Guest guest Posted September 7, 2010 Report Share Posted September 7, 2010 Thank you Sue, for your description of your experience and your compliment. We each have our own style of writing which is unique to each of us. People recognize you by the way you express yourself and you have a very warm way of comforting people who may be experiencing some difficulties in their lives. Your choice of words are very complimentary and personal to the person your message is directed to and you should know that your expressions are a great consolation to our friends in distress. I'm sure they will appreciate reading about how you lived through those days (horse & buggy days). I know that not all trials are the same as they progress in knowledge of how the patients react to assimilating the drugs. I know that not all of my trials were exactly the same, I was describing only 1. The first time I went to MDACC they kept me 16 days straight running tests and seeing how I would react. Jimmy had to go to classes on how to give me the INF and how to change the dressings on my central venous catheter. It was nerve wracking for him and he shook so much he would drop things that had to be sterile and we would have to open a new pack and start all over. Your spouse is just as involved in all of this, it's like they are sharing your disease like everything else in your marriage. I can't thank my Jimmy enough for his love and patience to drive me back and forth to Houston, even when he is sick himself. I can't imagine how it is for parents and their children. So to everyone, I would ask that you share your story with us and give us a glimpse as to how it was with you. It may be about how you traveled, how you found your doctor, how you reacted to the drug or how well you accepted it, someone you met that really impressed you, did you have a bad experience with your luggage or at the hotel? Carpe diem, Lottie Duthu Quote Link to comment Share on other sites More sharing options...
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