Recently I spoke at Rare Disease Day; in 2026, February 28 is the official date for Rare Disease Day. I have been living with myasthenia gravis for 18 years, which is a neuromuscular autoimmune disease that impacts fewer than 1 in 100,000 people
Read MoreIn October 2008, at the age of 24, I was diagnosed and hospitalized for myasthenia gravis, MG, a neuromuscular autoimmune hurricane disease. One of my long-time friends since high school, Ken, told me he would visit me at the hospital right away. I waited. And waited. Two weeks somehow became five years.
Read MoreCome see me speak (virtually) next Tuesday, June 27 from noon to 1 pm CST! I’ll be talking about surviving graduate school when you have mental and physical health challenges. Register…
Read MoreHeads up…things might look a bit wonky on this site as I try to make it more accessible…Also see resources for how to request masks in healthcare settings and how to stay covered with the end of the Public Health Emergency.
Read MoreDoes living with chronic illness ever feel like Groundhog’s Day?
Read MoreCheck out part 2 of my previous post for people who are sick and tired of spending time in the hospital.
Read MoreDo you ever get tired of spending so much time in the hospital?
Read More“What happened to you?” “Were you born like this or did something happen to you?” “Why are you in a wheelchair?”
Read MorePeople often ask me, “How do you stay so positive with all your illnesses?” That’s a very complex question and
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