- Joined
- Jun 8, 2008
- Messages
- 223
Has anyone tried this? http://www.nestle-nutrition.com/products/Product.aspx?ProductId=7a542e35-c876-454b-b0a1-b3e8895bcb64 It's an elemental liquid diet I would stay on for 2 weeks.
I know it's not precisely Crohn's related (though I think it can be used for Crohn's). I do have Crohn's but it is mild and under control; I am trying this for what my doctor thinks is a sort of general motility disorder, at her recommendation. Basically, I eat and the food just sits there, resulting in severe bloating and distension. I think the point is to both give my poor bowels a break and to deal with any bacterial overgrowth. I'm so desperate though, I'll do anything to feel better.
Anyway, I'm stressing about the thought of being only able to have this one liquid for 2 full weeks. I'm afraid I might go insane. I also worry about my ability to keep up with school during the process. I asked the nurse if it would affect my energy levels, but she claimed it wouldn't since I'd be getting enough calories. I've just started a new semester and last week was 95% sure I would withdraw and not even try, but decided I should at least give it a shot. But if I'm going to do this treatment, I'm wondering if I should even bother trying to stay in classes. I've been so sick for months, not absorbing nutrients well and constantly sleep-deprived, I can't help but feel like this would tip the scales towards just taking the semester off (especially considering I bike to school every day; it's not far, but you all know what the fatigue can be like when your bowel function is severely impaired). I'm at that point now where I recognize that even if I was miraculously cured today, it would take my body weeks to feel recovered. When I got C. Diff a few years back, I was a lot sicker but for a much shorter period of time, and it still took two months of sleeping 14 hours a night to feel better. But this chronic, every single day illness and constant state of sleep deprivation has put me into a state where I feel like a lot more damage has been done to my system as a whole, and the recovery would take even longer. I really don't know what to do. If anyone has tried Vivonex or something similar, I'd like to hear about what the experience was like (not so much whether or not it helped, since that's a highly individual thing, but rather how you felt during the process and what you did to stay on track with it).
Anyway, I meant this to be a really short post...guess it didn't turn out that way Thanks in advance.
I know it's not precisely Crohn's related (though I think it can be used for Crohn's). I do have Crohn's but it is mild and under control; I am trying this for what my doctor thinks is a sort of general motility disorder, at her recommendation. Basically, I eat and the food just sits there, resulting in severe bloating and distension. I think the point is to both give my poor bowels a break and to deal with any bacterial overgrowth. I'm so desperate though, I'll do anything to feel better.
Anyway, I'm stressing about the thought of being only able to have this one liquid for 2 full weeks. I'm afraid I might go insane. I also worry about my ability to keep up with school during the process. I asked the nurse if it would affect my energy levels, but she claimed it wouldn't since I'd be getting enough calories. I've just started a new semester and last week was 95% sure I would withdraw and not even try, but decided I should at least give it a shot. But if I'm going to do this treatment, I'm wondering if I should even bother trying to stay in classes. I've been so sick for months, not absorbing nutrients well and constantly sleep-deprived, I can't help but feel like this would tip the scales towards just taking the semester off (especially considering I bike to school every day; it's not far, but you all know what the fatigue can be like when your bowel function is severely impaired). I'm at that point now where I recognize that even if I was miraculously cured today, it would take my body weeks to feel recovered. When I got C. Diff a few years back, I was a lot sicker but for a much shorter period of time, and it still took two months of sleeping 14 hours a night to feel better. But this chronic, every single day illness and constant state of sleep deprivation has put me into a state where I feel like a lot more damage has been done to my system as a whole, and the recovery would take even longer. I really don't know what to do. If anyone has tried Vivonex or something similar, I'd like to hear about what the experience was like (not so much whether or not it helped, since that's a highly individual thing, but rather how you felt during the process and what you did to stay on track with it).
Anyway, I meant this to be a really short post...guess it didn't turn out that way Thanks in advance.