sw55

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Viewing 15 posts - 16 through 30 (of 39 total)
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  • in reply to: Update on Lauren #72236
    sw55
    Member

    Pam,

    My heart is also breaking for you and your family. My thoughts and prayers are with you at this difficult time.

    in reply to: Please, I need your input #72354
    sw55
    Member

    My oncologist at MDA did mention clinical trials at my first appointment, but it was presented as something we might try if standard treatment did not work. I would consider a clinical trial.

    in reply to: Having procedure today, 5/20 #72426
    sw55
    Member

    So glad you were able to get the stent!

    in reply to: Need some help with suggestions #72437
    sw55
    Member

    Cathy,

    I’m sorry I can’t really help but you said you changed steroids. Could it be a reaction to the steroids?

    in reply to: Update on Lauren #72141
    sw55
    Member

    I am so glad Lauren is doing better. You are constantly in my thoughts and prayers.

    in reply to: Chronic Hives #71923
    sw55
    Member

    I hope the new doctor solves the problem and you are feeling better soon!

    in reply to: Clear scan #72064
    sw55
    Member

    Wonderful news!!!

    in reply to: Lauren’s 2nd Surgery News #71984
    sw55
    Member

    Praying for Lauren.

    in reply to: Lauren’s 2nd Surgery News #72017
    sw55
    Member

    Pam,

    So happy for you and Lauren. I hope you can get some rest now.

    in reply to: MRI abdomen/CT chest scheduled for tomorrow #71952
    sw55
    Member

    Good luck Randi!

    in reply to: Lauren’s Surgery #70263
    sw55
    Member

    Pam,

    Lots of prayers coming your way and Happy Birthday!

    in reply to: I might be getting a new liver…and SOON! #71786
    sw55
    Member

    Wonderful news Tiffany! I am so happy for you and your family.

    in reply to: Starting SBRT Thursday, 5/2 #71407
    sw55
    Member

    Mary,

    In response to your question about stents, I have had a plastic stent in my bile duct since September 2011 that I have replaced every 2-3 months. They put you to sleep and you will never know they did anything.

    Good luck with your treatments. Sending positive thoughts that you will be able to finish!

    in reply to: Gemzar/Xeloda #71178
    sw55
    Member

    Kris,

    Fortunately I have great insurance at work- Blue Cross PPO and my co-pay was only $40 but that is good to know. How long were you on Xeloda before you started having hand and foot syndrome?

    in reply to: clean scan #71095
    sw55
    Member

    Fabulous news Susie. Congratulations!!

Viewing 15 posts - 16 through 30 (of 39 total)