Jacqui Main Exercise Physiologist at Dizzy heds & Co.

Jacqui Main Exercise Physiologist at Dizzy heds & Co. I advocate & educate those living with EDS, HSD, Dysautonomia, POTS, ME/CFS, & Chronic Pain

Due to a very frustrating loophole, Exercise Physiologists are required to charge GST that other Allied Health professio...
03/06/2026

Due to a very frustrating loophole, Exercise Physiologists are required to charge GST that other Allied Health professions are exempt from. In a system where we are often undervalued and not funded to the same level as our Allied Health counterparts, despite studying just as hard for just as long, we also have to hand over 10% of our hard earned, as GST.

But this can impact you too as some clinics do need to therefore add GST to services.

If you know and love, and/or have benefited from working with an Accredited Exercise Physiologist, please help us out by signing this petition to try and bring us into alignment with our peers. Let's Axe The Tax.

Axe the tax on health – sign the petition to remove GST from exercise physiology services  Australians shouldn’t be paying tax on essential healthcare. 

A very important post to read - I love it because it focuses on 'protecting your energy and capacity' around all the pol...
14/05/2026

A very important post to read - I love it because it focuses on 'protecting your energy and capacity' around all the political s**t that is going on.

https://www.facebook.com/share/p/1CkkQFhngs/

Hey fam 💛

A gentle suggestion: you do not need to watch Mark Butler introduce the new NDIS bill today.

You just don't. :)

Please protect your capacity.

Political messaging can be intentionally provocative, and our community needs its energy for the advocacy ahead.

We’ll share a clear plain English summary of the bill tonight after 5pm, so nobody feels pressured to watch in real time.

If you want direct 'access without the stress':

Download the draft bill from the Parliament website, pop it into ChatGPT, and ask for a neutral two-paragraph plain English summary. Ask it to check for accuracy before briefing you.

Stay informed *without* absorbing the rhetoric. Just take it out of the picture altogether, because it hurts and you can be effective without hearing it at all.

Negative campaigning is a real, established political strategy.

What is negative campaigning?

It is a campaign strategy used globally that tactically deploys fear, conflict, urgency, emotionally loaded framing, and provocation to destabilise opponents, drain their energy, fracture communities, and control the debate.

Political strategists actively design campaigns around these tactics because they can be effective at creating panic, distraction, and reactive behaviour instead of organised action. They use it to weaken activism.

For neurodivergent communities, that really matters.

Many of us experience differences in emotional regulation, threat processing, justice sensitivity, communication, or stress response. That is not a weakness. It is simply relevant context we can use to our advantage.

A strategy built around outrage, panic, confusion, or provocation can hit this community especially hard. They absolutely know this.

The predictable result looks like:

• panic sharing
• doom spirals
• community infighting
• impulsive reactions
• burnout before the real political fight begins

So: we do not hand over that power. We get strategic.

Come back to facts, daily.

"Checking the facts" is one of our best strategies right now.

So, what are the facts today?

The bill has not passed. We have time.

It still has to go through the Senate.

The Government does not have the same Senate position it had during the last major NDIS legislation fight.

The Senate is not a rubber stamp.

The Senate are low key crankypants at the ALP most days and the cross bench is strong.

We are well connected to the cross bench, and so are our union allies.

So, our suggested strategy:

• check facts before sharing

• separate announcements from actual law

• step away from deliberately activating content

• do not let infighting drain capacity

• use trusted information channels

• stay connected, co regulate

• make a calm plan whenever you can rather than reacting online, even if you just increase that by 10 percent that leads to less "social transmission" of panic. Help your ND fam!

• act strategically. Always.

This is not silence.

It is not passivity.

It is strategy :)

A frightened, dysregulated community is waaaay easier to exhaust.

A calm, connected, informed, organised neurodivergent community is much, much harder to defeat.

Tune out today. Laugh at the circus. Pat a dog. Let DPOs do some of the heavy lifting for a few hours 🐾 We got you!

People’s fear, anger and grief right now are understandable. This is, totally, not abstract politics for our community. It is about our children, our safety, our independence, our families, and our futures. We get that.

But we are stronger when we take active steps to protect both our capacity and safety - and each other.

Put down the rectangle of doom and take care of your precious heart. Be with your gorgeous kids. Know the community are working, and we've got this.

Look at this beautiful photo below and remember every incredible thing we've achieved together as a movement - and rest.

We are getting ourselves organised with strategy and will be in touch with members and the community soon to plan our push back to this bill. There's plenty we can do! Heaps n heaps!

Love to you all x

❤️❤️❤️❤️

13/05/2026
This clinic has personally helped my little boy since he was 18 months old and I couldn't be more grateful for this amaz...
12/05/2026

This clinic has personally helped my little boy since he was 18 months old and I couldn't be more grateful for this amazing clinic.

For Hypermobility & EDS Awareness Month this May, Ocean Kids Health, Ocean Kids Health in Seaford is offering paediatric hypermobility screening sessions, and we’d love your support in identifying children who may benefit. Please see our attached flyer to post in your clinic / share with your team and families.

Who is it for?
• Children (4–16 yrs) who are:
• Very flexible / “double-jointed”
• Experiencing pain or frequent injuries
• Having challenges with coordination, stamina, or posture
• Having difficulties with strength and balance
• Participation challenges e.g. keeping up with peers

What’s included:
• 20-minute physiotherapy screening
• Brief assessment + discussion of concerns
• Individualised guidance and next steps

Cost & Contribution:
• $50 per screening
• We will donate 50% of proceeds to The Ehlers-Danlos Society to support research and advocacy!

Further info and resources via The Ehlers-Danlos Society Website.

Screening Spots are limited throughout May, so please feel free to refer directly or share with families who may benefit.

We’re also running a light-hearted community “Walk & Roll Challenge” alongside this initiative to build awareness, support healthy activities and support fundraising efforts. Head to our socials to find out more!

Thanks for helping us support early identification of hypermobility and care in our community.

We provide evidence-based physical therapy for babies & children with motor delays, movement difficulties, injuries & childhood conditions. Book online!

10/05/2026
13/04/2026
18/03/2026

Address

Melbourne, VIC
3192

Opening Hours

Tuesday 10am - 2:30pm
Wednesday 10am - 3:30pm
Friday 9:30am - 1:30pm

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