Hello Joy,
I know that at this moment in time words just aren’t enough but I am so sorry to hear about your Mum. I understand what you mean about the reality of it all as when you're caring for someone, you don’t really have time to think about what's going on, you just do everything you can to make what time they have left more comfortable. But then when the time comes for them to leave and you’ve struggled through the funeral, life just seems so empty and you have the time to look back on everything that’s happened and its only then that it all sinks in. My Mum passed on June 28thlast year and most days I still find myself asking ‘why’. Why my Mum. Do you have a good supportive family? All the people on this site are marvelous, they always have the time to listen. Although I don’t always post on here, I find myself reading all the other posts every day now, and it really helps me. I only wish I had come on here last year when I was so desperate to talk to someone but didn’t know who to turn to. My thoughts are with you, please come back here and talk, I know its very early days for you, but it really does help to share how you are feeling, especially with others who, like yourself, have gone through so much. Take care. Jayne xxx
Good Morning Susan,
How are you today? Yes it does sound that your Mum was in some way directing you to this site. It’s strange how things happen sometimes isn’t it. I originally came on here way back in August 2005 when Mum was diagnosed. I came on to see if I could find out more about CML, but then when Mum started getting little things wrong with her (Feb 2006), I’m ashamed to say that I forgot all about the site because I was busy taking her to appointments and rushing her down the hospital to get IV antibiotics. I had signed up for the newsletter by email, and it was when I got one just recently that I thought I would buy a Mcmillan 2007 diary, and it went on from there really. It has helped so much. I was supposed to have gone for counseling last year. One of the counselors from the hospice phoned me up totally out of the blue to see how I was coping. Although I think my doctor had something to do with it because I had gone to him for something else and when he asked how I was, I just broke down. So I think he must have phoned them, he’s the best doctor anyone could wish for, so understanding. He looked after my Mum. He even used to turn up at the hospital and the hospice to see her. He genuinely does care, what I call ‘a real doctor’. I never did go to see the counselor because when I phoned up to cancel the appointment, we ended up talking on the phone for nearly an hour and I felt better afterwards. I feel that everyone on this site has helped me so much, and in a way, to me, you are all my counselors….. so thank you everyone x.
Well, I guess everyone has rushed off to work now. I feel so useless not having a job anymore but hopefully something will come along soon. It’s funny because before Mum was diagnosed I used to say to my husband “can we afford for me to pack up work or at least go part time”. He used to say “no definitely not”. But now look how things turned out! I’m waffling on about nothing in particular again, so better go. Take care. Love Jayne xxx
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