503 603 008




why

MD Piotr Jarecki

what's wrong...

Every month of delay carries a price

0yrs

The average time a rare disease patient spends searching for a correct diagnosis.

EURORDIS 2024; EJHG DOI 10.1038/s41431-024-01604-z

I see this pattern daily. A patient without a diagnosis is not waiting passively — their condition is systematically worsening and treatment costs are climbing. The system does not measure these losses. I do.

Undiagnosed and untreated

The system treats symptoms in isolation, never connecting them into a coherent whole. You cycle between specialists while your condition — instead of improving — steadily declines.

Diagnosed and treated at the source

You receive a targeted therapeutic plan that addresses the root of the problem. Your symptoms are understood in context, and your treatment works with your body instead of against it.

The difference is one step: SYNTHESIS.

What synthesis changes

You are not a case without an explanation. Your story just needs to be put together at last.

A diagnosis does not always fix everything. But it can turn fear of the unknown into a map for decisions.

When scattered results, symptoms, and opinions land on one desk, the case stops being a pile of isolated episodes. It becomes a map: what is known, what is still unknown, what to watch, and where real leverage might exist.

Scattered clues

Case synthesis

Symbolic map: scattered diagnostic clues converge into one case synthesis.

Sometimes the win is treatment, sometimes control, and sometimes knowing how not to lose more ground.

Understand what is happening

Name the pattern and see which symptoms, results, and episodes actually belong together — and which are only noise.

Regain control

Know what to monitor, what to avoid, when to react faster, and how to reduce the risk of losing more ground.

Pursue the right treatment

If a sensible path exists — treatment, rehabilitation, medication, or a change in strategy — pursue it deliberately, not by chance.

If this is what the right direction looks like, why does the traditional path so rarely reveal it?



NOT standard.

The problem is not that doctors do not want to help. The problem is that the system rewards depth without synthesis.

For many common problems, this model works very well. But rare, multi-system, and unusual cases fall outside its natural shape.

"A specialist is a man who knows more and more about less and less."

William J. Mayo

You do not escape a hole by digging deeper. You need a ladder.

Each specialist is right in their own corridor. But the narrower it gets, the less of the whole picture remains.

More depth — less wholeness.

"Concentrate all your thoughts upon the work in hand. The Sun's rays do not burn until brought to a focus."

Alexander Graham Bell

A broad view — focused on one person

You have to see everything: sleep, diet, exercise, psyche, genetics, medications, environment, and disease history. Only then can you narrow your focus to what truly matters for this specific person.

Context reveals what matters. Focus turns that context into a clear course of action.

I know what this system does to an unusual case...
because I lived that odyssey myself.

The new model

Causative Medicine (Aetiiatrics), the wEBMed way.

When a case has been split into fragments for years, one more isolated opinion is often not enough. What is needed is a model: someone has to place symptoms, results, disease history, treatment, genetics, lifestyle, and context on one table — and ask what may connect them. Only then can chaos begin to turn into direction.

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You never change things by fighting the existing reality. To change something, build a new model that makes the existing model obsolete.
Buckminster Fuller

This is not about proving that someone was wrong. Standard medicine does enormous good when the case fits the standard. The problem begins when someone has to see the links between systems, history, genetics, environment, and symptoms. wEBMed was built as a synthesis layer — a model that does not reject science, but applies it more completely.

First the mechanism. Then the direction.

Causative Medicine does not begin with the question: how quickly can we suppress the symptom? It begins with: what may be driving it, what may be maintaining it, and where a real point of influence may exist. Sometimes this leads to a concrete diagnosis. Sometimes to better symptom control. Sometimes to a decision about what to investigate next. But the goal is always to move from chaos to a model that can support the next step.

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A physician is obligated to consider more than a diseased organ, more even than the whole man — he must view the man in his world.
Harvey Cushing
Examples of causative thinking
Example 1 — nervous system and environment
late work and 4–5 hours of sleepmorning fatigue, irritability, muscle pain, brain fogrepeated “normal results”chronic activation of the hypothalamic–pituitary–adrenal axisflattened cortisol rhythm and sympathetic dominancehyperalgesia, dysautonomia, mood dysregulationcorrection of sleep, light, exertion, nutrition, and workloadmore energy, less pain, better regulation

Sometimes the breakthrough is not a rare diagnosis, but recognizing an overloaded regulation system and rebuilding physiology so the body can recover again.

Example 2 — urea cycle and nitrogen
vomiting, sleepiness or confusion after a larger protein load, fasting or infectionalmost normal tests between episodessuspicion of impaired nitrogen detoxificationammonia, plasma amino acids, urine orotic acidOTC variant and ornithine transcarbamylase deficiencyhyperammonemia from urea-cycle failurenatural protein limit, anti-catabolic calories, citrulline/arginine, benzoate or phenylbutyratefewer crises and a clear sick-day protocol

In a urea cycle defect, diagnosis translates into concrete decisions: how much protein, how to avoid catabolism, what to do during infection, and when to use nitrogen-scavenging treatment.

Example 3 — Behçet and multisystem inflammation
recurrent oral ulcers and inflammatory flaresgut pain, joints, skin, eyes, vessels or neurologic symptomsseparate consultations without one modelneutrophilic inflammation and vasculitis patternsuspicion of multisystem Behçet diseasecolchicine, steroids, azathioprine or other immunosuppressionintolerance or insufficient response to TNF-α inhibitorsJAK inhibitors and disease-activity monitoring

In Behçet disease, connecting oral ulcers, gut, skin, joints, eyes, vessels, and neurologic symptoms can turn “strange separate problems” into a recognizable inflammatory pattern with a concrete treatment path.

This way of working has a name: wEBMed. It is not a slogan — it is a map of three layers that must work together.

web

web / network of dependencies

A person is not a collection of separate organs. Symptoms, results, systems, history, and environment form a network that has to be seen together.

EBM

Evidence-Based Medicine

Decisions should come from data, biology, mechanisms, and scientific literature — without magic, shortcuts, or pretending certainty.

ed

education / explained

The patient should understand why something is being done. Explanation is not an extra — it is part of regaining control.

Causative Medicine (Aetiiatrics) is not an alternative to science — it is a fuller application of it. The body is a network of interdependent systems, not a collection of independent organs. When one system is overloaded, effects appear in places that appear to have nothing to do with it. My work is to find the critical node in that network — and fix the mechanism, not just silence the symptom.

Systems thinking

Systems thinking means considering simultaneously: biological state (genome, inflammatory markers, gut axis, hormones), psychological state (stress, emotional regulation, trauma history), behaviours (sleep, nutrition, movement, supplementation), and environment (toxins, exposures, microbiome). Only the whole gives the full picture. Rare diseases are rare one by one, but together they affect a vast number of people. Every well-described case increases the chance that the next person will not be left alone with chaos.

checklist
01

Application and initial qualification

Before we meet, I review the submitted information and initial documentation. I assess whether your case falls within my area of competence and whether the Causative Diagnostics Package is the right step at this stage. This is not an exclusion screen — it is a fit screen.

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You know your case has been preliminarily reviewed and that working together makes sense.

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02

Documentation gathering and audit

You submit all available medical documentation: discharge summaries, test results, imaging, genetic results, treatment history. I am not interested in a "summary" — I am interested in raw data. Every result is read, indexed, and placed on a timeline.

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Your medical history becomes an organised, coherent resource — seen in full by one person for the first time.

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03

Deep diagnostic interview

The interview session lasts significantly longer than a standard consultation. I ask questions others do not: about the sequence of symptoms, temporal connections, what improves and worsens the condition, genetic and family context. I listen not only to what you say, but to what you do not say.

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You feel heard in a way you have not previously experienced in a medical setting.

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04

Synthesis and visual explanation

I combine data from documentation, the interview, and genetic analysis into a coherent causal model. I identify the mechanisms connecting your symptoms. I prepare a visual causal map — a diagram showing how the elements of your case are linked. This is not a list of diagnoses. It is an explanation of the architecture of the problem.

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For the first time, you see your case as an understandable pattern, not a random collection of unrelated complaints.

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05

Written synthesis and action roadmap

You receive a premium written case synthesis: medical history, visual causal map, diagnostic and therapeutic priorities, specific recommendations with scientific rationale, and a plan of next steps. This is your working document — you can present it to any new doctor and expect them to understand where to begin.

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You have a written plan. You know what to do. You have a tool for further work with other specialists.

Hope begins when a model appears.

Without understanding the mechanism, what remains is chaos: more visits, more results, and more conflicting suggestions. When the dependencies begin to appear, decisions become possible: what to test, what to rule out, what to monitor, what to relieve first, and where to look for treatment. This is not passive waiting for a miracle. It is regaining direction.

The body as a map of dependencies

This is not a list of organs. It is an architecture of connections.

The 3D model shows what a standard visit rarely makes visible: a human being is not a collection of separate parts. Systems, organs, tissues, metabolism, hormones, immunity, nerves, vessels, and environment form one network. Causative Medicine tries to organize that network for one specific person.

Rotate, zoom, explore — body complexity as a map of the case.

In your written synthesis, this idea becomes a personalized map: symptoms, results, organs, systems, and hypotheses connected by causal lines, not a list of random diagnoses.

psychology

The biopsychosocial model is part of my thinking — I consider body, mind, and behaviours together. But the front-door promise is precise: diagnostics, synthesis, map, and plan. Foundations — sleep, nutrition, movement — appear where they are clinically relevant.

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Every stage of this path is designed to end the chaos and begin building clarity — step by step, with precision.

Fit

Check whether this is the right process for this situation.

This is a paid medical synthesis process: I read the whole case, connect the pattern, and set a usable direction. The filter below helps you decide whether this level of work fits your situation.

This package is for you if:

  • check

    You are exhausted by 15-minute visits

    You want the deepest medical analysis available, not another quick opinion based on one fragment of documentation.

  • check

    You value structured data, true EBM, and due diligence

    You expect facts to be organized, evidence-based medicine to be real, and the work to be done carefully rather than quickly.

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    You understand real medicine takes time

    You know difficult cases are not solved in five minutes — and focused physician time is expensive.

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    You may be the family organizer or advocate

    This may be your own odyssey or your fight for a parent, partner, child, or someone who no longer has the strength to manage the case alone.

  • This package is not suited for:

  • close

    You expect miracles, a magical pill, or pseudoscience

    This is not an alternative promise of healing. It is medical analysis, synthesis, and work on facts.

  • close

    You want a quick free email consultation

    A years-long medical history cannot be responsibly analyzed in five minutes or for free over email.

  • close

    You are not willing to gather documents or change habits

    This process requires material to analyze and readiness to act. Without documentation and cooperation, there is no synthesis.

  • close

    You need emergency care or advice outside the process

    I am a Medical Doctor performing highly specialized work. I am not an ER, and I do not provide free medical advice over email. If you want my brain on your case for 10–100 hours, you must book the process.

  • Not ready for the process yet? Start by organizing your documents.

    Do not send a years-long medical story by email asking for a free assessment. First, use the educational material and prepare a timeline, results, discharge summaries, and questions.

    Start with educational materialopen_in_new

    Educational material does not replace a consultation and is not individual medical advice.

    Frequently asked questions

    A good candidate is a patient with a long, unresolved, multi-system health problem — someone who has accumulated medical documentation and is looking for someone to synthesise the whole picture. If your primary goal is a quick prescription, a quick referral, or confirmation of a single diagnosis — this package is probably not the right step at this stage.

    "Everything" usually means many isolated consultations — but not synthesis. A comprehensive documentation audit, deep interview, and systems thinking are qualitatively different from another specialist visit. Many of my patients come precisely after "everything" has failed.

    The package is available entirely remotely. Documentation is submitted electronically, the interview takes place via video call, and the written synthesis is delivered digitally and in print form. You do not need to be in Poland or any specific city.

    The documentation audit typically takes 3–7 business days before the interview session. The interview itself lasts as long as we need. The written synthesis is ready within 5–10 business days after the session, depending on case complexity.

    Your data is processed in accordance with GDPR and medical data protection regulations. Medical documentation is stored securely and used exclusively for your diagnostic process. Details can be found in the Privacy Policy.

    Yes — this is one of the primary purposes of the document. The written synthesis with scientific rationale is designed so that any new specialist can understand the case history without you having to re-explain everything from the beginning.

    The package covers diagnostics, synthesis, and a roadmap — not direct treatment. It includes recommendations for next therapeutic steps that you can implement independently or with the help of chosen specialists. Webmed is not a treatment practice — I am a diagnostician and guide, not a long-term treating physician.

    Proof of competence

    Briefly: this is a physician built for complex cases.

    verified

    Tens of thousands of consultations and years working with difficult medical histories.

    verified

    Personal experience of a diagnostic odyssey — without turning this section into a second biography.

    verified

    The ability to read the whole: records, timeline, family risk, genetics, and patterns.

    I read everything. I take the whole case seriously. I will not rush you.

    You can see this kind of analysis in the PACNS patient story — as an example of reasoning, not a promise of outcome.

    What remains after the process

    Direction, not a guarantee.

    Honesty instead of false promises.

    Medicine gives no guarantees. A final diagnosis may still escape us, and treatment may remain difficult. I do not promise miracles — I promise the deepest analysis modern medicine can offer.

    Even if we do not find a magical cure, you leave with direction. We separate signal from noise. We rule out dead ends. You move from 1/10 to 3/10. You gain the peace of knowing that EVERY stone was turned by a physician. Knowing what this is NOT can be as valuable as knowing what it is.

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    Structure: Your medical story organized for the first time in your life

    visibility

    Clarity: You know what has already been ruled out and why

    route

    Direction: Concrete next steps instead of vague recommendations

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    Peace: Confidence that everything possible was actually done

    description

    Tool: A one-pager to give every future doctor

    This is not a promise of a miracle. It is a promise that you will not be left alone with chaos.

    How the process works

    One path: order, direction, fit.

    Instead of separate walls of documents and package copy, this section shows the process: what we organize, how we choose next steps, and what remains in your hands after the work is done.

    You are not buying paperwork. You are buying synthesis.

    You are investing in my time, focus, and experience. I will analyze every page of your history, connect the dots the system had no time for, and set a concrete direction.

    account_tree01 / ORDER

    A single story emerges from document chaos.

    First we organize the past: results, discharge summaries, imaging, consultations, genetics, family risks, and timeline. The goal is a map that can be understood without starting from zero.

    check_circleComplete Epicrisischeck_circleGenetic Reportcheck_circleOne-Pager Summarycheck_circleGenetic Family Tree
    route02 / DIRECTION

    You know what makes the most sense next.

    Then we separate dead ends from leads that need closure. The result is prioritized diagnostics, differential diagnosis, and justified treatment where it makes clinical sense.

    check_circleDifferential Diagnosischeck_circleRecommended Diagnosticscheck_circlePrescriptions
    verified03 / FIT

    The process has to fit the real life of the patient or caregiver.

    Finally we translate conclusions into prevention, lifestyle, working goals, and material you can bring to future doctors.

    check_circleProphylaxis Recommendationscheck_circleLifestyle Plancheck_circleSFBT & MI Goals
    FLAGSHIP ARTIFACT

    One-Pager: stop retelling the same story from zero.

    One page for future doctors: the problem, timeline, key findings, diagnoses to consider, red flags, and next steps. It is the most important anti-chaos document in the whole process.

    star

    You bring it to every future consultation.

    star

    It reduces case handoff from 40 minutes to a few.

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    It protects key details from getting lost.

    eventBefore the visit

    You receive a guide for organizing your medical history: tests, discharge summaries, imaging, consultations, and key dates.

    event_availableAfter the visit

    You also receive a practical basics guide for health: eating, sleep, movement, supplementation, and daily habits.

    · Document analysis· Medical synthesis· Diagnostic priorities· Materials for future doctors
    Decision

    If this is your situation, choose a path.

    The full process, or paid triage if you are unsure where to start.

    Our offer

    Three paths. One decision.

    From 20 minutes to ~100 hours of my time. Choose the level that fits your situation.

    Qualification

    Online, calendar-based

    250 PLN

    One-time fee — not credited toward higher packages

    A short decision call to assess whether this model of work fits your situation.

    Online20 min callQ&A

    What's included

    Initial assessment of situation and documents
    Answers to patient questions
    Recommendation of the right path
    Educational materials — digital version

    You choose the slot in the online calendar.

    Most chosen

    Advanced Diagnostics

    Online, with written report

    4,000 PLN

    Online process — final price, no hidden costs

    In-depth diagnostic work for complex health histories, large result sets, and patients who need a clear next-step plan.

    Most chosenOnline~10 h physician work<48 hPL/ENPrinted report

    What's included

    Medical documentation review and organization
    Differential diagnosis (DDx)
    PDF report <48 h
    Plan of next steps
    Documentation in two languages
    Personalized prevention plan

    Delivery: <48 h from the interview with complete documentation.

    VIP Coordination

    Home visit and remote coordination

    40,000 PLN

    Final price — includes travel within Poland

    Highest-support option: advanced diagnostics, a home visit, and 30 days of remote coordination.

    ~100 h physician workHome visit <7 daysResponse <24 hUp to 8 consults

    What's included

    Everything from Advanced Diagnostics
    Home visit anywhere in Poland
    30 days of remote coordination
    Direct communication with response <24 h
    Up to 8 follow-up consults
    ~100 h of physician work

    Home visit: <7 days. Remote coordination: response <24 h.

    Detailed comparison

     QualificationAdvanced DiagnosticsVIP Coordination
    Initial assessment of situation and documents
    Answers to patient questions, worries, and doubts
    PDF report delivered online (<48 h from interview)
    Follow-up consults after report delivery (up to 8)
    Home visit anywhere in Poland (<7 days, travel included)
    Review and organization of all medical documentation
    In-depth online diagnostic interview
    Differential diagnosis (DDx) with list of ruled-out and suspected conditions
    Systemic biological, psychological, and behavioural analysis
    Solution-Focused Brief Therapy (SFBT) techniques
    Lifestyle modification through habit change coaching
    Personalized, evidence-based supplementation recommendations
    Clinical interpretation of genetic data (if available)
    Genetic counseling
    Pharmacogenomics — drug-gene interactions (if test scope permits)
    Printed, stamped report
    Physical delivery (Poczta Polska / InPost)
    Documentation in two languages
    Healthy lifestyle educational materials (diet, sleep, exercise) — digital
    Educational materials — printed version
    Clear relationship diagram connecting symptoms and results
    Plan of next steps and priorities
    Genogram / family tree (if indicated)
    Targeted genetic-region interpretation
    Comprehensive sleep, nutrition, and physical activity assessment
    Personalized health, cancer-prevention, and monitoring plan
    Public healthcare navigation support (if applicable)
    Medical certificate for ZUS/KRUS and disability boards
    30 days of remote coordination and care (response <24 h)
    Sequencing costs (WGS, genetic panels)
    Emergency care

    All prices are final patient prices. The 250 PLN qualification fee is a separate service and is not credited toward the Diagnostic Synthesis package or VIP Coordination. Service descriptions are for informational purposes and do not constitute a guarantee of diagnosis, cure, or approval of ZUS/KRUS/disability benefits. Detailed terms in the Terms of Service.

    An anonymized clinical case

    A rare PACNS case. When “neurodegeneration” turned out to be CNS vasculitis.

    One real, heavily anonymized story showing why difficult cases require synthesis, not another quick opinion.

    Adult maleRapid deterioration over about 2 monthsSeveral strokes in a short periodNeurology departments and university clinicsGuillain-Barré syndrome consideredPACNS / primary angiitis of the CNS
    ≈1–2.4 / 1,000,000estimated annual PCNSV/PACNS incidence

    This disease is so rare that it can disappear under the labels of neurodegeneration, psychiatry, or “unclear changes”.

    This was my case. Over about two months, the patient deteriorated rapidly: he was admitted to one hospital, then another center and another, with Guillain-Barré syndrome among the suspected diagnoses. He suffered several strokes in a short period. The records contained clues, but each clue alone was insufficient. Only when they were connected into one map and the CNS vasculitis hypothesis was formed did the right path open.

    What synthesis looked like

    01hub

    Broad differential

    Several paths had to be considered first: APS, infection, autoimmune encephalitis, neuro-Behçet, mitochondrial disease, and vasculitis.

    02rule

    Weak signals de-emphasized

    Isolated low-titer anticardiolipin IgG did not explain the whole case. It had to be closed properly, but it could not become the central diagnosis.

    03neurology

    Inflammatory-vascular pattern

    Progressive deficits, repeated stroke events, and the overall pattern increasingly shifted the reasoning toward CNS vasculitis — rare, severe, and easy to miss.

    04emergency

    A prognosis-changing decision

    In cases like this, time matters: the right diagnosis opens the path to aggressive immunosuppressive treatment before injury becomes irreversible.

    The turning point

    Instead of treating the symptoms as "another unexplained neurological problem," I made the diagnosis of CNS vasculitis and immediately organized urgent admission to the rheumatology unit. The patient went straight to the hospital after my consultation. That was the moment the fragments stopped being fragments.

    What happened next

    After initiating aggressive immunosuppressive treatment — high-dose glucocorticoids and cyclophosphamide — under specialist care, the patient survived, the disease was stopped, and he is functioning much better today. Permanent neurological deficits remain. Without the right diagnosis and treatment, he most likely would not be alive now. This is not a promise of the same outcome for everyone — it is an example of how finding the right mechanism and immediate, organized escalation can completely change the trajectory of a case.

    In difficult cases, the missing piece is not always more data. Sometimes it is the person who can see the pattern before it is too late.

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    A conversation with the patient

    Coming soon: an interview with the patient about the journey from worrying symptoms, through months of consultations, to diagnosis and treatment that saved his life.

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    This story is intentionally anonymized: no name, city, institution names, dates, or details that could identify the patient.

    This is a single clinical story, not a guarantee of diagnosis, treatment, or survival. Every case requires individual assessment.

    🚧 Site under construction — full version coming soon