Crohns Colitis And Me

As part of Crohn’s and Colitis Awareness Week (1st – 7th December 2016) the charity Crohn’s and Colitis UK are offering a poster creation app, that lets you build your own poster about how Crohn’s or Colitis impacts you. So here is my poster about how Ulcerative Colitis impacts me and what helps me through.

colitis and me poster MyAnxiety

I am lucky, that I do not have too many flare ups, but when I do, I feel incredibly tired, bloated, get bloody loose stools and have to use Pentasa Enema’s 2 or 3 times a day on top of taking Pentasa tablets twice a day. For me a flare up last for a few weeks, but I become very house bound and have trouble finding the best food to eat and I hate using the Enema’s, but they do help and directly work on the inflammation. As I have said in my poster the care, support and understanding of my wife makes it all a lot easier.

Hopefully this awareness week and the social media campaign of #CrohnsColitisAndMe will help raise the awareness of this invisible disability.

MyAnxiety

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