mmead534

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  • June 21, 2012 at 8:08 pm in reply to: Im new here afrom NY and a caretaker for a cholangiocarcenoma patient. #60055
    mmead534
    Spectator

    Thank you Gavin, Im kind of numb right now but its good to know I can vent here. My friends and family have been great but I hate to be a burden.

    The worst thing about this disease is watching him so sad and the next worst thing is watching m sons suffer wataching him. They are both young men but I hate to see them see him like this. Just hoping for some more time.
    He goes to the onc on Monday.

    June 21, 2012 at 7:26 pm in reply to: Im new here afrom NY and a caretaker for a cholangiocarcenoma patient. #60053
    mmead534
    Spectator

    oops I didnt read your post carefully. Sorry for your loss. I know what you mean about being addicted to a group. I lost twin babies 22 years ago and I continued participating in the group at the hosptial for about 10 years and I still subscribe to the newsletter PS Support and donate yearly. It keeps my babies alive inside of me.

    June 21, 2012 at 7:23 pm in reply to: Im new here afrom NY and a caretaker for a cholangiocarcenoma patient. #60052
    mmead534
    Spectator

    Do you have cancer or did you loose a family member. I read that the contents of my posts should be positive so here goes. Its been a little over a year and he is still living home with me and going for treatment :)

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