Chronically Uncensored
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Diploma In Counselling and community Services
Personal journey Blog, living with Ankylosing spondylitis, Graves, & Fibro đȘ đ
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02/09/2026
đ 1000 SESSIONS DOWN FOR SAMMY!!đ
From our old Rumbles program, to general boxing classes, to STRONG â Sammy has shown up for every single one, and shown up for herself every time. She's the one checking in on you mid-set (sometimes she can't even wait till the rest period đ), always ready with a chat and a laugh no matter how heavy the bar is.
1000 sessions of turning up, getting stronger, and making SkyBox feel like home. đ€
Here's to the next 1000!! đ
02/09/2026
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24/08/2026
Hiya friends if you have ever wanted to try lifting in a fun and supportive space then this is the perfect opportunity. Who's joining me ?
Last Chance to Join She Lifts Registrations close 27 August.
23/08/2026
The house might look messy to someone walking in, but to me it reflects a body fighting just to keep up. itâs the energy I know it will drain from me. Laundry piling up isnât a sign of neglect, itâs the lifting, bending, carrying, and folding that I have to measure carefully against whatever strength I have left.
What others interpret as a lack of effort is actually the exhaustion that comes from doing tasks most people never have to think twice about. This isnât laziness or avoidance. Itâs the daily negotiation between my responsibilities and what my body can realistically handle while living with chronic
This is me choosing what my body can handle today.
Because with chronic illness, even the simplest tasks can feel like climbing a mountain with no summit in sight.
The Comments That Cut Deeper Than People Realise
âYou should apply for NDIS, you definitely qualify.â
âYou really need the help.â
"You need to slow down."
I hear these comments often. And people mean well. They see the struggle. They see the exhaustion. They see the impact on my mobility, my cognition, my pain levels, my fatigue.
What they donât see is the part that Iâm already on my third attempt for NDIS access.
Two tries.
Two rejections.
And one reason
I havenât done enough to âcureâ a degenerative, progressive disease that has no cure.
Imagine being told youâre not disabled enough while living in a body that fails.
Imagine having to prove your suffering to people who donât understand the complexity of chronic pain, mobility loss, cognitive shutdowns, and chronic fatigue.
Itâs dehumanising.
Itâs exhausting.
And itâs a battle I never asked for.
The Good Days, The Bad Days, and The Judgement in Between
People see me on a good day and think:
âShe isnât that sick.â
People see me on a bad day and think:
âShe was fine yesterday, she must be faking.â
People tell me:
âYou needs to slow down.â
What they donât see are the days I do slow down, because I physically cannot clean, drive, exercise, or function.
They donât see the 15âhour reset sleeps my body forces on me.
They donât see the cognitive shutdowns, the slurred speech, the shaking legs, the moments where I canât walk through a supermarket without my body collapsing, they don't see the immense pressure my condition puts on my friendships, my family, and my Girls.
They donât see the reality that one day, my ability to try new things, work, or support my girls in their incredible journeys may be taken away, or look very different.
Good days donât erase bad days.
Bad days donât erase good days.
Both are real.
The Anger, The Hurt, and the Reminders I Give Myself.
I often find myself full of anger, hurt, and disappointment amd assumptions, not just at the system, but at the people who abuse the supports Iâm fighting so hard to access.
Itâs painful to watch others misuse what I desperately need.
But I have to remember and check myself, that I cannot assume everyone is abusing the system, I have to be mindful not to judge people.
Everyone has their own path with disability, chronic illness, and mental health struggles.
Everyoneâs story is different.
Everyoneâs challenges are valid.
The Truth Behind the Mess
Sometimes my house is messy.
Sometimes the dishes sit.
Sometimes the laundry waits.
Sometimes the floor doesnât get a vacume and mop.
But every single day, I am doing the best I can with the body I have.
And that deserves understanding, not judgement.
Compassion, not assumptions.
Support, not dismissal.
Because behind the mess is a person fighting a battle most people never have to think twice about.
19/08/2026
As a business, you need clients.
Your clients matter!
Without your clients, you wouldnât exist
As such, when a client goes through a difficult time, sometimes itâs compassionate and considerate to reach out and offer assistance in any way - to help make the process less stressful and comfortable for them and their family
Itâs easy to reach out and say âwe care, we are hereâ
9 times out of 10, a client isnât just someone you grow to know, they become FAMILY.
16/08/2026
Runway to the crown Fashion show hosted by Turning Point Models Australia at Batavia Brewing Saturday the 15th August.
Doors open at 4:30 pm.
Purchase your ticket today and help support three amazing local Geraldton ladies Represent Australia in the 2026 Heritage Pageants Thailand in November. We are extremely blessed to have local businesses and entertainment come together to showcase their fashion, art, Photography, dance, music and talents.
A massive thank you to our sponsors we truly appreciate all support.
On-Point Photography WA
Batavia Brewing
Meraki Fashion & Style
Ivy Vibe
lil Suga clothing
Leigh Clifford and Ratna Clifford
https://www.trybooking.com/events/landing/1608045
Chronically Uncensored
Diploma In Counselling and community Services
Personal journey Blog, living with Ankylosing spondylitis, Graves, & Fibro đȘ đ
https://acca.member365.org/mms/api/memberbadge/y3sQbluFxAS_K5ZrpajoOw/4TmtReTeal_p4BVlGbmThA/
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