- Joined
- Jul 23, 2010
- Messages
- 9
feeling bleh
Hey all,
I am 23 and was diagnosed with Crohns at age 7 in 1994. At the time not many people knew what it was, so it took over a year to find a doctor that could tell my parents what was going on. Unfortunately it seems to be pretty common now, when I told people 10 years ago what I had I had to explain it. Now I don't, which is kind of a relief, but it sucks at the same time- I hate that more people are having to going through this.
My mum has been my rock, she is an absolute godsend.
I've been on imuran, salazopyrin, salofalk, prednisone, a liquid and milk based diet when I was 11 that I can't remember the name of, humira and remicade (and probably a few others my parents tried when I was younger, and things I can't remember).
I am currently on imuran, salazopyrin and have a remicade infusion every 8 weeks (though I have had a bad cold for the last few weeks, and am overdue by about 3 weeks and am really feeling it).
Prednisone stopped working over a year ago, so I went on humira and had a localised allergic reaction to the injection site, so I was put on remicade (which the govt. pays for thankfully as all other treatment has failed).
I have been with my boyfriend for about 9 months, and seeing as I have been on remicade for almost a year he has never seen a bad flare up. I am a little afraid I will push him away (as I seem to have done in the past), or it will freak him out (there is little chance of this though-he takes me to all my doc appointments and is incredibly supportive =) ).
I've never really spoken to anyone with Crohns, and I figured it was about time!!! =)
Katie
Hey all,
I am 23 and was diagnosed with Crohns at age 7 in 1994. At the time not many people knew what it was, so it took over a year to find a doctor that could tell my parents what was going on. Unfortunately it seems to be pretty common now, when I told people 10 years ago what I had I had to explain it. Now I don't, which is kind of a relief, but it sucks at the same time- I hate that more people are having to going through this.
My mum has been my rock, she is an absolute godsend.
I've been on imuran, salazopyrin, salofalk, prednisone, a liquid and milk based diet when I was 11 that I can't remember the name of, humira and remicade (and probably a few others my parents tried when I was younger, and things I can't remember).
I am currently on imuran, salazopyrin and have a remicade infusion every 8 weeks (though I have had a bad cold for the last few weeks, and am overdue by about 3 weeks and am really feeling it).
Prednisone stopped working over a year ago, so I went on humira and had a localised allergic reaction to the injection site, so I was put on remicade (which the govt. pays for thankfully as all other treatment has failed).
I have been with my boyfriend for about 9 months, and seeing as I have been on remicade for almost a year he has never seen a bad flare up. I am a little afraid I will push him away (as I seem to have done in the past), or it will freak him out (there is little chance of this though-he takes me to all my doc appointments and is incredibly supportive =) ).
I've never really spoken to anyone with Crohns, and I figured it was about time!!! =)
Katie