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Friday, November 04, 2005 

News from Lake Michigan

It's been 68 days since we flew home and living day to day with0ut plans for the next has transformed into a life of less conscious uncertainty. I have spent the past two nights in Chicago where I spoke on peer-to-peer file sharing (music sharing online) and the law. The technology is interesting, the economics and the law part, but the impact on people is what I notice the most, since I talk to lots of customers who have been sued by the music and film industries.

Since returning to the office, I've been doing my own work and that of pretty much two others, which takes its toll in time, frustration and timeliness. It doesn't seem to be something that will change soon.

John let his allergy medicine lapse, which led to a few worrisome days of symptoms that have dual meaning. He is back on it now and I hope will be better. Our coexisting with a 20 something has settled into a comfortable enough state, with him waking at noon, going out around dinner and returning after midnight. When our times overlap, it is nice, as we do a few times a week when what he needs is a good dinner or to have his friends over.

Debbie's dogs were away for the past week at "'Camp Rona", Peggy and Rona's menagerie. They had gotten a kitten and Sara, who is blind, but still playful, found a new friend in it.

It's early now, even for Chicago, and time to return to all the things that make work a four letter word.

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About me

  • I'm Randy Cadenhead
  • From Atlanta, Georgia
  • My son John was diagnosed in November of 2004 with Acute Myelogenous Leukemia (AML). Since then, he underwent three rounds of chemotherapy and received a bone marrow transplant in Seattle. This site is about his experience, as seen through his father's eyes. Links to John's website and to his own live journal are below.
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