I’ve never known life without Spinal Muscular Atrophy Type II. This neuromuscular disorder progressively weakens muscles over time, stripping me of what little independence I had. Normal day-to-day activities like feeding myself, writing my name, or even using my phone have been lost to me over the years. Since receiving an official diagnosis when I was 13 months old, my family and I have discovered and created inclusive methods for me to survive and thrive in a painfully ableist world. Growing up with a physical disability meant I had to find accessible and entertaining alternatives to the usual activities that most children enjoy. Since I lacked the capability to climb, … Continue reading As My Disability Progressed, I’m Grateful That Games Did, Too