Loving the recipes, just starting week one. Completely over bought. Have to really pay attention going into week 2 to watch portion and servings. I am only feeding two for dinner and on my own for breakfast and lunch. The one recipe breakfast this week was enough for four days. Is it ok to eat the same thing for a couple days, breakfast and lunch, and not follow the schedule to the T?


The main benefit of Whole30 though is to see how certain food groups affect your body. If you normally eat everything, you'll never really know if dairy may be making you bloated or if grains may be upsetting your stomach. By cutting out most of the food groups and processed foods for 30 days and slowly reintroducing them into your diet, you'll be able to spot which foods are doing what to your body. 

^ Hou JK, Lee D, Lewis J (October 2014). "Diet and inflammatory bowel disease: review of patient-targeted recommendations". Clinical Gastroenterology and Hepatology (Review). 12 (10): 1592–600. doi:10.1016/j.cgh.2013.09.063. PMC 4021001. PMID 24107394. Even less evidence exists for the efficacy of the SCD, FODMAP, or Paleo diets. Furthermore, the practicality of maintaining these interventions over long periods of time is doubtful.

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Before I went on Whole30 I was sleeping 8 to 10 hours a night (yes, I love my sleep), yet come 2 p.m. I'd hit an energy slump. I'd feel high right after I ate (looking back on it, probably because I was eating so much added sugar) but my energy would significantly fluctuate through the day. During the beginning of Whole30 — specifically the first three days — I really struggled. Again, I was a sugar addict and I think detoxing from that really affected my energy levels. But after that slump, my energy was constant — I really had never felt better. Even when things didn't go the way I wanted, I felt energetic and up for any challenge.
The WHO trial (so named because the international team of principal investigators contained World Health Organization members) tested the potential of clofibrate, a “pre-statin” cholesterol-lowering agent, to reduce heart attack morbidity and mortality. The investigators ultimately concluded that clofibrate "cannot be recommended as a lipid-lowering drug for community-wide primary prevention of ischaemic heart disease.” Nevertheless, clofibrate remained in use until 2002, when it was pulled for increasing cancer rates. In their review of studies such as the WHO trial, Uffe Ravnskov and David Diamond observe, “Despite the largely disappointing findings from 50 years of cholesterol lower[ing] trials, the indictment and conviction of cholesterol as the causal agent in CVD [cardiovascular disease] has stood the test of time. … [Yet] the grand effort to reduce cholesterol as a strategy to improve health has failed.”
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