My life changed dramatically when I found out I had a rare congenital brain disease, characterized by a cerebral arteriovenous malformation. This went unknown until it hemorrhaged in 2012; I was 24 years old and in the first semester of grad school. Luckily, I survived and am now writing a book about it – this blog chronicles that journey.

In 2020, I have decided to pivot a little, making Nomadic Caffeine an interactive space for sharing & support. Among our community are stories from survivors – students, caretakers, mothers, professionals, wives, medical staff, husbands – regular folk like you and I who experienced the unthinkable. Take a look around for a moment; if you have the time, sit, sip and scroll.

For the writer’s who have stumbled on Nomadic Caffeine - don’t worry, I’ll still be popping in from time to time to talk about my book writing progress; you’re grandfathered in to the action. Ha.

Lastly: I was born and raised in the middle bumble fu*k Iowa, spent some time in the Minnie Apple and currently devote my rainy days to Seattle, Washington.  Writing has always been something I have enjoyed – advocating on behalf of AVM survivors has become my passion.

Walk with us.