Finished breast cancer treatment

Hi everyone, 

As the title says, I’ve recently finished treatment for stage 1 breast cancer. Everything went as well as it could have done. Stage 1, cancer cells weren’t present in my lymph nodes etc. but now I’ve completed radio, I think it’s all hitting me now how serious this has all been. I think I’ve been in auto pilot since finding out and now I feel a bit ‘out in the cold‘ if that makes sense as treatment has been completed. 

I’ll be seeing my consultant in the next 6-10 weeks to see how everything is going but I’m panicking the cancer may have spread and wasn’t picked up but mostly im terrified it’s growing somewhere else that I don’t know about. I have young children and the thought of cancer growing somewhere else just fills me with panic. 

is this normal? Is there anything I can do to ease this? 

thank you for reading xxx

Parents
  • Rolo 

    well done for finishing everything, I finished one year ago had my first annual check in July all clear .

    I don’t think the fear of reoccurrence ever goes away to be honest , I also think only a mamo once a year is not enough as it can come back anywhere in the body just not the best I feel we should get annual MRIS .this is something iM going to do next year is pay private for these every year gunna be my own doctor to make sure . 
    Love Lara x 

  • Thanks for replying Lara I really appreciate it and agree the mammograms are not enough. I really like the idea of having a private mri, out of interest do you know roughly the cost of that privately? 
    thanks again for replying and glad you are all clear xx

  • Rolo 

    yes k definitely bring my own doctor my 2 nd annual check is July 24 I’m going to book a private mri around this time full body I’m taking no risks xx I’m not to sure on price but think it’s about £600 to £800  xx 

    m argument is normally breast cancer comes back bones ect why don’t they carry out these tests annually too x 

    how are you feeling now ? 

  • I had bilateral mastectomies last September ,lymphclearance on left as well .Finished chemo in March and feeling great .It I is odd to finish everything though as we get used to going to all these appointments and also meeting people . I don’t have scans or mammograms as there is nothing now . I try not to think about secondaries as that would drive you mad . I do take antidepressants,mainly for the sweats ,and I take Letrezole ,which is like Tamoxifen but for post menopausal women . Suppose to take that for 10 years . Stay positive and live your life to the full xx

  • Thanks Lara and sorry for a delayed response. I’m feeling ok one day and terribly depressed the next. It’s just crazy. Not helping my elderly dog has just been diagnosed with cancer and only has weeks left. Everything seems to have happened at once this year and I’m struggling to take it all in. 

    Thank you for the info on the MRI, that’s really helpful. 

    Hope you are well xxx

  • Thank you for your message and sharing xxx completely agree about the secondaries. That’s what gets me the most xxx

  • Hi Rolo,

    This is a dilemma that we all face after our hospital treatment finishes. I am glad to hear that your treatment went well. Tamoxifen does affect your emotions quite dramatically, so we have to make some allowances for that. The fear of reoccurrence is something that we all have, but when we are tied up with diagnosis and treatment, we don't have time to give it much thought. It is only after all this finishes that the fear becomes a very real reality. This is something that we all have to live with and come to terms with, in our own individual ways.  Most people are seen and screened annually for the first 5 years after surgery. If you suspect anything untoward, you can always phone your breast care nurse and get checked over. 

    With regard to the seriousness of what you've been through. After the initial shock of diagnosis, we tend to get dragged along with the tide of tests, diagnosis, surgery and treatment, living from day to day, without having much time or energy to think about this. Once everything stops, it only then begins to really hit us.  The good thing is that this is all behind you now and you can get back to a normal life. We tend to make friends and get caught up in the social aspect of meeting others when we are attending hospital and many find it a lonely place when this suddenly stops. 

    Have you thought of joining one of your local cancer support groups? Somewhere like Maggie's or the Haven spring to mind. These are dotted all around the country and are an invaluable resource to have. If you don't have either of these close to you, there are a number of other charitable cancer organisations. You can pop in for a cuppa and a chat, talk to a nurse or a counsellor, attend classes on self care after cancer, join walking groups for people of different abilities, join a seated yoga class, avail of some  relaxing alternative therapies( such as reflexology, Indian head massage, aromatherapy, to name but a few) - all of these services even tend to be free of charge. Many people form their own self-help groups and arrange various activities which suit their particular group. Meeting up with others who have been through "the cancer experience" and being able to talk to them openly is one of the best therapies you can have.  

    I fully agree that there should be more resources pumped into this area. I have had both a lumpectomy and a double mastectomy. Both times I found the lump myself. Because I have had a double mastectomy, I have had no scans since my last surgery - again a regular ultra sound, would give me some  reassurance. I was first diagnosed 14 years ago and have been through what you are going through - I suspect that most of us here have.  I have availed of all of the above services and more, in an effort to get myself out of that "hole". By helping yourself in some of these ways, you will find that you will not only make new friends, but you will help others along the way and this satisfaction should help to lift your mood.

    The only answer I have personally found to helping with the emotional turmoil caused by Tamoxifen, is unfortunately, medication. I eventually resorted to Venlafaxine and it made a tremendous improvement. 

    I hope that you will soon feel more positive about your situation and can start to move forward - life is too short for what ifs!.

    Kind regards,

    Jolamine xx

    .

  • Hey everyone since chatting on here I have joined a gym and volunteered to work for a cancer charity that helps people to an from hospital for there treatment I’m in the process of DBS checks etc but they hope to have me start in December and it’s all thanks to reading all your stories and knowing I’m not in this alone it’s way out my comfort zone but I’m gona give it a go good luck guys sending big hugs and thank you for sharing xxx

    jen

  • Offline in reply to Jenstew Unpublished Reply

    Oh such good luck, so encouraging and lovely hearing your message. Just remember to perhaps do your own research and not be afraid to pin these experts to the ground. They will wriggle and tell you anything

  • Hi Jen,

    That's fantastic - well done! The service that you will offer is invaluable for those who have to attend hospitals regularly. This is also a great way to meet other people, as you will not only meet the patients, but also the other volunteer drivers, who are waiting to pick up their charges after treatment. I sincerely hope that this goes well for you when you start in November.

    Please stay in touch and let us know how you get on.

    Kind regards,

    Jolamine xx

Reply
  • Hi Jen,

    That's fantastic - well done! The service that you will offer is invaluable for those who have to attend hospitals regularly. This is also a great way to meet other people, as you will not only meet the patients, but also the other volunteer drivers, who are waiting to pick up their charges after treatment. I sincerely hope that this goes well for you when you start in November.

    Please stay in touch and let us know how you get on.

    Kind regards,

    Jolamine xx

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