My latest musings on Rare Disease about some of the unforgettable bumps and bruises that have occurred as a result of hemophilia. I really love that there is an illustration… Read more

For a long time one of my biggest fears about living with HIV has been the effects on the brain. Several years ago I leaned into that, which unexpectedly led… Read more

With school starting up again, I decided to take the opportunity to discuss one of the biggest hurdles for people living with HIV: disclosure. For many years, I never thought… Read more

Had a ton of fun writing my recent article for Rare Disease, inspired by the What If series of Marvel comics. https://raredisease.net/living/what-if I’m retroactively dedicating this one to Garth McMurray…. Read more

There are a lot of factors as to why I’m able to live the life I am today. Part of being a longterm survivor, for me, is gratitude and understanding… Read more

I have had very active blogging fingers. The last year certainly gave me a lot to write about. Most significantly, the passing of my mom… and her messages to me… Read more

Most of my “medical resume” musings from the patient perspective have been about living with HIV. That’s why I am excited to be contributing to RareDisease.Net, where I’ll be sharing… Read more

This month I got on a plane for the first time since the COVID-19 pandemic started. In the twenty-four years since we’ve been together, this is the longest stretch that… Read more