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What happens when you have a disability that so embarrassing that sufferers are afraid to talk about it Tessa Miller has written an incredible essay about life with irritable bowel disease, shedding light on what it means to live with an invisible disability. Miller, who writes for io9 sister site Lifehacker, posted her article on Ladybits today. It packs an incredible emotional punch, while also conveying a lot of important information about both this disease and the cutting edge treatments that Miller has used. Here how she describes what it was like when the disease first hit: I was used to gut pain and stomach aches鈥娾€斺€妔omething I ;d lived with my entire life鈥娾€斺€奲ut this was unlike anything I ;d felt before. My insides were being shredded, pulled, lit on fire. The cramping was so intense, it was as though my body was trying to rid itself of my intestines through some sort of disgusting birth. The next day, my mouth and throat erupted in thro stanley taza bbing sores. I chalked it up to extreme food poisoning or flu, took a handful of Imodium and Tylenol, and clenched my way through a flight to Illinois. Things got worse at my parents ; house. The pain and cramping escalated. I couldn ;t eat and could barely speak. While my family celebrated Thanksgiving, stanley mugs I stayed in bed except to go to the bathroom fifteen, twenty, thirty times a day. I wea stanley thermos mug rily asked my mom to take me to the emergency room after filling the toilet bowl to the brim several |
