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Crohn's Disease the personal side...... cont.


© Susan Johnson

A personal Story about Crohn's Disease I was about four and I remember going to the doctor because I did not feel like going to school with a sore stomach, the doctor looked me over and informed my mother in front of me that I was quite ill......with imaginitis. I was treated this way for many years until my family moved to Australia and I began school. In my first two days in year 8 I was in severe pain and as is normal for kids this age was diagnosed with appendicitis. It was removed and in the process they found the CD. Ever since This I have been able to under stand the reasons for my vomiting and unwillingness to eat due to the pain. I now know that I was not a kid with a big imagination but a kid with something very real and very painful. It has now been 9 years and still I wish I could find that doctor and let him no just what he put me through. I have married and plan on having children but a recent development has made my thinking in that direction change a little. My mother has now been diagnosed as well and this worries me that my children too will have this debilitating problem. I could never knowingly give this to any-one after being a sufferer for so long. I am now in a flare up and my husband is just starting to learn what it is all about. I feel for him and others like him because I can see the uncertain way in which we are treated during this time because they are so unsure of what will cause us pain and what won't. I know its hard not to think of ourselves all the time but it does help to think of them for as long as you can.

---------------------------------------------------------------- NEXT STORY: Hello...I am a 45 year old female who has had Crohn's since age 16. I missed half my junior and half my senior years in high school because I was too ill to go. I was maintained on medication for over a year, but was bed ridden, so I opted surgery to get a better quality of life. At that time I only lost 4 ft of large intestines, and was reconnected. For 5 years, that worked, then I got sick again, and ended up with an Ileostomy. After that I had annual bouts with kinking intestines, which forced 14 additional surgeries through the

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