I feel so helpless, wife been diagnosed with stage 4 cancer

Hi folks,

First post, please don't take this wrong but its a forum I never wanted to post in, yet our cards have been dealt and here I am.

It's likely to be a long post, my wife has been diagnosed at stage 4 and I'm struggling with my feelings and being strong for her and the kids. I've been thinking about how I can keep myself mentally strong, I have a call with a counsellor tomorrow, but have been thinking about writing a blog, but in the meantime, we have hit yet another bump in the road today and so I thought i would kick off by sharing our story, so apologies in advance for whats likely to be a long post.

It started on Boxing day - we had bought in quite a lot of food for in laws over Christmas, but with the rapidly changing lockdown rules, ended up not needing it, so we had a slap up cheese feast after the kids had gone to bed, but as she finished the plate, my wife started to get pains in the abdomen - we thought nothing of it as she has suffered on and off with IBS like symptoms all the time I've known her, but it didn't get better. Throughout January the symptoms got worse but were masked by a shoulder injury and the stress of home schooling. She spoke with the doctor who felt that it was muscular and the Ibuprofen was upsetting her stomach, but by March it had got to the point where she was struggling with the stairs (we live in 3 stories) and having to rest after any work. The final straw was when she was exhausted by cleaning out the rabbit and i insisted she called 111 and eventually presented herself in A & E.

She was in for 2 days, at first they thought it was gall bladder, but a series of tests ruled that out and finally on 29th March I was called in and we were hit like a run away train by the news that she had Stage 4 Cancer with unknown primary, but had extensive secondarys in her Liver and some in her lymph nodes and a lung secondary. We were absolutely stunned - the next days passed in a blur, with further investigation, biopsy, gastroscopy etc.

We had a consultation for a trial at a specialist hospital for molecular diagnostics (which we hope to get the results of in a week or so) and chemo was due to start. The oncologist and our consultant decided the likely cancer was Intrahepatic Cholangiocarcinoma, or Cancer of the bile duct (although still not officially diagnosed), but then the next bump, she started to swell in her abdomen. More tests, another stay in hospital revealed that it wasn't ascites or a big build up of fluid, but constriction of a lymph vessel stopping fluids circulating properly caused by a tumour pressing on it and the risk of not having chemo was deemed greater than the swelling and so finally we started and had our first session.

Now I know that you will expect me to say this, being married to her, but my wife is flipping amzing - she is so optimistic, so full of fight and we dubbed that fight back day - we know the situation is serious, but finally we could push back. I was so nervous about how the chemo would affect her, but she coped fantastically well but..... then her legs and feet started to swell badly and she really started to lose mobility which was a huge blow to her, but the hope was that as chemo progressed, the tumours would shrink some and release the vessal and deal with the swelling.

Today was supposed to be day 2 of chemo, but she had a bad blood result, high Liver enzymes, real concern at the swelling and they have said that they can't do chemo today which we are gutted about and I have just taken her back to hospital for assessment. I am so scared that we will not be able to have any treatment at all, she is deteriating so fast with the swelling that I am scared that she will not have options, but the very worst part is the not knowing what the situation is, the first 2 weeks after diagnosis were hell and we're back not knowing again.

I feel so helpless, i always want to try to make thigs right and I can't help her. She is only 44, never smoked, didn't drink much, has a reasonable diet, no family history, it shouldn't be happening to her.

Also we have 2 young children, aged 9 and 7 - they know that she is ill, but we haven't mentioned Cancer (both of my parents died from Cancer in the last few years so we don't want them thinking about Mummy dieing when thats not on our agenda at the moment, but I know at some point I'm likely to have to break their world and tell them about their Mummy's condition.

I just feel so helpless.

If any of you have made it to the bottom, well done, and sorry for going on, I think I may start that blog after all, but thanks for reading.

Much Love to you all

Si X

  • Hi David

    Thanks so much for your words, and yes you are so right he's done many things to make me proud. Especially since he served with the Royal Marines but nothing has come close to the pride I have for how he is handling this. 

    K x

  • I found your post as I'm visiting my friend today who was diagnosed at the beginning of lockdown and is struggling with chemo side effects. She has never mentioned what stage she has I only know it was bowel that spread to liver. I'm so sorry for what your family is going through and I hope your wife is able to still have enjoyment each day. My friend is not feeling pain at all but sickness and nausea and collapsing seem to a constant problems with her chemo. She has been told it's incurable so wants to continue with chemo to get as long as possible with her family her blood tests were fine but they still talk about stopping her treatment ! It's so hard to give support when you don't know what to say. 

  • [@Si_in_the_north]‍ 

    I just wanted to say Im so sorry to hear of your wife's diagnosis, and for everything you're going through right now. You sound incredible and I'm sure your wife is so very thankful for your support and love in this time. I dont have any advice I'm afraid, but I just wanted to reply and say I read your post with a very heavy heart, and I really hope your wife gets the treatment she deserves. Lots of love xxx

  • Hi there and thanks for your reply, it can be really difficult to have these conversations and I guess, everyone is different so all I would say is to try to be led by your friend.

    From our perspective, the very worst thing is to have friends who avoid us because they don't know what to say, so I'm sure that your friend will just be happy to see you and, as we have found, at times like this you really learn who are your good friends.

    Whilst everyone is different, I know that my wife is happy to discuss her health situation, but it's a very limited conversation because, to be frank, outside of her medical team, no one, however well meaning, can help with that but, what she really likes are those friends that talk to her and message her about day to day things, difficulties they have with their children's spellings, how annoying their husbands are because they are always doing DIY and not finishing things and so on - she really relishes that slice of normal life in a world where our normal is so very different to the one we had a few months ago.

    Good luck with the visit, I'm sure it will mean a lot to your friend.:happy:

  • Hi Newlife,

    Thanks for the note, its really appreciated. It seems daft to say it in such grim circumstances, but we are both so grateful for the love, support and concern that so many of our friends and family have shown us, some have really shown what amazing and true friends they are and in that respect we are truely blessed.

    For me personally, I am trying to be strong and keep a positive brave face on for all of the family, my lovely wife in particular, but I have found this forum really helpful as a little personal space that I can use to let my fears and worries out and I have been overwhelmed to talk to such amazing people who have responded, those who are sadly in the same boat as me and those who are just supportive.

    I guess if you look at my responses you'll see that I always talk a lot (my school reports said "Simon will never use 1 word when he can use 10 :laugh:), but, thats my long winded way of saying thank you so much for your kind words - they really do mean a lot!

    Keep smiling!

    Si