- Joined
- Jan 25, 2012
- Messages
- 16
Hi, I'm 17 years old and I have Crohns. I really don't remember when I was diagnosed, but I do remember the 14 vials of blood they had to take to confirm the diagnosis!
I've had 2 endoscopies and 2 colonoscopies. The last one I had, my Crohns Dr found at least 2 more spots with Crohns. Whoop-pie.
He wanted to put me on Remicade, and when my mom and I read the serious side effects, we were literally crying. This drug gives teens lymphatic cancer.
Now, I'm one of those people that if there's a drug where something bad happens only to 2 people out of 10...I'm one of the two.
Luckily, my Dr read the side effects (cuz my pediatric Dr didn't bother to read them before sending us in a frenzy!) and re-read my reports and decided I'm not quite there yet for the Remicade. He put me on a new drug, which is a steroid, but the side effects are much less....intimidating.
Also, my other Dr (the one I go to for check ups and shots), thought it;s be a good idea to start removing gluten from my diet.
So everything is awfully overwhelming now. I have to watch what I eat
(and I'm not heavy either...so trying to what what I eat should be fun), I can't have greasy food anymore cuz that upsets me, no caffeine *cries*, no dairy, and now no gluten....WHICH IS IN EVERYTHING!!!
So between the list of things I can't have for my Crohns and the list of things I can't have and the list if things that have gluten in them....I feel like I'm left with nothing!!
I really don't mean to complain, but I've just felt really alone with all this and I just have no one else who understands what I'm going through...
I've had 2 endoscopies and 2 colonoscopies. The last one I had, my Crohns Dr found at least 2 more spots with Crohns. Whoop-pie.
He wanted to put me on Remicade, and when my mom and I read the serious side effects, we were literally crying. This drug gives teens lymphatic cancer.
Now, I'm one of those people that if there's a drug where something bad happens only to 2 people out of 10...I'm one of the two.
Luckily, my Dr read the side effects (cuz my pediatric Dr didn't bother to read them before sending us in a frenzy!) and re-read my reports and decided I'm not quite there yet for the Remicade. He put me on a new drug, which is a steroid, but the side effects are much less....intimidating.
Also, my other Dr (the one I go to for check ups and shots), thought it;s be a good idea to start removing gluten from my diet.
So everything is awfully overwhelming now. I have to watch what I eat
(and I'm not heavy either...so trying to what what I eat should be fun), I can't have greasy food anymore cuz that upsets me, no caffeine *cries*, no dairy, and now no gluten....WHICH IS IN EVERYTHING!!!
So between the list of things I can't have for my Crohns and the list of things I can't have and the list if things that have gluten in them....I feel like I'm left with nothing!!
I really don't mean to complain, but I've just felt really alone with all this and I just have no one else who understands what I'm going through...