Conditions · Beachside EP

Exercise Physiology for POTS & Dysautonomia

Postural Orthostatic Tachycardia Syndrome and Orthostatic Intolerance are poorly understood, often mismanaged conditions. We offer something rare: clinician-led exercise care from someone who has lived it.

Medicare, NDIS and DVA accepted No referral needed to start Clinician with lived experience in POTS

Exercise Physiologist at Beachside EP guiding a client through a POTS rehabilitation program
1 in 100
Australians estimated to be living with POTS, most of them undiagnosed or misdiagnosed
3-6 yrs
Average time to diagnosis for people with POTS, often dismissed as anxiety or deconditioning
First-line
Exercise rehabilitation is a primary treatment recommendation in international POTS guidelines
Lived XP
Our clinician Sierra has personal experience with Dysautonomia, POTS and Orthostatic Intolerance
From your Exercise physiologist
"I have lived with Dysautonomia myself. I know what it takes to manage these conditions day to day, and I know what good care looks like. That is what I bring to every person I work with."
Sierra Accredited Exercise Physiologist · Lived experience in Dysautonomia, POTS & Orthostatic Intolerance
What is it?

A real, physical condition. Not anxiety. Not laziness. Not just being unfit.

Postural Orthostatic Tachycardia Syndrome (POTS) is a form of dysautonomia, a dysfunction of the autonomic nervous system that regulates heart rate, blood pressure, digestion and many other automatic body functions.

In POTS, the body fails to properly regulate blood flow when you stand. Heart rate surges, blood pools in the lower body and the brain receives less oxygen than it needs. The result is a constellation of symptoms including racing heart, dizziness, brain fog, extreme fatigue and nausea that can make even basic daily activities feel impossible.

Orthostatic Intolerance (OI) is a broader term for conditions where symptoms worsen on standing and improve when lying down. Many people with POTS also experience overlapping OI. Both conditions are frequently dismissed, misdiagnosed as anxiety or panic disorder, and left untreated for years. That delay causes real harm. Getting the right support, sooner, changes outcomes.

Exercise Physiologist and client working on a graduated recumbent program for POTS
The Most Important Thing to Understand

Exercise is one of the most effective treatments for POTS, but the wrong kind of exercise can make things significantly worse.

This is not a condition where a standard exercise prescription applies. Upright exercise, high-intensity training and programmes that ignore orthostatic stress can trigger symptom flares, prolong recovery and erode the trust people with POTS have in exercise as a tool at all.

The research is clear: a carefully graduated, largely recumbent or semi-recumbent programme that progressively builds cardiovascular and postural tolerance is an evidence-based first-line treatment. The clinical skill is knowing exactly how to structure, progress and adapt that programme for your specific presentation, including on the days when your body simply will not comply. That is what we do.

Common misunderstandings

What people get wrong about POTS and exercise

People with POTS hear a lot of well-intentioned but unhelpful advice. Here is what the evidence actually says.

Myth

POTS is just deconditioning. Push through it and you will get better on your own.

Fact

While deconditioning can worsen POTS, the condition has distinct autonomic and sometimes structural causes. Unguided push-through exercise frequently causes post-exertional symptom flares and sets people back significantly.

Myth

If you cannot stand up properly, exercise is too dangerous to attempt.

Fact

Evidence-based POTS exercise begins in recumbent positions including rowing, swimming and cycling, specifically because it avoids orthostatic stress while building the cardiovascular base needed to tolerate upright activity over time.

Myth

POTS is a psychological condition. The symptoms are caused by anxiety.

Fact

POTS is a physiological disorder with measurable autonomic dysfunction. Anxiety is a common consequence of living with debilitating undiagnosed symptoms, not the cause. Appropriate physical treatment is the primary intervention.

Myth

Rest is the safest approach while waiting to see a specialist.

Fact

Prolonged rest accelerates cardiovascular deconditioning and worsens POTS symptoms over time. Even low-intensity recumbent activity, introduced carefully, is preferable to extended bed rest while awaiting specialist review.

What we do

A program built around your autonomic system, your symptoms and your life

Every POTS program at Beachside EP begins with a thorough assessment of your symptom profile, functional capacity and daily limitations. We design from there, not from a template.

Graduated recumbent exercise

We begin where your body is. Rowing machines, recumbent cycling and swimming-based programmes build cardiovascular fitness without triggering orthostatic symptoms. Upright activity is introduced gradually as tolerance improves.

Postural tolerance training

Progressive exposure to upright positions, managed carefully using heart rate monitoring and symptom response, helps retrain your autonomic nervous system's response to standing over time.

Strength and muscle pump work

Building lower limb and core strength improves the venous muscle pump, reducing blood pooling and supporting better blood return to the heart when upright.

Heart rate monitoring and load management

We monitor heart rate throughout every session and teach you to manage your own load using evidence-based heart rate targets for POTS. You leave each session knowing how to train safely between appointments.

Fatigue and post-exertional management

We understand pacing. For those with concurrent ME/CFS or post-exertional malaise, we structure programmes that build capacity without triggering crashes.

Breathwork and nervous system regulation

Breathing techniques that support parasympathetic activation help manage the acute symptom response and support autonomic regulation between exercise bouts.

Education and self-management tools

Understanding your condition changes how you manage it. We explain the physiology of POTS in plain language and give you practical strategies for fluid intake, salt loading, compression garments and activity pacing.

Coordination with your care team

We communicate regularly with your cardiologist, GP, neurologist or other treating clinicians. Written progress reports ensure your exercise programme is aligned with your broader medical management.

Who it is for

Who we see

POTS and dysautonomia present differently in every person. We work across the full spectrum.

·Diagnosed POTS ·Orthostatic Intolerance ·Hyperadrenergic POTS ·Neuropathic POTS ·Post-viral POTS including Long COVID ·Suspected dysautonomia awaiting diagnosis ·Hypermobile Ehlers-Danlos with POTS ·Mast Cell Activation Syndrome with POTS ·Adolescents and young adults with POTS ·POTS with concurrent ME/CFS ·POTS with anxiety or depression ·Post-surgical or post-hospitalisation dysautonomia

Not sure if this is you? You do not need a confirmed diagnosis to book. Many people we see are still in the process of being investigated. We assess your symptoms and function, not your paperwork.

Book an initial assessment
Why this matters to us

Care from someone who understands from the inside

Sierra is an Accredited Exercise Physiologist at Beachside EP with personal lived experience of Dysautonomia, including Postural Orthostatic Tachycardia Syndrome and Orthostatic Intolerance.

She knows first-hand the impact these conditions have, not just on the person living with them, but on the families around them. The exhaustion of unexplained symptoms. The frustration of being dismissed. The fear of exercise when your body has taught you that movement comes with consequences.

That lived experience shapes how she practises. Sierra brings deep compassion alongside her clinical training, meeting each person where they are and building programmes that are meaningful to that individual, not just clinically sound in a textbook sense. Her focus is long-term health outcomes that matter to the person in front of her.

Working with Sierra

  • Accredited Exercise Physiologist registered with ESSA
  • Lived experience in Dysautonomia, POTS and Orthostatic Intolerance
  • Evidence-based, individually tailored programming
  • Compassionate, unhurried clinical approach
  • Experienced with complex and overlapping presentations
  • Coordinated care with your existing medical team
Meet the full team
Your program

What to expect from your first appointment

We assess before we prescribe. Every POTS program is individual because every patient's symptom profile, triggers and goals are different.

1

Initial assessment

A thorough review of your symptom history, triggers, current medications and what daily life looks like for you right now. We assess your current functional capacity in positions your body can tolerate and identify your starting point. This takes 45 to 60 minutes.

2

Personalised program design

We build a programme around your specific POTS presentation, recumbent where needed, progressive always, and structured around what is meaningful to you. We explain the rationale for every choice so you understand what we are doing and why.

3

Supervised sessions with real-time monitoring

Sessions are supervised with heart rate monitoring and symptom tracking throughout. Your clinician adjusts intensity in real time based on your response. You also receive your programme via our exercise app so you can train between sessions with confidence.

4

Regular review and progression

We review your programme at regular intervals, progress loading as your tolerance improves and adapt quickly when symptoms fluctuate. Written reports are sent to your GP, cardiologist or neurologist after every review so your whole team stays aligned.

A note on pacing: We do not expect you to progress linearly. POTS fluctuates. Some weeks you will improve; others your body will need a different approach. We build that flexibility into every programme from the start, and we never penalise you for a difficult day.
Funding and rebates

Multiple ways to fund your POTS program

POTS and Dysautonomia qualify as chronic conditions under several funding pathways. In many cases your out-of-pocket cost per session is significantly reduced.

Medicare CDM Plan

Chronic Disease Management

Up to 5 subsidised allied health sessions per calendar year with an active CDM plan from your GP. POTS qualifies as a chronic condition.

$61.80 rebate per session

NDIS

Improved Health & Wellbeing

Exercise Physiology is funded under the Improved Health and Wellbeing support category for self-managed and plan-managed NDIS participants.

Self and Plan Managed

DVA

Gold and White Card

DVA Gold Card holders have all clinically necessary Exercise Physiology sessions covered with no gap fee.

No gap fee (Gold Card)

Private Health Insurance

Extras Cover

Most extras policies cover Exercise Physiology. Check your fund for your annual limit and rebate amount.

Varies by fund

WorkCover / TAC

Injury and Illness Support

WorkCover and TAC funding can apply where POTS or dysautonomia is linked to a workplace injury or transport accident.

Case managed

Self-funded

No Referral Needed

Book directly and pay privately. No GP visit or referral is required to get started. We will guide you on rebate options at your first appointment.

No referral required

Funding and payments we accept
Medicare CDM NDIS DVA Gold Card DVA White Card WorkCover TAC Private Health Insurance Self-funded
Common questions

POTS program FAQs

Is exercise safe for someone with POTS? +
Yes, when it is prescribed correctly. Unguided or inappropriate exercise can trigger significant symptom flares in POTS, which is why so many people have had bad experiences with exercise in the past. Evidence-based POTS exercise protocols begin with recumbent or semi-recumbent activity to avoid orthostatic stress, then progress upright tolerance very gradually. Our clinician Sierra has both the clinical training and personal lived experience to design programmes that are genuinely safe and effective for POTS.
I have had terrible experiences with exercise before. Will this be different? +
Very likely yes. Most bad exercise experiences in POTS come from programmes that were not designed with your autonomic dysfunction in mind, well-intentioned advice from people who did not fully understand the condition. We start from where your body actually is, not where it theoretically should be. We take post-exertional response seriously and we do not push you past your physiological limits. Many of our POTS clients have found this to be the first exercise experience they have had that did not leave them worse off.
I do not have a formal POTS diagnosis yet. Can I still book? +
Yes. You do not need a confirmed diagnosis to start. Many people we see are still in the process of being investigated, waiting for a tilt table test, or have been told they have symptoms consistent with POTS but are yet to see a specialist. We assess your symptom profile and functional capacity and build from there. We can also write a letter supporting a referral to a cardiologist or autonomic neurologist if that would help your diagnostic pathway.
Do I need a referral to book? +
No. You can book directly and be seen privately without any referral. If you have a Medicare Chronic Disease Management plan from your GP that includes Exercise Physiology, bring it to your first appointment and we will process your $61.80 Medicare rebate on the spot. If you do not have one yet and think you might qualify, we can provide a letter to support your GP in setting one up.
I also have hEDS, MCAS, Long COVID or ME/CFS. Can you still help? +
Yes. POTS frequently presents alongside Hypermobile Ehlers-Danlos Syndrome, Mast Cell Activation Syndrome, Long COVID and ME/CFS. These overlapping conditions add complexity to exercise prescription but do not make it impossible. We are experienced with these presentations and take an individualised approach to every programme. Post-exertional malaise, hypermobility-related joint instability and mast cell triggers are all factored into how we structure your sessions.
Can I attend via telehealth? +
Yes. Telehealth appointments are available for review sessions, programme updates and education consultations. For initial assessments we generally recommend attending in person where possible so we can properly assess your postural response and movement. We will advise you on the best option for your situation at the time of booking.
What does a typical first appointment involve? +
Your first appointment takes 45 to 60 minutes. We will review your symptom history, triggers, current medications and what a typical day looks like for you. We will assess your current functional capacity in positions your body can manage, take relevant measurements and talk through your goals. At the end of the session we will outline a programme structure and schedule your next appointment.
Beachside EP · Mordialloc

You deserve care from someone who gets it.

Book your initial assessment with Sierra. We will start where you are, move at your pace and build a program around what matters to you.

Takes 60 seconds No referral needed to start Medicare, NDIS, DVA accepted Clinician with lived experience in POTS

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