Jump to content

palm

Members
  • Posts

    7
  • Joined

  • Last visited

Posts posted by palm

  1. Rochelle: As for all of us the beginning of this journey is the most difficult. Two words helped me through this phase and is still helping me after 15 months, LET GOD. I couldn't do it without the prayers of my family and friends and the belief that God has a plan for me that I need to accept.

  2. Just got results of CT scans, MRI and PET yesterday, and not so good news. Several small spots on left lung, spine, ribs and a large one on right femur. I will be starting a clinical trial tomorrow with epirubican and irinotecan. Has anyone ever used these and if so with what results.

    I was diagnosed with sclc limited August 04

    Had cistplatin and VP16 for four rounds and radiation to left lung, successfully resolved lung tumor at that time, but now it is back.

    I am desperate for an answer.

  3. I finished 15 days of PCI two months ag, and I think the side effects are worse now than they were 2 months ago. Extreme fatigue, nausea. Zofran is good. My Radiology/oncologist said there is no reason for me to be nauseated at this point, and I should be getting over the fatigue. However, my oncology nurse said sometimes these symptoms can last up to a year.

    My husband has been very supportive until he hears these doctors say I shouldn't be having these problems. He tends to think it's psychological and even asked the doctor if it could be. Doctor said it could be. Just what I need on top of feeling so lousy. A husband & doctor that think I'm goofy besides.

    When I hear these other postings saying they are feeling the same way, it makes me think maybe I am not crazy, although I am sorry for anyone else to be going through the same. I may hve to start chemo again next week, and can hardly tolerate the idea feeling the way I do with this other stuff. Sorry to sound so dismal. I have been very optimistic until now.

×
×
  • Create New...

Important Information

By using this site, you agree to our Terms of Use.