Guest guest Posted November 7, 2009 Report Share Posted November 7, 2009 Dear Jo Ann, Yes, knitted caps do count. Jo Ann, you would have done the same thing had you been in our positions at the time. There was nothing else, so what were we to do? Just keep us updated on how you are doing, we all want what is best for everyone, including your other health concerns that may hinder your current CML treatment. The questions keep our doctors on their toes, as China said, so we all have something invested in this journey - our lives and the pursuit of happiness like the rest of the population. Like Ceil is experiencing, we all have bumps in the road, but we fight on, using the tools (knowledge) we have gotten from our CML community. I knew absolutely nothing about this disease until I joined a support group. My doctor hated to see me coming through the French doors because I always had a stack of information I had downloaded from my computer. He sorted through them and threw most in file 13, but that is how I learned what I wanted to know about this disease. True, it is not a cakewalk, but there are worse things than CML, I have convinced myself of that. You and Bobby should get together on the caps. LOL She crochets them for cancer patients who have lost their hair. This lady has traveled more than anyone I know to get CML's latest treatments and if I am not mistaken, has tried them all. I don't think she has gone to Mexico to try the coffee enemas just yet. LOL I know Bob will have something to say about that. What about it Bob????? Hands & hearts and have a fun weekend, Lottie Duthu Quote Link to comment Share on other sites More sharing options...
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