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FormerMember
FormerMember
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Whether you’re here to talk to others, join a group, ask questions or just listen, everyone is here to offer emotional and practical support to help you with your cancer journey.

We know it can sometimes be confusing when you first arrive, with lots of forums and groups to choose from. So this thread is to welcome you, make friends and help you find your way around the site. Whether you are a patient, family member, friend or a carer, feel free to post any thoughts or questions here and other Share users will be happy to help you navigate around the site and find what you are looking for.

  • FormerMember
    FormerMember
    Hi Mackem,There is also a group for non hodgkins if that is the type of lymphoma you have.Hope everything goes ok with the chemo.Joan x
  • FormerMember
    FormerMember
    Thanks Joan

    I have T-cell NHL. Thanks to everyone for their kind words. Will let you know how I get on next week. Doing fine physically but not so great otherwise. Not looking forward to telling anyone so just havent so far except my partner. Not good at that sort of thing at the best of times.

  • FormerMember
    FormerMember
    I had follicular NHL, dont Know anything about T-cell,there may be some one in the group who does.
  • FormerMember
    FormerMember
    Hello everyone

    I have been logging onto this site and reading the heartbreaking posts for a while, but I have only just plucked up the courage to register and post. I have lost several people I cared about to this horrible disease, but in particular my mum to bile duct cancer and my dad to bladder cancer within 14 months of each other in 2005 and 2007. They were 71 and (just) 72 respectively but they were in perfect health until diagnosis and both had so much to live for. My family think I should be 'moving on' by now, but I still miss them so much every single day. What I wouldn't I give to be able to pick up the phone for a chat as I did most days.
  • FormerMember
    FormerMember
    Wendy,

    Sorry to meet you here but there are so many people that struggle to come to terms with what has happened.
    I notice that your family say you should 'move on' - er I find that particular phrase offensive and somehow lays 'blame' at your feet.

    What you will find is, that sooner or later, and it is a very individual thing, your life moves on and takes you with it. Your parents live on in your genes, your heart and your mind. Cherish the memories and talk about them as much as you want.

    Mick
    xx
  • FormerMember
    FormerMember
    Hi Mick

    Just read your profile. I just want to say hi and that I noticed it was your wifes birthday yesterday and feel as though I just want to acknowledge this and I hope you spent the day well.

    xxxxxxx Suzie3 xxxxxxxxxxxxxxxxx
  • FormerMember
    FormerMember

    Hi Everyone. I am a newbie. I am not unfortunately new to cancer as I had BC and mastectomy 5 years ago when i was 28. I have just this week started Zometa due to dodgy looking bone scan/MRI. My partner and father of my lovely 6 year old upped and left in January and I am only just getting used to the fact that he has gone and is not coming back - and now i have the awful big "C" hanging over my head again. This all seems a bit much for a 34 year old and I guess I just want to talk to some other people who have gone through the same thing. The worst thing was that I sailed through chemo - never a bad day - but this ZOmeta has made me so so ill with shakes, fever, aches, sickness etc. feeling very sorry for myself at the moment....

    Sam xx

  • FormerMember
    FormerMember

    Hello to all,

    I have just joined the site after finding out my mum has cancer for the fourth time in nine years. It started with breast cancer all those years ago, bowel cancer then followed with secondaries in the liver. What we face now is secondary bowel cancer again this time on her right lung and in the lymph node. As far as we can tell they have caught it early but mum does not want any more surgery and we have been told that it probably won't be an option anyway. They have said there is no hurry to start chemo but she will be having capecitabine and Ironotecan if she agrees after reading about the side effects. I know it is early days, they found it very quickly, but I also know that we are not talking about a cure only treatment. I believe this is the beginning of the end. Any comments would be wellcome but I would like to know what we face and if anyone would know roughly how long we can expect to have her for.

  • FormerMember
    FormerMember

    Hi Wendywonder,

    So sorry to hear about both your mum and dad. I can understand that you still miss them, and want to talk about it. You may find the best place to post i s the "Coping with Loss Board" which you will find over to the top left of the page. Most people on there have lost someone to cancer and can readily sympathize with you, and I am sure you will find many to talk to.

    Welcome to the site, Sending you big hugs x x HarryB x

  • FormerMember
    FormerMember

    Hi Sammyanna & mummy's girl and welcome to the site, but sorry for the reasons you need to be here.

    Sammy, if you go to Tags on let hand side of page you will see Breast. If you click on there you will find other threads dealing with breast cancer and you will be able to contact others that are facing this cancer too. You can request friends, or add replies to join in the discussions.

    Mummy'sgirl, Having cancer for the 4th time, does sound terrible, but don't give up hope. Your mum is obviously a fighter to have come through what she has done so far. There are others on here who have been fighting this disease a very long time, so I dont think anyone can say how long you will have your mum with you, because everyone is so individual.

    You will find there are great people on here who will encourage and support you through your journeys, so please keep posting, either on this thread, another one you like or by joining one of the appropriate groups. Love & hugs to all x x x
    HarryB