TO feel hopeful and positive. 

Yet literally nobody else is. The people I’ve told reply back in the most negative of ways. Telling me they’re here for me “when the time comes.” Telling me stories of their own relative with the same thing who died after 2 months, to make the most of this Christmas and to be strong. 
Even my friend who is a nurse is being quite negative  I know people mean well but it’s so hard  

I’m not looking for false hope. Or burying my head in the sand. But I’m also trying not to write my mum off. Instead of feeling positive, I’m not expecting the oncologist to say anything encouraging anymore, despite being told otherwise. 

I feel bereft. I feel on the verge of a panic attack at all times, even though I’m doing my best to stay calm. I don’t really know what I’m hoping for here but just some glimmer of hope 

  • Hi  and a very warm welcome to the online community which I hope you'll find is both an informative and supportive place to be.

    I'm sorry to read about your mum's diagnosis and I know how much a cancer diagnosis can affect the whole family.

    I'm not a member of this group but noticed that your post hadn't had any replies. Responding to you will 'bump' it back to the top of the discussion list again.

    While you're waiting for replies, it would be great if you could put something about your mum's diagnosis and treatment to date into your profile as it really helps others when replying to you and also when looking for someone on a similar pathway. It also means that you don't have to keep repeating yourself. To do this click on your username and then select 'Profile'. You can amend it at any time and if you're not sure what to write you can take a look at mine by clicking on my username.

    Community Champion Badge

     "Never regret a day in your life, good days give you happiness, bad days give you experience"

  • I was diagnosed with the same level of cancer as your mum with one lymph node affected. I have had surgery  and chemo. The treatment plan will be tailor-made for your mum and you will feel more positive when it starts, I'm sure. My treatment began in July 23. MacMillan nurses are very helpful, especially when you're having a wobble and you need reassurance. Do you have a cancer centre? We have the Mustard Tree at Derriford Hospital. They have information booklets, counsellors and helpful courses and a lovely place to sit and have coffee if you arrive early for an appointment. By the way I'm 75 and doing very well.

  • That’s lovely to hear and thank you for replying. We now have an oncology appointment for next Tuesday, which I think will make us all feel more settled. We feel a bit adrift at the moment and there’s time for the intrusive thoughts to creep in. 
    I’m pleased to hear you’re doing well and I really hope that continues for a long time to come 

  • Hi HelenCG

    I am so very sorry that you have cause to be on here.

    Unfortunately people still hear lung cancer and assume it is an automatic death sentence.  This is no longer the case; over the last two decades  treatments have been developed plus 'older' treatments have been made kinder so less side effects.

    The only people you need to take notice of are your Mum's cancer team.  Have faith in their experience and knowledge.

    I wish you and your Mum the best possible outcomes.

    Kegsy x

    "If you are going through hell, keep going" ; Sir Winston Churchill
    " Cancer may take my life; however it will not become my life" Kegsy August 2011