ME and breast cancer

I have lived with ME for nearly fourteen years.  Most of the time I have it under control with cognitive behavioural therapy.  Last month I was diagnosed with breast cancer and have just had my first round of chemotherapy with seven more to go over the course of sixteen weeks.  Following that I have to have surgery followed by radiotherapy.   I will not be finished with treatment until October/November.   I am 69 years old and this last week have experienced fatigue like never before.  I was wondering if anyone else has been in my situation and how they coped.

  • Hello pPicasso14

    I'm sorry to hear about your recent diagnosis and that you're also living with a long-term health condition. Undoubtedly this will have made things difficult for you. 

    It's good to hear that you've been able to use CBT techniques successfully to manage some of the symptoms of your ME. Whilst the chemo will certainly have an impact on your physical health, we know that having a positive mindset can really help with managing those side effects so I'd encourage you to continue using those techniques. 

    Do speak to your breast care team and let them know about how you're feeling and I'd also encourage you to get in touch with your local Maggie's centre. Many of them are running online groups and classes and you may find it helpful to join a support group or relaxation class. 

    If you'd like to chat things through with one of our nurses at any point you're most welcome to give them a call. I'm sure they will be happy to offer some support. They're available Monday to Friday from 9 am to 5 pm on 0808 800 4040. 

    I hope this helps and that things improve for you. 

    Best wishes, 
    Jenn
    Cancer Chat moderator 

  • Thank you for the reply.  CBT has been and will be part of my life.   I must admit it has helped over the past few weeks considerably.  I had my second round yesterday and, although exhausted from the experience, it was not as bad as the first.  I think my body went into shock the first time.  Still waiting for the side effects to kick in.  I have a good circle of support from friends and family and, at the moment, not ready to join a group but will definitely keep it in mind as I feel probably, in the future, I will feel the need.  
     

    Thank you for the information 

     

  • Hi,

    I'm really sorry to hear about your diagnosis. I've had M.E since I was 14 , I'm now 52 so I've lived with it most of my life. Several years ago I had double pneumonia and my M.E worsened to the point that I was classed as disabled and had to give up working.

    Last September I was diagnosed with stage 4 inflammatory breast cancer. I've got one session of chemo left (out of 8) after which I'll be on target drugs for the rest of my life. During my chemotherapy I've had covid and neutropenic sepsis and I'm currently battling anemia and pneumonia. 

    It's certainly not an easy road to go down but the thing that keeps me going is I'll have more time with my family.

    Unfortunately I can't suggest a miracle solution it's tough and likely to get tougher. You've been given an end date so focus on that. Listen to your body. If you're not up to doing something don't do it.

    Over the years I've learned to be kind to myself. I have days when I can't get out of bed. Other days I can make it to the sofa. I rarely get dressed as it exhausts me and I no longer do anything in or around the house. I sleep when I need to which is often a couple of hours during the day before an early night. I also eat healthily to provide my body with good nutrition.

    Good luck with your treatment and focus on how different things will be at the end of it.

    Take care 

    Barb

     

     

     

  • Hi

    thank you so much for your kind thoughts.   But, compared to you, my situation is quite mild.   You have really been pulled through the mill and my thoughts and wishes are with you.   Yes, there have been days for me when I don't want to get up but I do still have that spark to do it even if it means just sitting in the sofa.  My cancer is stage one so, to all intents and purposes, curable and, yes, I have been given a date that I can focus on.   My husband, whose own health is far from good, is doing a wonderful job of looking after me at present.  My children who live in Australia and America Facetime every day so we are close.  
     

    You are right to be kind to yourself you deserve it.  I am coping with the side effects although not very pleasant.  Just starting to lose my hair.  I thought I would be distraught but, quite the opposite, I find it amusing that my short blonde curly hair is thinning by the day and I will be bald.  I think if I had been 20 or thirty years younger it would have affected me more but, at my age, it just goes along with the saggy boobs and everything facing south so I go with it.  I am satisfied that the treatment I am getting will make me better although the journey through it is, and will continue to be, awful.

     

    Thank you for your reply and I hope your journey along this awful road will improve for you at some stage.  Think positive thoughts, rest and eat as well as you can but, most of all, take care. X