NOW (2016) –
This site is less of a blog (which requires the kind of regular care-and-feeding that I just can’t pull off) than a place for me to share drawings and music, make occasional observations, and in general, get some of the thoughts that are rolling around in my head out into the world-at-large.
This blog was started back in 2008. The family was spending a fair amount of time at the Cleveland Clinic, trying to learn what we could about Lisa’s seizures. Now (looking back from 2015), all of that’s behind us, but I’m leaving those posts up both as a record of our own history and as a possible source of information and support for other families who might be going through similar struggles – health, diagnosis, seizures, tension, fear – all of the things that come with having a child with medical issues.