Companion Magazine for IBD Volume 1 | Page 24

and write about my own experience with the disease. I haven’t exactly lived an exciting life, so I figured it was the most interesting thing I could write about. I continued writing short stories about my life with UC and compiled them in a fourth-year course called Making a Book, in which students get to issue their work through a publishing house called Life Rattle Press. I wanted the book to give people who had never heard of ulcerative colitis an idea of what living with the disease is like; something more than a list of the symptoms. Three Tablets Twice Daily was published in 2011. I came up with the title based on the number of 5-ASA pills I took to treat my UC. I wouldn’t say that writing helped me heal, but it did help me cope. It’s difficult to talk to people who don’t know what living with an IBD is like. Telling someone you soiled your pants is not only embarrassing, it doesn’t adequately convey all the difficulties that come with the disease: pain, worry, social isolation, and so on. Writing gave me a chance to really let out all the feelings of anger and frustration and sadness that I had a hard time communicating with the oral word. I think most people have never heard of Crohn’s or colitis. I had never heard of either until I started showing symptoms. So I wanted the book to introduce IBDs to people who had never heard of them, and not in the way that a pamphlet would. Most of the pamphlets I’ve read tend to gloss over just how serious IBDs can be, and they fail to illustrate what it’s actually like to live with the disease. I figured stories about living with UC would give readers a better understanding of the disease and the toll it can take on people. All the stories in the book are my own, and they’re all non-fiction and all of the research and writing and editing and revising combined took about a year.” Rasheed has even helped other members of his family in discovering and accepting their diagnosis. “A relative of mine who has UC only disclosed her condition to me after she read my book. I guess it helped her to know that someone in the family would really understand. Other readers have told me that the book helped them feel as though their experiences weren’t so strange, but in fact relatable to folks like me.” 23