I don’t know how to describe it. There is just something about being constantly told I should talk about my disability that makes me uncomfortable. I recognize, and am often reminded, that many people with cerebral palsy have difficulties communicating. I’m repeatedly told that I should use my ability to speak as an asset to spread awareness and information. At the same time, cerebral palsy is so varied that my experiences are likely to be drastically different from the next person. I will add to the conversation if someone asks me directly, or I’m impacted, but I’m not too sure about otherwise…