Your journey begins: biio.markers assessment

biio.markers is a comprehensive initial assessment for people with complex invisible illness: conditions that cross body systems, specialities or diagnoses.
Available Australia-Wide
No Referral Required
Coordinated Care
Report Included
In real life

One body. One set of signals — felt together, all at once.

At biio.markers

The same signals, gathered and treated as information.

In real life → at biio.markers

The same signals, felt all at once, gathered and treated as information.

The right starting point if your health has not fitted neatly anywhere else

biio.markers is step one—where an expert clinician reviews your history, symptoms and patterns across body systems. If diagnosis remains a question, you'll review formal clinical criteria and complete targeted testing in consult.
The assessment gathers the picture that fragmented care often leaves scattered, treats your story as valuable information, and make the key questions clear for the right people to work on them.
You may be here because:
you have symptoms that change with posture, food, sleep, exertion, heat, stress, sensory demand, infection, hormones or recovery;
you have been told your tests are normal, but your body is still not functioning normally;
you have partial or suspected diagnoses that have never been connected into one plan;
you suspect connective tissue, dysautonomia, immune, post-viral, neurodivergent, hormonal, pain, fatigue or functional impacts may be involved;
you already have a diagnosis, but it does not explain the whole pattern

Which biio.markers assessment is right for me?

Enter biio.markers guided by your most pressing questions. The assessment names where to start; it does not decide what care plan follows. You clinician will adapt your assessment dynamically based on your priorities at the time.

Signature biio.markers

60 min
$240
Your Clinician
Allied health practitioner with special interest in complex invisible illness. Experienced across all pathways and major conditions.
Key Question
What do my symptoms mean, and where should I begin?
What's Assessed?

Choose this if you're already diagnosed, not sure where to start or simply seeking a board first assessment across systems for unexplained symtoms. We'll review:

  • your full health history;
  • the main symptoms and systems currently affecting you;
  • existing diagnoses, suspected diagnoses and previous investigations;
  • medications, supplements and previous treatment attempts;
  • what remains unclear;
  • which biio. therapies, clinicians or clinical pathway may be most appropriate next.
Next Steps
You’ll receive a comprehensive report and care plan, including recommended next appointments, a suggested biio. care team, self-management considerations, and further investigations or referrals where indicated.
Limitations
This assessment is designed to orient your care and make sense of the whole picture. It does not include the detailed connective-tissue criteria review, orthostatic testing, immune/post-viral review, or formal diagnostic work included in longer biio.markers appointment types.

Connective Tissue biio.markers

90 min
$320
Your Clinician
Physiotherapist with special interest in hypermobility, connective tissue disorders and complex invisible illness.
Key Question
Do I have hypermobile Ehlers-Danlos syndrome, hypermobility spectrum disorder, a rare EDS subtype, or another heritable connective tissue disorder?
What's Assessed?

Everything covered in the Signture biio.markers assessment, plus detailed assessment of connective tissue and hypermobility features. This assessment may cover:

  • review against hEDS diagnostic criteria;
  • hypermobility history, subluxations, dislocations, soft tissue injury or chronic musculoskeletal pain;
  • skin, tissue fragility, bruising, scarring or wound-healing features;
  • screening for features and family history that may suggest a rare EDS subtype or another heritable CTD;
  • whether genetic counselling, genetic testing, rheumatology review or another specialist referral may be needed;
  • how connective tissue findings may relate to autonomic, gastrointestinal, immune, fatigue, pain, hormonal or neurodivergent features.
Next Steps
You’ll receive a report documenting your connective tissue findings, whether your presentation appears to align with hEDS/HSD criteria, whether genetic or specialist escalation is indicated, and a comprehensive care plan.

If formal medical diagnostic review is needed, your clinician will recommend the appropriate next step. If you do not meet formal criteria, your report will still name what was found, what remains uncertain, and what support may be appropriate.
Limitations
This assessment can help identify whether your presentation aligns with hEDS/HSD criteria. It does not replace a formal medical diagnosis where specialist sign-off is required for NDIS, insurance, legal, school or work purposes.

Dysautonomia biio.markers

90 min
$320
Your Clinician
Physiotherapist or Exercise Physiologist with special interest in dysautonomia, orthostatic intolerance, post-viral illness and complex invisible illness.
Key Question
Do I have POTS, orthostatic intolerance or another dysautonomia pattern, what phenotype may be driving it — and what might help?
What's Assessed?

Everything covered in the Signture biio.markers assessment, plus detailed assessment of autonomic dysfunction features. This assessment may cover:

  • symptoms of POTS, orthostatic hypotension, or related patterns;
  • a NASA Lean Test protocol where clinically appropriate;
  • review of heart rate, blood pressure and symptom changes with posture;
  • heat intolerance, exercise intolerance, post-exertional worsening, presyncope, faintness or palpitations;
  • clinical review of POTS subtypes (hypovolemic, hyperadrenergic, neuropathic) so care can be directed more precisely;
  • contributing features such as connective tissue variation, immune activation, deconditioning, post-viral change, trauma physiology, hydration, salt tolerance, sleep, medication effects or hormonal interaction.
Next Steps
You’ll receive a comprehensive report of autonomic and orthostatic findings, along with care recommendations, suggested next appointments, a recommended biio. care team, and further investigations where indicated.

If the findings suggest medical review is needed for diagnosis, medication or cardiac investigation, our medical practitioners will be available to you.
Limitations
This assessment helps identify whether your presentation aligns with POTS, orthostatic intolerance or another dysautonomia pattern. It does not replace medical diagnosis or cardiac investigation where those are required.

Multi-diagnostic biio.markers

120 min
$400
Your Clinician
Physiotherapist with special interest in complex invisible illness. Experienced across all pathways and major conditions.
Key Question
Are connective tissue features interacting with dysautonomia and/or immune or post-viral features in my presentation — and what can I do about it?
What's Assessed?

This two-hour assessment is for presentations where the multiple diagnoses, across pathways, are suspected and require investigation. It will cover:

  • everything included in Signature biio.markers;
  • connective tissue features, hEDS criteria, rare subtype screening;
  • dysautonomia and orthostatic testing (NASA lean testing);
  • immune or post-viral features, PEM and MCAS-pattern review;
  • relevant neurodivergent, hormonal, gastrointestinal, sleep, pain or fatigue factors where they affect the main clinical question;
  • existing investigations and what they do or do not explain;
  • which clinical pathways, practitioners or external specialists should support
Next Steps
You’ll receive a comprehensive report that separates the major clinical questions, documents what was found, names what remains uncertain, and recommends a staged care plan.

Your plan may include a recommended biio. care team, formal medical or specialist review where needed, further investigations, and sequencing advice so you are not left trying to do everything at once.
Limitations
Multi-diagnostic biio.markers is not for “more symptoms” by default. It is for presentations where connective tissue features are interacting with dysautonomia and/or immune or post-viral features and enough time is needed to assess those relationships properly.

Neurodivergence biio.markers

90 min
$320
Your Clinician
Allied health clinician with experience in neurodivergent health, sensory processing, developmental considerations and functional capacity.
Key Question
How are neurodevelopmental, sensory, executive function and body-system factors affecting my health, capacity and care access?
What's Assessed?

Everything covered in Signature biio.markers, plus detailed review of neurodivergent health considerations. This assessment may cover:

  • ADHD, autism, AuDHD or suspected neurodivergence;
  • sensory differences, overwhelm, shutdown patterns or recovery needs;
  • executive function, attention, planning and daily capacity;
  • neurodivergent burnout and loss of function;
  • ARFID, restricted eating, appetite cues or food-related barriers;
  • overlap with pain, hypermobility, dysautonomia, gastrointestinal symptoms, immune activation, sleep disruption or hormonal changes;
  • what support may be needed from occupational therapy, psychology, dietetics, psychiatry, GP, paediatrics, school, work or other services.
Next Steps
You’ll receive a report that documents sensory, developmental, executive function, functional capacity and body-system considerations where relevant.

Your care plan may include recommended biio. practitioners, accessibility considerations for future appointments, practical capacity supports, dietetic or occupational therapy input, psychology or medical review, and external assessment or referral where indicated.
Limitations
This assessment is not a standalone formal ADHD or autism diagnostic assessment. It does not replace psychiatry, paediatric, neuropsychological, school, workplace or NDIS-specific assessment where those are required.

How we think and assess—mechanism before labels

The biio. model

Six mechanisms — not six diagnoses. What the body is doing, beneath the labels.

At biio.markers

Every assessment reads the whole picture through all six.

Hover a mechanism to see how biio. supports it

What happens before, during and after your appointment

Our carefully crafted diagnostic pathway transforms years of medical uncertainty into clear answers through systematic assessment that honours both your lived experience and the latest clinical science.

Questions? Here's everything you need to know

Have we missed something? Click the chat icon in the bottom right corner and we'll be happy to help.

Booking and fit
Do I need a referral to book?

No. You can book a biio.markers assessment without a GP referral. You only need a GP referral if you want to claim a Medicare rebate through an eligible chronic condition management arrangement.

I do not know which biio.markers to choose. What should I book?

Choose the 60 minute signature (universal) biio.markers assessment if you are unsure. You can always add further assessment in a second appointment.

Choose the 120-minute multi-diagnostic assessment if you are undiagnosed and your history clearly involves connective tissue features plus dysautonomia and/or immune or post-viral features.

Choose hormonal if your main question is hormonal, menstrual, pelvic, thyroid, testosterone, sleep or circadian rhythm change.

The starting point helps us understand your first concern. It does not decide your whole care plan. Your clinician can help identify which practitioners, therapies or pathway should take responsibility for the next step after your assessment.

Is this only for people with a diagnosis?

No. Some people come to biio. with confirmed diagnoses. Some come with suspected diagnoses. Some come with years of symptoms and no clear explanation. biio.markers is designed for people whose health picture needs to be gathered and reviewed before the next step can be chosen.

Is this suitable if I already have a diagnosis?

Yes, if your diagnosis does not fully explain what is happening now, or if you need a clearer management plan and care team. A diagnosis can help name part of the picture. It does not always explain why symptoms change, why function has declined, what else is involved or what should happen next.

Is biio.markers right for children or adolescents?

biio. has a dedicated child and adolescent team for young people with complex overlapping concerns. Be sure to select the Child & Adolescent Pathway to see only the practitioners with paediatric experience.

If you are a patient at biio. yourself and booking on behalf of a child, please use a unique email address - different to the address used for your patient portal account - to preserve your login credentials.

Appointment details
Who runs the assessment?

A biio. clinician trained in complex invisible illness will conduct your assessment. The specific clinician may depend on your appointment type and clinical needs.

For connective tissue biio.markers, physiotherapists typically take the lead. For hormonal biio.markers, experienced nurse practitioners step forward. For dysautonomia, you may see a exercise physiologist or physiotherapist, just depending on your availability.

All clinicians performing biio.markers assessments have undertaken additional training - under the tutorage of biio.'s leadership - so you can rest assured, you'll be in excellent hands.

How long is the appointment?

biio.markers appointments are available in 60-minute, 90-minute and 120-minute formats. The hormonal assessment is always 60 minutes. Longer appointments are used when the presentation is more complex or requires more dedicated assessment time.

What happens during the appointment?

Your clinician will review your health history, current symptoms, relevant body systems, past investigations, medications, previous treatment attempts, functional patterns and current goals. Where clinically appropriate, they may also conduct targeted functional testing or pathway-specific screening. The appointment is designed to answer: what is known, what remains uncertain, what should happen next, and who is responsible for that next step.

Will I have to repeat my whole story again at every appointment?

That is what biio. is trying to reduce. Your biio.markers assessment becomes your foundational record in biio.graphy. The next clinician should be able to see what was gathered, what was decided, what remains uncertain and what needs to happen next. You may still need to clarify details as care continues, but you should not be left carrying the whole system by yourself.

Reports and documentation
Will I receive a written report?

Yes. biio.markers produces a written clinical report. The report summarises your health history, findings, working clinical picture, management plan, recommended care team, possible external supports or referrals, review points and safety parameters.

How long does the report take?

Report timing depends on operational capacity and the complexity of the material your clinician needs to review. If you need the report by a specific date, tell us before booking. This matters especially for NDIS, DSP, insurance, legal, school, university, workplace or specialist referral purposes.

Can I use the report for NDIS, DSP, insurance, school, university or workplace support?

Your report may help document your clinical picture, functional impact, recommended supports and next steps. However, external organisations may require specific forms, wording, evidence, functional capacity assessments or reports from particular practitioner types. biio. cannot guarantee that an external organisation will accept a biio.markers report for a specific administrative purpose. If documentation is the main reason you are booking, contact us first. We can help you decide whether biio.markers is the right appointment or whether another assessment type may be needed.

Can my GP or specialist receive the report?

Yes. Your report can be shared with referring clinicians or external providers where you consent and where sharing is appropriate.

Diagnosis and clinical scope
Will I receive a diagnosis?

Sometimes the assessment can clarify whether your presentation aligns with diagnostic criteria or whether a particular diagnosis should be investigated. Sometimes the honest answer is that more information, a specific clinician, a formal pathway or an external specialist is needed before diagnosis can be confirmed. Your clinician will not perform certainty for effect. The report should state what is known, what is not yet known, what is being recommended and who is responsible for the next step.

Can biio. diagnose EDS or HSD?

Some connective-tissue questions require structured diagnostic work. biio.markers may identify whether that kind of pathway or specialist review is appropriate. A formal diagnosis may require specific clinical criteria, examination, exclusion of differentials, medical specialist input or genetic escalation where indicated. If your main reason for booking is formal EDS/HSD documentation for NDIS, insurance, legal or administrative purposes, contact us before booking so we can help you choose the right pathway.

Can genetic testing confirm EDS?

It depends on the type of EDS being considered. Genetic testing can be relevant for some rare EDS subtypes and other heritable connective-tissue disorders. It cannot currently confirm or rule out hypermobile EDS, because hEDS does not have an identified genetic marker and is diagnosed clinically. If your history suggests a rare or heritable connective-tissue disorder, your clinician may recommend genetic counselling, genetic testing or specialist referral.

Will this repeat tests I have already done?

Not unless there is a clinical reason. biio.markers starts with what already exists: your reports, tests, history and lived patterns. The point is not to duplicate investigations. The point is to understand what has already been found, what it does not explain and what needs review next.

Can biio. order tests?

Your clinician may recommend investigations where clinically appropriate. Whether tests are ordered directly through biio., requested through your GP, or referred to another specialist depends on the test, practitioner scope, safety, funding and clinical need.

Costs and funding
Medicare rebates

Many patients with chronic or complex health conditions may be eligible for a Chronic Disease Management Plan. For eligible patients, Medicare provide rebates on up to five individual allied health services per calendar year.

When seeking a care plan from your GP, simply ask them to address it to Biio, rather than allocate it to a specific clinician. This will enable you flexibility to see whichever practitioner is most appropriate and available soonest.

Bring your referral letter to your appointment or upload it before your session so our team can advise what can be claimed.

Can I claim Medicare?

Many patients with chronic or complex health conditions may be eligible for a Chronic Disease Management Plan. For eligible patients, Medicare provide rebates on up to five individual allied health services per calendar year.

When seeking a care plan from your GP, simply ask them to address it to Biio, rather than allocate it to a specific clinician. This will enable you flexibility to see whichever practitioner is most appropriate and available soonest.

Bring your referral letter to your appointment or upload it before your session so our team can advise what can be claimed.

What is a CDMP or GP chronic condition management plan?

This is the Medicare pathway many patients use for chronic or complex health conditions. Your GP may call it a CDMP, EPC, care plan, GP Management Plan, Team Care Arrangement or GP Chronic Condition Management Plan. The terms have changed over time. Ask your GP whether you are eligible and whether biio. appointments can be included in your referral.

Can I use private health?

Private health rebates may apply depending on your fund, your level and type of cover.

Please check with your insurer before booking if rebate certainty is important to you.

Can I use NDIS funding?

biio. can work with self-managed and plan-managed NDIS participants where the service fits the person's plan, goals and funding categories.

NDIS funding rules are individual. biio. cannot guarantee that a plan manager, support coordinator or the NDIA will approve a claim.

If you need the assessment or report for NDIS purposes, tell us before booking. We can help you understand what the assessment can document, what it cannot decide, and whether another report type may be more appropriate.

Can I use DVA, workers compensation or motor vehicle accident insurance?

biio. accepts some third-party funding arrangements where the referral, approval and service type are appropriate from Western Australia only.

Eastern states patients under worker's compensation or motor accident claim may still access biio services, however you need to pay for your appointments and claim the accounts back from your insurer directly.

DVA patients may access biiomarkers assessment with full cover. DVA cover is not available for medical services at biio.

Please contact us before booking if your appointment will be funded through DVA, workers compensation, motor vehicle accident insurance or another insurer. It is better to clarify approval requirements before you attend.

Telehealth and preparation
Can I do this by telehealth?

Yes. biio. is a digital-first practice caring for people with invisible illness Australia-wide. biio.markers assessments are available by secure telehealth. Telehealth is often appropriate for people with fatigue, pain, dysautonomia, sensory sensitivities, mobility limitations or regional access barriers.

What do I need for telehealth?

You will need a private space, stable internet, a device with camera and audio, your documents nearby, your medication and supplement list, and a blood pressure monitor or heart rate monitor if you are booking for dysautonomia, POTS or orthostatic symptoms and have been asked to have one available.

I do not have a blood pressure monitor. Can I still book?

Yes, but tell us before the appointment if dysautonomia, POTS or orthostatic testing is part of your concern. Your clinician can advise what is needed and whether the appointment can proceed fully without home monitoring equipment.

What should I bring?

Bring any reports, results, imaging, specialist letters, medication lists, previous care plans, diagnosis letters or documentation requests you have. Do not delay booking because your records are incomplete. Bring what you have.

Should I prepare a timeline?

A timeline can help, but it does not need to be perfect. Useful points include when symptoms began, major infections, injuries, pregnancies, surgeries, stressors or life events around changes, what has worsened or improved symptoms, what diagnoses or explanations you have been given, and what treatments helped, failed or caused harm.

After the assessment
What happens after my assessment?

You receive a report and next-step recommendations. Your clinician may recommend one or more biio. practitioners, a structured pathway, continuing care, external referral, further investigation or a review point.

Do I have to see every practitioner recommended?

No. Your care team is chosen with you. Your clinician should consider what you need clinically, but also what you have capacity for - financially, physically, cognitively and emotionally. A good plan is not just clinically interesting. It has to be usable.

What if I cannot afford the whole care plan?

Tell us. Your clinician can help prioritise what matters first. Care can often be sequenced. The assessment should make the next step clearer, not leave you with an impossible list.

Will my care be coordinated?

The purpose of biio.'s model is to reduce the burden of disconnected care. Your record, report and practitioner recommendations are designed so the next clinician can see what has already been gathered and why the next step matters.

What if biio. is not the right fit after assessment?

Then your clinician should tell you what kind of care, specialist, service or pathway is more appropriate. A mismatch should not mean dismissal. It should mean clearer routing.

Book your biio.markers assessment today

This isn't another referral—it's the beginning of integrated care that honours both your measurable biomarkers and your meaningful biography, creating a complete picture that matches the complexity of your lived experience.

Experience care that listens from Australia's premier invisible illness team

Available Australia-Wide
No Referral Required
mother & daughter happy together

Which biio.markers assessment is right for me?

Enter biio.markers guided by your most pressing questions. The assessment names where to start; it does not decide what care plan follows. You clinician will adapt your assessment dynamically based on your priorities at the time.

Universal biio.markers
If you're already diagnosed or not sure where to start.
60 min
Connective Tissue biio.markers
Hypermobility, suspected Ehlers-Danlos syndrome.
90 min
Dysautonomia biio.markers
POTS, orthostatic intolerance, fatigue or autonomic symptoms.
90 min
Immune biio.markers
Long COVID, ME/CFS, PEMs, post-viral decline or MCAS concerns.
90 min
Neurodivergent Health biio.markers
ADHD, autism, AuDHD, sensory processing differences, executive function issues, neurodivergent burnout, ARFID or developmental complexity.
60 min
Hormonal biio.markers
Perimenopause, menopause, menstrual changes, pelvic pain, thyroid concerns, testosterone concerns, sleep or circadian rhythm disruption.
60 min
Multi-diagnostic biio.markers
You have clear features across more than one major route, especially dysautonomia and/or immune or post-viral features alongside connective tissue features.
120 min
Universal biio.markers

Choose this if you have multiple diagnoses, you are not sure where to start, or you need a broad first assessment across systems.

This assessment covers:

  • your full health history;
  • the main symptoms and systems currently affecting you;
  • existing diagnoses, suspected diagnoses and previous investigations;
  • medications, supplements and previous treatment attempts;
  • what remains unclear;
  • which therapies, clinicians or clinical pathways may be most appropriate next.

This is often the best choice when the first question is simply: "Where do I start?"

Connective Tissue / Hypermobility biio.markers

Choose this if your main question is connective tissue, hypermobility, EDS, HSD or another heritable connective tissue disorder.

This assessment may cover:

  • review against hEDS diagnostic criteria where clinically appropriate;
  • hypermobility history and current joint behaviour;
  • subluxations, dislocations, sprains, instability, soft tissue injury or chronic musculoskeletal pain;
  • skin, tissue fragility, bruising, scarring or wound-healing features;
  • family history that may suggest EDS or another heritable connective tissue disorder;
  • screening for features that may suggest a rare EDS subtype or another HCTD, such as Marfan syndrome, Loeys-Dietz syndrome or another heritable connective tissue disorder;
  • whether genetic counselling, genetic testing, rheumatology review or another specialist referral may be needed;
  • how connective tissue findings may relate to autonomic, gastrointestinal, immune, fatigue, pain, hormonal or neurodivergent features.

This route is not only for people who already know they have EDS. It is for people whose presentation raises a connective-tissue question that needs structured review.

Diagnostic limitations: This assessment can help identify whether your presentation aligns with hEDS/HSD criteria or whether rare subtype screening or specialist escalation is needed. It does not constitute a formal diagnosis in itself. Only medical practitioners can provide formal diagnoses.

Dysautonomia biio.markers

Choose this if your main question is autonomic function: what happens when your body has to regulate heart rate, blood pressure, temperature, digestion, exertion, recovery or upright posture.

This assessment may cover:

  • symptoms of POTS, orthostatic intolerance, orthostatic hypotension, inappropriate sinus tachycardia or related autonomic patterns;
  • a NASA Lean Test protocol or orthostatic observations where clinically appropriate;
  • review of heart rate, blood pressure and symptom changes with posture;
  • heat intolerance, exercise intolerance, post-exertional worsening, presyncope, faintness or palpitations;
  • clinical review of POTS subtypes, patterns or phenotypes so care can be directed more precisely;
  • contributing features such as connective tissue variation, immune activation, deconditioning, post-viral change, trauma physiology, hydration, salt tolerance, sleep, medication effects or hormonal interaction;
  • what needs GP, cardiology, neurology or other specialist review.

For telehealth assessments, you may be asked to have a blood pressure monitor or heart rate monitor available. Your clinician will guide you. Do not perform testing before the appointment unless you have been specifically asked to.

Immune / Post-Viral biio.markers

Choose this if your health changed after infection, immune activation, vaccine response, inflammatory flare or an illness you never fully recovered from.

This assessment may cover:

  • post-viral features and the timeline of decline;
  • Long COVID, ME/CFS, chronic fatigue presentations or post-infectious change;
  • PEMs — worsening after physical, cognitive, emotional or sensory exertion;
  • orthostatic intolerance, dizziness, tachycardia or dysautonomia features that may be part of the picture;
  • MCAS or mast-cell-pattern symptoms where relevant;
  • immune flares, allergies, food reactions, inflammatory features or infection-triggered worsening;
  • sleep, pain, cognitive load, sensory sensitivity, gastrointestinal symptoms and functional capacity;
  • whether NASA Lean testing or orthostatic observations are appropriate based on your presentation;
  • what needs GP, immunology, cardiology, neurology, respiratory, infectious disease or other specialist review.

This assessment is especially useful when several explanations are possible and the next step depends on distinguishing them carefully.

Neurodivergence biio.markers

Choose this if neurodivergence is part of your health picture, or you suspect it may be.

This assessment may cover:

  • ADHD, autism, AuDHD or suspected neurodivergence as part of the health picture;
  • sensory processing differences, sensory overwhelm, shutdown patterns or care environments that make symptoms harder to manage;
  • executive function, attention, task initiation, transitions, planning and daily capacity;
  • developmental history and how early patterns may still affect health, function, sleep, eating, movement, pain, fatigue or care access;
  • neurodivergent burnout and loss of function;
  • ARFID, restricted eating, interoception, appetite cues or food-related sensory barriers;
  • communication preferences and appointment accessibility;
  • school, work, study, parenting or daily-living capacity;
  • medication history where relevant;
  • overlap with pain, hypermobility, dysautonomia, gastrointestinal symptoms, immune activation, sleep disruption or hormonal changes;
  • what support may be needed from psychology, occupational therapy, dietetics, psychiatry, GP, paediatrics, school, work or other services.

This route should not make you feel reduced to a label or a behaviour checklist. The clinical question is how neurodevelopmental patterns, sensory load, executive capacity and body-system symptoms may be affecting function and care.

Hormonal biio.markers

Choose this if the main question is hormonal, menstrual, pelvic, thyroid, testosterone, perimenopause, menopause, sleep or circadian rhythm change.

This assessment may cover:

  • perimenopause or menopause symptoms;
  • menstrual cycle changes, PMS/PMDD-type patterns or cycle-linked symptom flares;
  • pelvic pain, endometriosis history or reproductive health concerns where relevant;
  • thyroid concerns or symptoms that may need pathology review;
  • low testosterone or androgen-related concerns;
  • HPA-axis stress physiology, sleep disruption, circadian rhythm change or fatigue patterns;
  • how hormonal changes may interact with dysautonomia, migraine, pain, mood, immune symptoms, connective tissue symptoms or neurodivergent capacity;
  • what pathology is needed before the follow-up;
  • what should be reviewed with your GP, gynaecologist, endocrinologist or other specialist where needed.

The hormonal route is structured differently from the longer assessments. The initial appointment identifies the clinical question and customises the pathology request. Your pathology is then reviewed in a follow-up appointment, where your clinician can interpret the results in context and discuss next steps.

Multi-diagnostic biio.markers

Choose this if your presentation clearly crosses more than one major route and a shorter assessment would likely split the picture too early.

This assessment is especially useful when you have:

  • dysautonomia or POTS features and connective tissue features;
  • immune or post-viral symptoms and connective tissue features;
  • orthostatic intolerance, PEM/PESE, MCAS-type symptoms and hypermobility;
  • multiple partial diagnoses that do not explain the whole pattern;
  • a history where the main question is not one condition, but how several systems are interacting;
  • significant documentation needs where the report must organise several clinical questions clearly.

This assessment may cover:

  • connective tissue pattern review;
  • dysautonomia screening and orthostatic observations where clinically appropriate;
  • immune or post-viral features, PEM/PESE and MCAS-pattern review;
  • relevant neurodivergent, hormonal, gastrointestinal, sleep, pain or fatigue factors where they affect the main clinical question;
  • existing investigations and what they do or do not explain;
  • which clinical pathway, practitioner or external specialist should take responsibility for each next step.

Fees & rebates

Financial clarity is part of good care. You should know what you are booking before you book it.

60 min

$240

60-minute
Signature biio.markers assessment — for diagnosed patients or those who are unsure where to begin.
90 min

$320

90-minute
Complex or specialised, include Connective Tissue, Dysautonomia & Immune biio.markers.
120 min

$400

120-minute
Comprehensive multidiagnostic assessment
Medicare rebates

Many patients with chronic or complex health conditions may be eligible for a Chronic Disease Management Plan. For eligible patients, Medicare provide rebates on up to five individual allied health services per calendar year.

When seeking a care plan from your GP, simply ask them to address it to Biio, rather than allocate it to a specific clinician. This will enable you flexibility to see whichever practitioner is most appropriate and available soonest.

Bring your referral letter to your appointment or upload it before your session so our team can advise what can be claimed.

Private health cover

Private health rebates may apply depending on your fund, your level and type of cover.

Please check with your insurer before booking if rebate certainty is important to you.

NDIS

biio. can work with self-managed and plan-managed NDIS participants where the service fits the person's plan, goals and funding categories.

NDIS funding rules are individual. biio. cannot guarantee that a plan manager, support coordinator or the NDIA will approve a claim.

If you need the assessment or report for NDIS purposes, tell us before booking. We can help you understand what the assessment can document, what it cannot decide, and whether another report type may be more appropriate.

DVA, workers compensation and motor vehicle accident insurance

biio. accepts some third-party funding arrangements where the referral, approval and service type are appropriate from Western Australia only.

Eastern states patients under worker's compensation or motor accident claim may still access biio services, however you need to pay for your appointments and claim the accounts back from your insurer directly.

DVA patients may access biiomarkers assessment with full cover. DVA cover is not available for medical services at biio.

Please contact us before booking if your appointment will be funded through DVA, workers compensation, motor vehicle accident insurance or another insurer. It is better to clarify approval requirements before you attend.