tanoland

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Viewing 15 posts - 16 through 30 (of 97 total)
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  • in reply to: A request from a patient #33798
    tanoland
    Member

    No reason to sugar coat it…not for the patient or the caregiver. When my sister got diagnosed…the first thing I did was get on the computer for research. This is one of the first websites I went to and … yes…it was a slap in the face to hear how bad this cancer really is. But it also got my attention that you have to fight with everything you have from the first second you are diagnosed. I think calling it what it is makes you fight even harder. It has taken the people we love the most away from us so there are no other words for it than horrific, horrendous, awful, beast…whatever. Actually I have a few words for it..but they would not be allowed on here.

    I’m sorry you are having a difficult time reading this. My sister could not have read anything on this website. It would have hurt her too much. So I did it for her. Sometimes that’s best.

    in reply to: CCF Wristbands #31520
    tanoland
    Member

    Hi Julia…I’m doing o.k. Bad time of year. This is the time when my sister really went downhill last year. I’m trying to stay positive and happy like she would have wanted me to. Thanks for checking in on me. I’m checking this website every day…

    in reply to: Volunteers, we would love to hear from you #32974
    tanoland
    Member

    I have submitted myself to volunteer for anything that I can. I would love to do something in memory of my sister.

    in reply to: Can’t imagine the end w/my Sister #33307
    tanoland
    Member

    Wow Jane…I felt like I was reading something I would have written when I read yours. My sister was 42 with 2 children. And I felt exactly what you just described.

    in reply to: Can’t imagine the end w/my Sister #33304
    tanoland
    Member

    I went through the same thing with my sister 10 months ago. You will find strength and wisdom you never knew you had. I will pray for your family.

    in reply to: The journey starts #33025
    tanoland
    Member

    tomf you should start a blog. It’s very interesting reading about your experience.

    in reply to: Hmm, seemed like just another Monday #32216
    tanoland
    Member

    I come here numerous times every day checking in on everyone and my sister has been gone 9 months:(

    in reply to: Lisa #32072
    tanoland
    Member

    It’s so good to hear you are out of the hospital. Just keep getting better:)

    in reply to: Cholangiocarcinoma Awareness Month #31977
    tanoland
    Member

    I voted for January…the month this disease took my sister from me.

    in reply to: Johnny Ur #32055
    tanoland
    Member

    His blog is on the Blog section on this website.

    in reply to: Things happening quickly #31899
    tanoland
    Member

    My sister’s had spread to her lungs at the end…once the chemo had quit working. I don’t know why once it spreads they decide to quit treating. But that’s what they did with her. And it’s scary how fast this cancer spreads.

    in reply to: It’s not over until the fat man sings, right? #31709
    tanoland
    Member

    Trust me…you will never know what to do…you just do it. You sound just like me when this all started for my sister. The guilt is overwhelming…but I think your family will understand if you need to be with your mom. I have a husband and three children and when my sister was at the end…I spent 14 days and nights with her until it was over and didn’t see them at all. You will find the answers as it goes along. Good luck.

    in reply to: CCF Wristbands #31519
    tanoland
    Member

    I feel the same way…I feel proud to wear my wristband…and sad. This wristband never, ever leaves my wrist. I feel closer to my sister …which I know is odd…but that’s o.k.

    tanoland
    Member

    Your story sounds so familiar to my sister’s. I swear she suffered no matter how much medication we had.

    in reply to: New to this…. #30892
    tanoland
    Member

    Hey, I am from Kansas too. My sister had her doctor at K.U. Dr. Stephen Williamson. She also had her treatment at the Cancer Center there. You will always feel this way with this disease. I’m not sure they know anymore than they are telling you. I always felt that way. I wanted so much more information but it was never there.

    I’m sorry you and your sisters are dealing with this. I’m sorry for everyone who has to deal with this awful disease:(

    Take care.

Viewing 15 posts - 16 through 30 (of 97 total)