I've looked into the SCD diet from SCDiet.org and it excites me to think that this diet could potentially restore my diminished blood cells and get them working properly again to balance my immune system and my weight! Even though having UC or any other IBD is an internal disease that our friends, and family may never see, they can still notice our health externally. And, my weight has lessened no matter how much I eat and stick to a workout plan.
But I'm kind of confused on the SCD diet, because it mentions that sticking to the diet will help stop the over-production of mucus in our gut, but yet... from what I've learned is that when you have UC, its painful because the gut is diminished of its mucus lining due to high acidity levels. At least this was the case for me, and it would make sense for others, since any of us who got this disease started it out with horrible bowel pains.
Also, I question how they allow some of the foods in this diet to be sulfuric (which cause gas/bloating)... But i definitely would consider the diet for sure anyway.
mindoverbutter, just curious is Lialda alot like Asacol meds? Like a maintenance drug? We'll keep in touch for sure.
--Actually now looking more closely at the diet, its pretty much what I ate before seeing my naturopath 2 months ago when I was really active- for her recommended diet regimen (low fiber, no sulfuric foods). What sucks is that soy is in EVERYTHING. Which is not good regardless of UC because it gives off high levels of estrogen in our bodies that we don't need.
One thing I know is that I SERIOUSLY miss my favorite foods: Dark Chocolate, Annie's Cheddar Bunnies & Ben & Jerrys... ahhhhh!
Post Edited (stereofidelic89) : 12/20/2011 8:46:49 PM (GMT-7)