Recent strongly suspected colon cancer consult - early days but can’t sleep and panic all through nights

FormerMember
FormerMember
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Thanks for being there.

Monday saw consultant had sigmoidoscopy he said ‘something there that shouldn’t be’ ‘something nasty’ took biopsy but not waiting for results before booking mri, ct and colonoscopy. Copy of letter to gp confirmed suspected cancer.

Squeezed in for mri Monday, ct today, colonoscopy thurs next week got 3 days self isolating after COVID swab appointment Monday.

All a very big shock been reeling ever since. Only a few days but already feeling at times dread and panic and feeling of not being able to cope. Bloody hell, only start of journey going to go mad if I feel like this already.

Didn’t sleep Monday or Tuesday then so exhausted Weds night finally managed sleep after getting my poor partner Jason out of bed to calm yet another ‘Convinced death imminent’ rant and to stay by my side in the lounge until I drifted off.

Have had throbbing low back pain now two nights in a row and looking for solace with doc google only makes it worse. So worried it seems like bone met, which has robbed me of hope. Not bad pain, pain itself not keeping me awake and panic stricken more fear of what it means.

Desperate and lonely, have been leaning on boyfriend and messaging Mum at night since she is largely awake too. But don’t like to worry them more and tonight even when I think about going to either of them I just think ‘what’s the point, they love me but they can’t ultimately do or say anything to calm me.’ It’s so very lonely to feel the people who love you most in the world can’t shield you from terror.

I feel bad because I know there are people struggling to cope with harder parts of the journey, confirmed degrees of bad news, awful pain etc, but I’m just so desperate for help and don’t know where to turn.

Thanks for listening to my ramblings xx

  • Hi  and a warm welcome to the board from me. These early days of waiting for scan results, meetings etc. are very stressful but once you have a treatment plan in place then things will honestly feel a bit better.

    I shall give you my usual advice to new members which is to stay away from google - it is out of date, misleading and downright scary in places. Stay on here and the bowel cancer uk board - you can ask anything you want and there is nothing too daft or embarrassing - you can read other posts or click on people’s names and see their profile page. 
    Bowel cancer is notoriously slow growing but very treatable. It might be worth having a chat to your gp and seeing if they can prescribe you something to help you through these first few weeks. Everyone on the board will be happy to help and support you through this and the nurses on the support desk are available 7 days a week from 8-8 on 0808 808 00 00 if you need to chat.

    I was diagnosed in 2016 at stage 3 and went through my treatment with another couple of ladies and we’re all still cancer free. It’s tough mentally and physically but it is doable and I’m glad you’ve found us here.

    Take care

    Karen x

    Macmillan Support Line - 0808 808 00 00, 7 days a week between 8am-8pm
  • Hi Mactastic, please please take Karen 62 advice and do not google. I was like you well I still am because I googled and now I’m finding it hard to get anxiety under control. I am on antidepressants. The waiting is awful sending hugs Nelly55 xx

  • FormerMember
    FormerMember

    Hi never ever Google it was the worse thing I did. Now gey my info on here or from my cancer team. It's a hard long journey but find I go day by day can not think to far ahead. I have I am sure drove my wife mad many times but you be surprised how  much your love ones understand your moods. I am now pass my 3rd round of chemo and found the thought of it was more frightening than actually having it. All the best to you for  your appointments 

  • FormerMember
    FormerMember in reply to Kareno62

    Hi Karen,

    thanks so much for your message, I can’t tell you how much it means to me. You are of course right about Google and I have made a pact with myself to stay away now.

    I took a Kalm last night and after two attempts  to get settled and slip into sleep, with a kind practical chat with my partner Jason between, managed to drift off into sleep at around 11 and slept til 7.

    but i think it will be an idea as you say to speak with gap for sleeping tablets or whatever will see me though this period.

    as of yesterday have sore throat and wee cough, not constant on and off, so now worried I’ve COVID which will delay whole thing. Took home test yesterday all clear.

    I’m so very pleased for you and your couple of lady friends to hear your wonderful cancer fee news.

    thanks again

    mactastic

  • FormerMember
    FormerMember in reply to Nelly1955

    Hi nelly55,

    huge thanks for reaching out, every bit of support counts at the mo doesn’t it?

    so sorry to hear you’re in the same boat anxiety wise, do you find the ad are helping at all? I hope so.

    I got sleep last night after a bit of a struggle and am so grateful for that, but feel I might have to try the go route for something stronger than Kalms. 

    you take care and big hugs to you too. Sending you the biggest well wishes for the journey.

    mactastic

  • FormerMember
    FormerMember in reply to FormerMember

    Hi Allana1due,

    so kind of you to post for me, really appreciated.

    yes, getting the strong message from community that Google is a huge no no and will listen from now on.

    also trying as you say to go day to day, or sometimes when super struggling hour to hour or minute to minute.

    having to practice mental discipline in a few ways, it’s exhausting, I bet that’s something we can all relate to right now.

    I think you’re right about loved ones, I know if the tables were turned I would be there for Jason or my Mum no matter what. Just hate that they have to take this on with me. 

    thanks for sharing your experience of chemo and your kind words about the fear being worse than the reality.

    all the best to you too and take care

    mactastic

  • Hi Mactastic 

    I know exactly how you feel . It’s like your whole world is imploding and you can’t get out of your head . I just want to reassure you it does get better . It’s just that so much happens at once , ct scan , mri then the waiting game . I once you know the diagnosis and treatment  it gets easier . I’m a year from diagnosis and treatment and out the other side . I struggled so much at first I asked for help from doctor . I was put on antidepressants which took a while to kick in but eventually helped . Please if your struggling ask for help . You should have a number to ring so you can talk to someone. Sending a gentle hug and know you’re not alone XX

  • FormerMember
    FormerMember in reply to NellyB

    Hi NellyB,

    thanks for your message it really helps to hear, to know there is a world out there of folks who get it and care.

    can’t get out of your head is 100% right.

    so far in the day time and especially when have managed to sleep am far more able to be a bit closer to calm and to carry out small tasks like getting lunch or folding a wash load out of the dryer. Also to read or watch tv or listen to music and not feel I can’t focus or get anything out of it

    i will talk to go for sure, just got a bit of white coat phobia makes me shudder thinking of talking to anyone medical!

    really pleased for you to hear where you are on the journey and take care all the best

    mactastic xx

  • Oh Mactastic I know just what you mean about white coat syndrome.  Only have to look at a blood pressure monitor or talk to a dr my anxiety goes through the roof . I feel very out of control. I remember when i first got told it was cancer I just spent the next couple of weeks in a haze . I would sit and stare at he tv and take nothing in . I didn’t believe anyone when they told me it was going to be okay ( I’m mean how did they really know right?) I went to a very dark place . But you will find your strength , you WILL take one step at a time . Once you’re in the system you will be carried along . There is light at the end of the tunnel , you just can’t see it yet . Be kind to yourself , XX

  • Google can be a good place for other subjects. Whilst we may not have much control over disease processes, we do have the choice to find a degree of peace, whatever happens. I found tHearte mental anxiety worse than the pain at times. So mindfulness and living each day is something I point too. Finding gratitude for all the good I have had is also helpful. PeaceHeart I round stuff on Google about mindfulness.