Guest guest Posted January 10, 2008 Report Share Posted January 10, 2008 I am very new to this, and I am reading all the posts, and doing as much research as I can. The majority of my posts will probably be questions instead of reponses to posts. But I want you all to know whether you are the one with the disease or the caregiver I'll keep you in my thoughts and prayers. As I told you in my first post, my hubby refuses to talk to me about all of this, and he gets angry if I mention anything about it to him. Well, I figured out, I can email stuff to him, and it doesn't bother him. Next week after his ultrasound, I will send him the link to this group. But for now, I am emailing him something about HCV everyday. Yesterday, I emailed him some information you all posted about supplements and iron...and diet. Well, when he came in for lunch yesterday, before he took his vitamins, he came to me and told me " look, there is no iron in these vitamins " . And then he asked me if I knew about one of the other ingredients that was listed. My only response was " That's good about the iron, and I know what all else is listed because I've already checked the label " I didn't say anything else, and just went about my business. But I feel like we took a step forward in the communication area. Today, I am going to send him the list of " Foods that make the liver happy " that sent to me. And I am going to send him the link to article that starts off " Being Detected With HCV Is NOT a Death Sentence " I know now for sure, he is reading what I sent, and he is not getting upset with me for sending them to him. I'm sure it's going to be up and down until we know exactly where he stands with this, but I know we'll have the support we need from this group. Thanks again for being here. Quote Link to comment Share on other sites More sharing options...
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