Avicenna optimum, hand-curated across 6 contextual layers per biomarker.
Curated data · PMID-anchored · T1 (clinical trials) to T6 evidence tiers.
Ferritin 50 means something different for someone who's been exhausted for months than for someone who feels great. We calculate that context, for every marker.
50% discount ends after the 100th signup
THE WAITLIST
Early access
Q3 2026, for the first 100 to sign up.
50% off
Your first blood analysis via our protocol.
Bio Scan priority
First access to your personal recovery path when Bio Scan opens, with elimination and supplement protocols tuned to your markers.
TWO ROUTES
Do you already have a lab report, or are you starting from zero? We have a separate route for each.
Functional lab analysis
Already have a lab report? Upload your data and see the pattern behind your markers right away. We test your values against your own profile: which cofactors are missing, whether your current supplements actually move your markers, and the targeted questions to bring to your doctor. Step out of the uncertainty of 'normal' lab values.
Live from Q3 2026
Bio Scan
Keep hearing 'everything looks fine' while your body says the opposite? Then we stop guessing. We start our own in-depth blood analysis to isolate the exact biochemical cascade. This becomes the foundation for your personal recovery path: a step-by-step, data-driven plan to bring your immune system and energy back to your optimal state. Your roadmap to recovery, phase by phase.
Coming soon, after phase 1
Not feeling your best, but your doctor says 'everything looks fine'?
Upload your lab report. We read the pattern behind your markers and return: whether your current supplements are showing in your markers, which marker is still missing for the full picture, and which questions to bring to your clinician.
Sample, 1 marker
Lab range, Avicenna optimum, your value, and what the pattern says.
Vitamin D3
26 ng/mL
Lab-normal
30 to 100 ng/mL
Avicenna optimum
40 to 60 ng/mL
Pattern
Fatigue cluster, below optimum.
Question we formulate for you
“My ferritin keeps dropping, even with iron supplements. Could we check whether my body is actually absorbing iron, whether there's inflammation somewhere, and whether something is going on with my gut? The analysis I received says these three often hang together.”
Plus per report: cross-patterns across all your markers, follow-up marker suggestions, and ready-to-ask questions for your clinician.
Sample trajectory across multiple uploads. This is how you see where you stand, what changed since your last panel, and how each marker moves over time.
Score in context: marker average minus active patterns
Your own trajectory builds from your first upload. The more panels, the sharper the pattern.
Label, or pattern
A value inside reference ranges can still sit below the Avicenna optimum. That gap between lab range and how you feel is exactly where we look.
Reference ranges answer 'yes or no', not 'is this person functioning'. A marker within the lab range can still sit below the Avicenna optimum. That is why people spend years stuck at 'low normal' without the problem showing up on a single test result.
Markers hang together. When ferritin is low, folate, B12, vitamin D, transferrin saturation and CRP belong on the same panel. One marker alone misses the helpers around it. The whole pattern tells the story, not one number.
Most clinicians compare one marker to the reference range. We read the combination: age, what you have already taken, which helpers are still missing, how your values move over time. Each combination needs a different answer. Generic advice works for some; a large share stays stuck on 'low but okay'.
We measure what you're missing. We bring you back to your optimal state. Your blueprint.
The matrix formula
What we analyse per marker: 6 dimensions together form your unique coordinate.
Avicenna calculates your unique position across all six dimensions, for every marker individually.
Per layer: hand-curated rules, traceable to PMID source
Every marker gets a unique position in our model, weighed across several layers of context at once. Not an isolated number, but the pattern around it.
What this produces per person
What this produces
Answers for those waging a daily battle with the immune system. Sample for a Crohn's profile with malabsorption and cofactor deficit.
T1 = clinical trials · T6 = traditional knowledge. Visible per item.
Per person: 58 foods recommended · 12 trigger categories · 5 supplement routes with PMID
With every upload: how your trajectory moves, which markers respond, and how medication or supplements you input yourself shape your values over time. Each unique or complex signal is personally reviewed by our architect before your portal notification.
THE CORE · AVICENNA ELIMINATION PLAN
Not one list for everyone. No blind experimentation. An elimination plan that shapes around your biomarkers, your triggers, your moment in recovery.
We don't eliminate from a generic list. We map your specific immune triggers via your biomarkers and phenotype-coordinate. The Avicenna Engine reads which food classes your system signals. No generic auto-immune protocol, no one-size-fits-all choice.
For one person, a strict Avicenna baseline is required. For another, we focus on specific cross-reactivity. The strictness adapts to your body. Six blocks we map to your signal, not the other way around.
No guesswork. A data-driven path that removes noise and friction so your gut finds its natural balance. The order of reintroduction matters as much as the elimination itself. We calculate at what layer, at what moment, in what sequence food can come back.
Which food returns at what moment depends on what your markers and phenotype tell us together. Two variables rarely captured in a report.
Pattern clusters we keep seeing, with what we see differently per cluster and the markers we read by default. List grows with every new pattern.
Iron deficiency and T3-conversion block often coexist. TSH alone misses it. Cortisol rhythm reveals if it's HPA-axis driven.
Markers:Iron status, thyroid profile, B12, vit D, magnesium, cortisol rhythm
Elevated homocysteine signals methylation block (B12, folate, B6). More often the cause than vit D alone.
Markers:B12, homocysteine, thyroid, vit D, magnesium, HbA1c
SHBG explains why free testosterone deviates while total reads normal. Cortisol + DHEA-S together reveal adrenal balance.
Markers:Sex hormones, thyroid, cortisol, prolactin, SHBG, DHEA-S
CRP and ESR together distinguish acute from chronic inflammation. Vit D below optimum raises joint pain prevalence regardless of osteoarthritis.
Markers:Vit D, CRP, ESR, uric acid, anti-CCP, RA factor, ANA
Zinc deficiency is often underestimated as an active driver of acne and eczema. Ferritin below optimum stresses skin before anemia shows.
Markers:Zinc, vit D, IgE, ferritin, thyroid, B-complex
Calprotectin differentiates IBD from IBS. Ferritin and B12 together reveal absorption status, not one marker alone.
Markers:tTG-IgA, calprotectin, ferritin, B12, vit D, zinc
High evening cortisol with low morning cortisol points to HPA inversion. Ferritin below 50 disrupts restless-leg physiology.
Markers:Cortisol rhythm, ferritin, thyroid, vit D, magnesium, B6
Insulin and HOMA-IR show insulin resistance years before diabetes diagnosis. Thyroid-conversion block explains metabolic sluggishness at normal TSH.
Markers:Fasting glucose, HbA1c, insulin, HOMA-IR, thyroid, cholesterol panel
Ferritin, transferrin saturation, MCV, MCH, B12, folate
TSH, free T4, free T3, anti-TPO, reverse T3
Cholesterol panel, LDL, HDL, ApoB, Lp(a), homocysteine
ALAT, ASAT, gGT, creatinine, eGFR, urea
CRP, ESR, fibrinogen, ferritin
Vit D, B-complex, magnesium, zinc, iodine
Fasting glucose, HbA1c, insulin, HOMA-IR
ANA, RA factor, anti-CCP, total IgE
21 conditions in our deepest layer. Multiple patterns + protocols per condition. Including patterns generic lab tools usually miss: SIBO subtypes, refractory iron deficiency, Long COVID, MCAS.
T3-conversion block detection, selenium and iron cofactor sequencing
Insulin-androgen cluster, hormonal depth analysis
Chronic iron-loss, inflammation and vit D cluster
Pre-diabetes cluster, fasting insulin triangulation
Liver stress and metabolic pattern
H2 / methane / H2S subtype differentiation, cofactor depletion signal
Malabsorption cluster, pediatric IBD thrombocytosis signal
Incl. refractory pattern, source-of-loss workup priority
Active B12, MMA, functional deficiency detection
Post-acute multi-system cluster, clotting + inflammation + depletion
Chronic inflammatory response biomarker signature
Mast cell activation cluster, tryptase and histamine surrogates
Our base layer covers 160+ conditions, with 21 in the deepest layer. We run continuous R&D, coverage can only expand. Not in this list? Reach out via the waitlist, we will see what fits.
OUR STORY
Your body strives for homeostasis. A measurable state, and a path back to it.
It starts with biological phenotyping. Your phenotype is how your body expresses itself right now, not what is written in your DNA. Two people with the same ferritin can have different phenotypes: one with inflammation, one without. We read that difference by reading the patterns and cascades between all your markers together, not one marker in isolation. Only once your phenotype is clear do we know which disruptors to remove and which cofactors you genuinely lack.
Five functional systems. Severity per axis via color and intensity.
The lab sees one condition label. We see the mechanisms behind it. Real recovery paths start from a detailed map. One is yours.
THE THREE PHASES
01
Elimination protocols on T1-T3 evidence
Before you can rebuild, the storm has to settle. Based on your phenotype we deliberately remove the biological disruptors and overloading factors from your system, temporarily. This gives your gut, your immune system, and your nervous system room to recover.
02
Cofactor routes with PMID source per nutrient
Once there is rest, we restore the foundation. We replenish the exact cofactors and micro-nutrients your phenotype lacks. Your body adapts, rebuilds biological reserves, and you notice your energy systems run more steadily.
03
Retest windows per clinical guideline
A healthy body is a flexible body. In the final phase we bring what was learned back into daily life. We reintroduce stepwise and measure how your biology responds. Goal: a durable, resilient system that holds itself in balance.
Not open-ended. Every phase rests on clinical trials (T1-T3) and cohort validation via the Avicenna Engine™. Every step traceable to a PMID source or guideline.
Fitrah means: the original constitution you were designed with. Our mission is to bring you back to it, marker by marker, phase by phase.
Our Engine grows broader and smarter every week. Every new pattern is curated (T1-T6 evidence-graded), cohort-validated and carefully integrated into the library. No bulk imports, just clinical judgment per expansion. What doesn't match today might match tomorrow: come back any time.
New clinical studies and cohort signals are reviewed, evidence-graded and placed in context.
9 complex conditions added to our deepest analysis layer, smarter cross-referenced with existing patterns.
47 fundamental patterns already covered, basis for every new expansion.
Yes. 'In range' is the broad normal. We read the functional pattern, how your markers move together and which combination points to an upstream cause that individual values miss.
You upload a PDF or photo of your lab report. Within 24 hours you get an online read back: the pattern behind your markers, whether your supplements measurably move your markers, which marker is still missing for the full picture, and the follow-up questions for your clinician.
Fill in the free questionnaire. You'll get your personal blood-values guide right away: per marker the lab-normal range and the Avicenna optimum, with an explanation of why that marker matters for your symptoms. With common BE and NL lab ranges. Plus questions to ask your clinician and ready-to-use phrases for the consult. Saved under your account.
No. We interpret patterns, we don't diagnose. Your clinician stays in charge of medical decisions.
Access as one of the first 100. 50% off your first blood analysis, priority for the personal recovery path once it opens, and updates on the early access launch in June.
The first 100 get early access in Q3 2026. Public launch end of Q3 2026.
Right after upload you see your dashboard and base patterns. For unique or complex signals our architect personally reviews before your portal notification. No 24h promise: every body reacts uniquely, some patterns need extra context.
Your data stays yours. Hosted in the EU, no resale, unsubscribe anytime. We store only what's needed to deliver your analysis.
No, neither. We interpret existing lab reports. For blood draws, go to your clinician or an independent lab. For supplements, use your pharmacy or health store. We give insights and routes, not products and not sales.