This is your food, drawn honestly — for your body, not an average person.
A blank stays blank — never drawn as zero.
Where science doesn't know a number, the cell says so.
your nutrients, drawn honestly, never zero
for your body, not an average
This is your food, drawn honestly — for your body, not an average person.
A blank stays blank — never drawn as zero.
Where science doesn't know a number, the cell says so.
What if the plate told the truth — including the blanks?
A blank that stayed blank is reverence — not a zero.
A blank stays blank — never drawn as zero.
Where science doesn't know a number, the cell says so.
A blank stays blank — never drawn as zero.
Seven cells. Some filled. One blank on purpose.
Not measured
| nutrient | coverage | % | you need | basket gives | basis | gap |
|---|
A ribosome reading an mRNA needs the exact amino acid its codon calls for, at the moment it reads it. There is no substitution and no skipping. So the number of complete proteins a meal can build is capped by whichever indispensable amino acid runs out first relative to need — the limiting amino acid. And humans have no storage depot for amino acids: nothing like glycogen for glucose. The surplus cannot be banked. It is deaminated in the liver, its nitrogen fixed into urea and excreted, and its carbon skeleton burned or stored as fat. The excess still delivers calories. It delivers no protein.
The limiting amino acid is a property of the whole day's amino acid supply, not of any single food. The Academy of Nutrition and Dietetics, current position: "The terms complete and incomplete are misleading in relation to plant protein. Protein from a variety of plant foods, eaten during the course of a day, supplies enough of all indispensable amino acids when caloric requirements are met." During the course of a day — not at the same meal. That "combine at every meal" rule was retracted decades ago. So this page will never print an "incomplete protein" warning beside a food: it would be mechanically derived and substantively false.
The claim above comes from published feeding studies. The nine amino acid cells in section 2 come from somewhere else entirely: raw USDA composition, divided by requirements read out of the DRI report. Two routes that share no data. At the default basket they land on the same answer — lysine is the lowest cell of the nine, at roughly half your requirement, while the other eight run from 79% to 123%. Nobody told the arithmetic what to find. If the two had disagreed, this section would say so instead, because a page that only reports its confirmations is not measuring anything.
| hemp preparation | PDCAAS | DIAAS | true digestibility | what it actually is |
|---|---|---|---|---|
| defatted hemp hearts | 44.0% | 0.45 | 90.4% | this is the row that maps to the hearts in your basket — dehulled hemp seed |
| hemp protein concentrate 1 | 42.3% | 0.43 | 91.9% | mechanical air-classification, 66.2% protein |
| hemp protein concentrate 2 | 43.9% | 0.45 | 87.0% | mechanical air-classification, 53.6% protein |
| casein — the reference | 100% | 1.03 | 96.3% | what a score of 1.00 means |
| ↳ Nosworthy et al. 2023, Food Science & Nutrition. Rat bioassay, and that limit ships with the number — rodent digestibility is not human ileal digestibility, and DIAAS is properly defined on the latter. One dissenting paper names tryptophan rather than lysine as limiting, but it studied a single isolate and reported leucine and isoleucine as one combined row, which is not a standard pairing. Two independent sources say lysine; it is named here as lysine with the exception recorded. | ||||
| outcome | design | effect | the authors' GRADE |
|---|---|---|---|
| body weight | randomised trials | 0.37 kg lower | HIGH |
| total cholesterol | randomised trials | 0.15 mmol/L lower | MODERATE |
| systolic blood pressure | randomised trials | 1.27 mmHg lower | MODERATE |
| HbA1c | randomised trials | not significant | LOW |
| all-cause mortality | observational | RR 0.85 | MODERATE |
| coronary heart disease incidence | observational | RR 0.76 | MODERATE |
| type 2 diabetes incidence | observational | RR 0.84 | MODERATE |
| colorectal cancer incidence | observational | RR 0.84 | MODERATE |
| stroke mortality | observational | RR 0.80, CI crosses 1 | VERY LOW |
| the question | the honest answer here | who can check it |
|---|---|---|
| documented | The plan is a file you compose and hold. This page has no account, no server and no database — it computes in your browser and stores nothing. The hive never receives your food log. | You, completely. There is no custodian to trust, because there is no custodian. |
| monitored | By nobody, by design. An operator who watches your intake is a party who can be subpoenaed, breached or sold. Autonomy means every factor is self-verifying — so monitoring is something you do to your own record, not something done to you. | You. This is a deliberate capability we refuse to build, not one we have not built yet. |
| measured | Two things get measured and they are not the same thing: what the food contains (this page, from published composition), and what your body did with it (a blood panel). Only the second is a measurement of you. | Anyone, for the first. An accredited lab under chain of custody, for the second. |
| independently verified |
This is where most of this page is genuinely strong, and where self-report is genuinely worthless. Every requirement traces to a published NASEM value; every food figure to a USDA record ID you can refetch; the EER equation is printed in full. A stranger can recompute this entire page from primary sources and catch us if we are wrong. What no stranger can verify is that you actually ate it. | Anyone with a browser, for the arithmetic. Nobody, for adherence — unless you choose to attach evidence, which is what the ladder below is for. |
| tier | what it evidences | what it cannot support |
|---|---|---|
| 0 · composed | a plan exists and its arithmetic is correct | anything at all about a body. A plan is a hypothesis. |
| 1 · self-reported | your own account of what you ate | the weakest tier in nutrition science and it is not close. Dietary self-report is systematically under-reported, and the error is not random — it varies with body weight, which biases exactly the comparison a page like this invites. Never present a tier-1 result as a finding. |
| 2 · receipt-backed | that the food entered your household — purchase records, a scale reading, a lot number on a bag | that you ingested it, or when. It closes the honesty gap on supply, not on intake. |
| 3 · assayed | what is measurably in your blood — serum 25(OH)D, ferritin, B12, a lipid panel, omega-3 index. The only tier that measures the body rather than the food. | attribution. A changed biomarker does not name its cause; that needs a design, a control and a pre-registered question — which is the BiGen lane, off this page. |