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  • Bibby's blog
    Not the greatest night I've ever had
    What a night.....just been at Frankie's beck and call all night. These steroids just make him a nightmare. He gets so irritable and demanding. Went to bed very early (7pm)....got woken up by him demanding food at about 12. Did that, came on What Now. Then he had spilt Ribena all over his/our bed so at 3am I'm changing a King Size bedsheet on my own. Not an easy task and now my mattrress is stained with Ribena......grrrrr! Went back to bed and of course he was up with the larks. 6am. Bouncing off...
    Former Member
  • notsineadoconnor's blog
    update: things are better than I thought!
    Thanks to everyone who replied to my last blog, no one understands what this like better than the wonderful people on this site. Saw the oncologist last Monday, the CT scan was clear!! However, ca125 is still up. Am having another scan , blood test and appointment on 23rd November.Am really happy as I had prepared myself for more chemo straight away.Was told the cancer is back but on a microscopic level. I will not be treated until something shows on scan.Still feeling very well. Julie
    Former Member
  • suzy oliver's blog
    Herceptin side-effects
    Hi I'm curious to know if anyone is experiencing side-effects from herceptin? I've been having it 3 weekly for the last 9 months, the first 6 were given with chemo, and am to continue with it for another 7 months, so in effect a year by itself. I have it on a Friday and now by the Monday I am achy - legs the worst - and sooo tired. Not as bad as chemo but I am having to take to bed and feel like this for a good week now, a little bit longer with each one. My oncologist tells me this is ok, I...
    Former Member
  • dotty57's blog
    wating for results
    The waiting game is the worst it feels like forever, the lung biopsy result was ok but they are not sure the tissue came from the right place my oncologist is asking for removal of tissue another waiting game it just goes on and on feel angry that a friend has had an nhs tummy tuck when we have to wait lol dt x
    Former Member
  • KarenTx2's blog
    Mum is very down !!
    Mum had her appointment after her op .. Good news the cancer hadnt spread to the lymphnodes as suspected . They are confident they have got all the tumour out but she still needs Radio and Chemo therapy.. She is very upset about the possibilty of losing her hair ... She is 55 years and still has long blond hair with sprinkle of grey .. She is worried it will grow back grey. She is single and has always been attractive to men and is worried she will now be on her own forever. She is panicking...
    Former Member
  • carolannt's blog
    mum it's over
    just got back from the hospital , mum passed about 5 pm . thanks for all your support love carol xx
    Former Member
  • carolannt's blog
    mum it's over
    just got back from the hospital , mum passed about 5 pm . thanks for all your support love carol xx
    Former Member
  • Sam82's blog
    Life is just not fair
    On the 22nd July my world collapsed around me when my dad was diagnosed with lung cancer which has already spread to his brain, he is 67 and he is my whole world. Dad is going through a divorce at the moment after parting from my Mam last August so he has had the worst year ever. Dad had his first chemo session yesterday (14th August) which was Carboplatin and Gemicitabine, today he is a little tired but no other side effects, next session is Friday. Dad is a very very heavy smoker but he took...
    Former Member
  • 51merc's blog
    What Happens Next??
    Hi I met with the consultant on Tuesday who has told me I need to have a cone biopsy and then lymph node removal afterwards to remove the glandular cancer cells in my cervix. (stage 1B) What I don't know is how do you cope with waiting for the results, I had to wait six weeks for the results from my loop biopsy and as I have given up smoking, not sure how I will cope with the wait. Any idea's? Also how can the doctors say they are confident this is all the treatment I will need?, not even got...
    Former Member
  • jo armitage's blog
    Another Chapter !!!
    Hi all, Just finished my 6 months chemo regime. Feel great. No more sore,burnt feet and numb fingers and all other side effects that go with it. For those of you still on it, just keep going, it's hard, but when you get to the end it is a great sense of relief and achievement. After 18 months of gruelling treatment, I have now got to the end with NED for now, and so glad to be still around. My consultant and oncologist were wonderful throughout. Don't think I could have got better treatment...
    Former Member
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