Feeling lost

Hi, Mt name is Lesley and I am just about to have the last of 6 treatments of chemo.  I seem to have suffered with lots of the side effects from constipation, watery eyes to numb fingers and toes and everything in between.  Some days I have wanted to run away and hide in fear of what I will get next.  A little history,  I had breast cancer back in 1998 and following a mastectomy had both chemo and radiotherapy.  I took tamoxifen for 5 years and was then told to go and enjoy my life.  Well I got almost 20 years, but in April 2016 I began to get a tickly cough that I just couldn't get rid of. A visit to the gp who insisted at first it was hay fever and then asthma meant that I wasted 6 months before a referral to a respiratory specialist, which took another 2 months before I could get an appointment, following a ct scan cancer cells were found in my lung and unfortunately throughout my bones. I'm a glass half full sort of person, but cannot get my head around what happens next, to see palliative care on my file scares me and I don't know what to do. I haven't spoken to anyone although I keep being asked if I have spoken to McMillan nurses

  • Hi there Lesley

    My name is Lynne and i, like you, have a bit of a battle going on at the moment. I was so upset to read that you had been clear for so long, and now it's kicked off again. And I'm sorry to read that it took so long for the docs to diagnose your cancer, as we know every moment counts. I'm glad to know you're a glass half full kinda gal, I am too, and it really helps to retain that if you can. That as well as a sense of humour is crucial and to give and receive love is a great boost to your immune system. Please forgive me if I'm telling you things you already know, I just want you to know that I'm thinking of you and I send you my love and best wishes.

    Love LynneF X