- Joined
- Dec 5, 2010
- Messages
- 43
Let's see, apparently I was originally diagnosed with Crohn's when I was a 10-year-old kid. My mum was a nurse and thought my behaviour was odd and that I would often say 'my tummy hurts'. A few tests that I mostly have forgotten (indium scan, barium, blood work) and I thought they said it was 'suspected crohns' and they put me on Asacol and Iron.
I pretty much denied I had the disease from the time I was 13 until I was ... 29! I felt sick a couple times in University, and got some meds, but never stayed on them. Abdominal pain was normal for me so it only seemed weird when it was severe. I still claimed to be a-symptomatic.
Then I started having weird week-end vomiting attacks. (No - it was not from drinking!!!). It seemed like it was related to being nervous/stressed out. It often happened socially, such as when I was visiting family/friends or when they were visiting me. They tested me for a lot of things over two years - "maybe it's your gall bladder", "maybe it's a parasite", "maybe it's gastritis"(sp?), etc. Finally one ER doc said - "maybe it's appendicitis".
I was at a local ER at the time, and was transferred to the ER in the city. After waiting around for a while (getting painkiller for relief thank god!! and anti-nausea for vomiting), I got a CT scan. Apparently, at their first glance at my images, the radiologist said "Whoa - this girl MUST have a history of IBD". It showed significant narrowing and a small-bowel-obstruction, as well as some other stuff.
They gave me a nasal-gastric tube (which I found traumatizing!) and admitted me. I was in the hospital for a week.
That was last January, and I've been on a low fiber-diet, prednisone, azathioprine, and now humira ever since. I have some budesonide in case I need it. I've been having various tests as well. Luckily, my husband is very tolerant and has taken excellent care of me!! I'm thankful I haven't run out of sick days from work too!!
I hated the physical side effects of prednisone (yes I'm vain); but now my joints are hurting - especially my knees. I'm worried about my normal activites - like snowboarding and just walking around. I'm getting really tired of my practically no-fruit, no-veggie no-whole grains diet. Especially when i'm ordering food. I sound like a picky un-healthy person... "white bread and no veggies" BLAH!
Reading some of the other experiences on here, I'm thinking I don't have much to complain about though!!!
I pretty much denied I had the disease from the time I was 13 until I was ... 29! I felt sick a couple times in University, and got some meds, but never stayed on them. Abdominal pain was normal for me so it only seemed weird when it was severe. I still claimed to be a-symptomatic.
Then I started having weird week-end vomiting attacks. (No - it was not from drinking!!!). It seemed like it was related to being nervous/stressed out. It often happened socially, such as when I was visiting family/friends or when they were visiting me. They tested me for a lot of things over two years - "maybe it's your gall bladder", "maybe it's a parasite", "maybe it's gastritis"(sp?), etc. Finally one ER doc said - "maybe it's appendicitis".
I was at a local ER at the time, and was transferred to the ER in the city. After waiting around for a while (getting painkiller for relief thank god!! and anti-nausea for vomiting), I got a CT scan. Apparently, at their first glance at my images, the radiologist said "Whoa - this girl MUST have a history of IBD". It showed significant narrowing and a small-bowel-obstruction, as well as some other stuff.
They gave me a nasal-gastric tube (which I found traumatizing!) and admitted me. I was in the hospital for a week.
That was last January, and I've been on a low fiber-diet, prednisone, azathioprine, and now humira ever since. I have some budesonide in case I need it. I've been having various tests as well. Luckily, my husband is very tolerant and has taken excellent care of me!! I'm thankful I haven't run out of sick days from work too!!
I hated the physical side effects of prednisone (yes I'm vain); but now my joints are hurting - especially my knees. I'm worried about my normal activites - like snowboarding and just walking around. I'm getting really tired of my practically no-fruit, no-veggie no-whole grains diet. Especially when i'm ordering food. I sound like a picky un-healthy person... "white bread and no veggies" BLAH!
Reading some of the other experiences on here, I'm thinking I don't have much to complain about though!!!
