I had really hoped to be at home by now, spending time with Hubby and the kids during half term. But instead I’m writing this from my hospital bed. Frustratingly there doesn’t seem to be any hope of me going home any time soon and I’m getting a bit fed up. In my last blog I wrote about the steroids rollercoaster that I’ve been on for the last few weeks. This last week has again seen me on IV steroids yet again after having an awful flare up last Thursday. It seems that after a few days on oral steroids my bowel goes “erm, not having that!” and throws a hissy fit. The pain goes off the scale; the only way I can describe it is it feels like I have swallowed razor blades and they’re steadily working their way through my bowels shredding me from the inside out. And then there’s the fun of either having to go to the loo 30+ times a day or the alternative when everything grinds to a halt and nothing comes out. Things were so bad that I ended going down for another CT scan last Friday so...
Life's not been easy since losing my large bowel in 2009. Technically I didn't lose it in the same way you might lose your phone or your wallet- it was removed in an emergency operation after my bowel perforated due to Ulcerative Collitis. Since then I've been on a journey to get back to normal and still don't quite seem to have made it. This blog is a place to share some of the ups and downs, tears and laughter and hospital horrors that make up my life. Enjoy!