The choice is yours!
I was diagnosed with IBS in 2011. One year before I graduated college. I had no clue what toll this diagnosis would have on my relatively young life. I have seen many doctors, missed work, and missed major family events due to IBS. I have had to endure physical pain but also mental anguish that I have no idea when I may have a flare. Also, knowing that people in my “village” believe I am not dependable for something I can not control!
8 years later I have gained a new sense of self and I have started accepting the fact that I have done nothing wrong to deserve this and it is not my fault! If anyone believes I am faking and putting on for attention I have developed a new attitude! This new attitude comes with a mission statement: I will have to use the restroom either that will be in the comfort of my home or in the restroom in the space we share. Either way, I will have to go and it is up to you in which capacity you would like to share in my IBS experience!
Community Poll
Does your IBS prevent you from attending public events?
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