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  • 5 Apr 2011 - 18:10
    <none>'s picture
    0 comment(s)
  • 4 Apr 2011 - 18:27
    Rachel C's picture

    Just wondering if anyone else has those down days. I finished treatment in November last year, 2010 and returned to work in Feb 2011.Today was just one of those days, where everything seemed to go wrong, or maybe I was just more vulnerable today.It is strange returning to the same things but I feel a shift in myself, a restlessness.
    Perhaps because I experienced something so confronting I feel like everything needs to change. I find myself assessing everything from friends to work to family.
    I suppose I just want things to go back to how they were.
    Does anyone else feel like that?

    11 comment(s)
  • 3 Apr 2011 - 16:58
    junstel88's picture

    “IMPACT OF BREAST CANCER DIAGNOSIS TO THE OVERSEAS TRAINED DOCTOR'S WHOLE FAMILY”

    PERMANENT RESIDENCY VISA OF OUR FAMILY REFUSED BY AUSTRALIAN IMMIGRATION BECAUSE OF BREAST CANCER

    Hi All,

    Good day! I’m Dr Cesar. My wife Mary (41 y/o) was diagnosed with breast cancer with brain and lung metastasis. We have two lovely daughters ages 13 & 10 y/o. I hope you don’t mind if I’m going to share our family’s experience and “adventure” here “Down-Under” Australia since 2005.

    9 comment(s)
  • 2 Apr 2011 - 01:34
    SILLY's picture

    In reply to a quote about fear being the strongest human emotion(posted by Jules2),I think it could be true.It brings to mind fears I have-how I look to strangers after cancer treatment,fear of not outliving my husband and leaving him alone,of not seeing my grandchildren grow up and of not being ready when the end is near ,possible recurrence ,metastises, pain.....

    Of course ,illness aside there are many common fears we humans have- no need to give examples.

    I try not to dwell on these fears but they are there. They pop up from time to time.

    0 comment(s)
  • 31 Mar 2011 - 18:07
    Rachel C's picture

    Hi I noticed that someone has mentioned, sore feet. I had sore feet also after the chemo. The doctor said it is called peripheral neuropathy and to take vitamin B6 and have foot massages. This seems to have helped a bit.

    1 comment(s)
  • 30 Mar 2011 - 17:10
    maddie86's picture

    im so nervous its my boyfriends operation finally to remove his tumor from his bowel on monday.. he'l be in hospital for apporx ten days they said..
    then after that two weeks after he'l have his lungs operated on and liver to remove spots and nodules.. its been nearly a year now since he's been diagnosed and i just cant believe its come around this quick! im nervous and excited, feeling a lot of emotions all at once! has anyone had bowel resectioning before?? they said he should be right because he's young and will recover quickly..

    6 comment(s)
  • 28 Mar 2011 - 16:07
    BJS's picture

    I've been reading lots of stories about the different kinds of diets cancer patients are on. When my husband first started chemo we were giving him lots of small meals high in protien, as time progressed & he started to get his appetite back we slipped back to our normal diet of 3 meals a day. He has always managed to maintained the same weight as he was before he got sick but now I'm getting worried that I'm not doing enough diet wise to help him get the best results.

    3 comment(s)
  • 28 Mar 2011 - 15:58
    VLASTA's picture

    Hi , I'm 45 year old and on 18/02/2011 I've got diagnosed with an endometrial carcinoma stage 2 and on 04/03/11 I already had a total hysterectomy where also 20 lymph nodes were taken out and one of them was infected which puts me one more stage further, I think. At the moment I'm still recovering from the operation, waiting for my radiotherapy ..... My Dr. told me that I might be offered a trial combination of radio-chemotherapy, does anyone out there has more experience which therapy is more useful..... Thank you

    Vlasta

    6 comment(s)
  • 27 Mar 2011 - 02:54
    BJS's picture

    I'm new to this & I'm just starting to reach out for help. I will be phoning the Cancer help line on Monday to see what they can tell me. My husband has cancer of the oesophagus & after nearly six months of Chemo we've just received his results which were not good. I feel his Oncologist has abandoned us saying there are no secondary treatments for oesophagus cancer. The oncologist said he will moniter my husband over the next few months & also make inquiries to see if he can get him into a clinical trial. Is there anyone out there who knows about cancer of the oesophagus?

    5 comment(s)
  • 27 Mar 2011 - 01:18
    SILLY's picture

    I want to praise the Cancer Council of QLD as I had help from the counselling service. Prior to that when I rang to enquire about it I was on the phone for over an hour and a half. It was good to be able to get it all out -fears, questions ,doubts etc.talking at length to an understanding person and having my feelings validated.

    Friends and family try to help and many did, but sometimes their comments show that they really do not understand.

    4 comment(s)

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