Fibro Fighters

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Fibro Fighters My name is Rochelle and I was diagnosed with FMS in 2012 but have had symptoms since I was a child.

This group is a place for anyone who would like to vent or just get some support with their FMS. This is just simply a place to come on in and vent and feel free to voice how you are feeling, this is not just for invisible illnesses, it is for anyone who wishes to be apart of this group. Now a little about me just so you all know :) I was diagnosed by a physical therapist in 2009 with Fm and never did much research on it and then once I started getting worse I started looking for answers and I finally went to see a Rhumatologist in early 2012 and he stated that yes I do have FM and it is a pretty moderate case, I have also been diagnosed with Ankylosing Spondylitis, and Osteoarthritis.

09/02/2026
09/01/2026
08/11/2026

💜FIBRO & ME💜

🌻20 THINGS WE PRETEND DON’T HURT🌻

(But People With Fibromyalgia Know They Do!)

One of the hardest parts of living with fibromyalgia is that so many painful moments look completely ordinary to everyone else.

People see us getting on with life…

They don’t see the pain hiding behind the smile.

These are the little things many of us quietly push through every single day.

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20 THINGS WE PRETEND DON’T HURT

1. Getting out of bed in the morning.

2. Standing long enough to have a shower.

3. Brushing or washing our hair.

4. Carrying the shopping into the house.

5. Walking around the supermarket.

6. Sitting in one position for too long.

7. Standing up after sitting for a while.

8. Going up and down the stairs.

9. Reaching into a cupboard.

10. Holding a conversation when fibro fog kicks in.

11. Smiling when we’re actually having a flare.

12. Wearing certain clothes because our skin hurts.

13. Opening jars or bottles.

14. Sleeping… and somehow waking up even more exhausted.

15. Hugging people when our body feels bruised.

16. Driving for more than a short distance.

17. Pretending we’re listening when our brain has completely wandered off.

18. Saying “I’m fine” because it’s easier than explaining everything.

19. Watching everyone else keep going while our body says, “Enough.”

20. Missing the person we used to be.

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THE TRUTH IS…

Many of us have become experts at hiding our pain.

Not because we want sympathy.

But because we’re tired of hearing:

“You seemed fine yesterday.”

“You don’t look ill.”

“Maybe you’re just tired.”

So we smile.

We carry on.

We push through.

And most people never realise how much effort that takes.

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YOU AREN’T WEAK

If you recognised yourself in this list, please remember this:

You aren’t lazy.

You aren’t dramatic.

And you certainly aren’t weak.

Every day you keep going despite pain, fatigue and fibro fog is a victory that many people never get to see.

That quiet strength deserves to be recognised.

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THE BOTTOM LINE

The smallest tasks can sometimes require the greatest courage.

What looks ordinary on the outside can feel like climbing a mountain on the inside.

So if someone with fibromyalgia says they’re having a difficult day…

Believe them.

Because chances are they’ve already pushed through twenty things that hurt before breakfast.

💜 DISCUSSION QUESTION

Which one on this list made you think…

“That’s me!”

Or what would you add as Number 21?

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07/28/2026

Dizziness, balance problems, and falls during fibromyalgia flare-ups are more common than many people realize. 💜😣🌀

Fibromyalgia is not only about widespread pain. This chronic illness can also affect energy, sleep, thinking, movement, sensory processing, and stability. During a flare-up, the body may feel weak, heavy, foggy, unsteady, and disconnected from normal coordination.

Many people with fibromyalgia describe feeling dizzy, lightheaded, off-balance, wobbly, or afraid they might fall. This can happen because the nervous system is already overloaded. When pain signals are amplified, the brain may struggle to process body position, movement, balance, and sensory information smoothly.

Fatigue can make this worse. When the body is exhausted, muscles may feel weaker, reactions may slow down, and walking may require more effort. Brain fog can also affect focus and coordination, making stairs, crowded places, uneven floors, or quick movements feel risky.

Some people may also experience dizziness when standing up, changing position, overheating, missing sleep, feeling anxious, or pushing through too much activity. During flare-ups, the body may become more sensitive to light, noise, motion, and temperature changes, which can make balance feel even harder to control.

Pain itself can change the way a person walks. If the back, hips, knees, legs, or feet hurt, the body may shift weight differently, walk slower, or move stiffly. This can increase the risk of stumbling or losing balance.

Falls should always be taken seriously. Dizziness or balance problems can also come from low blood pressure, dehydration, inner ear problems, migraine, anemia, medication side effects, nerve issues, heart problems, or neurological conditions. Fainting, chest pain, weakness on one side, slurred speech, severe headache, injury, or repeated falls need urgent medical attention.

If fibromyalgia makes you feel dizzy or unstable during flare-ups, you are not imagining it. Your body may be overwhelmed, your symptoms are real, and your safety matters.

07/11/2026

💜FIBRO & ME💜

🔥WHO ELSE HAS DECIDED THEY WON’T EXPLAINING THINGS TO ANYONE ELSE?
NEVER WILL I WASTE MY TIME EXPLAINING TO PEOPLE WHO REALLY DON’T WANT TO EVEN TRY AND UNDERSTAND🔥

07/11/2026

💜 FIBRO & ME 💜

🔥 THE HABITS FIBROMYALGIA HAS GIVEN ME 🔥

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Fibromyalgia changes more than your body.

It changes the little things you do every single day.

Some habits are helpful.

Some are frustrating.

And some have become so normal that you don’t even realise you’re doing them anymore.

If you live with Fibromyalgia, I bet you’ll recognise quite a few of these.

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I automatically look for the nearest chair wherever I go.

Not because I’m lazy…

Because I know I might need it before anyone else does.

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I think twice before saying “yes” to anything.

Not because I don’t want to.

Because my body gets the final say.

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I pace everything.

Housework.

Shopping.

Cooking.

Even having a shower.

I’ve learnt the hard way that doing too much today usually steals tomorrow.

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I check the weather far more than I ever used to.

Because I know a change in temperature or pressure might mean a flare is on its way.

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I carry pain relief, water, snacks and anything else I might need…

Just in case.

My bag has become a little emergency survival kit.

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I celebrate the smallest victories.

Getting dressed.

Cooking dinner.

Walking a little further.

Changing the bedding.

Things that once seemed ordinary now feel like achievements.

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I’ve become an expert at saying…

“I’ll see how I feel.”

Because making promises my body might break has become too painful.

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I rest before I’m exhausted.

At least…

I try to.

I’ve learnt that waiting until I completely crash usually ends badly.

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I mentally calculate everything.

How far is the walk?

Are there stairs?

Where are the toilets?

Will there be somewhere to sit?

How much energy will this cost me?

Healthy people rarely have to think this way.

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I smile more than people realise.

Not because I’m pain free.

But because I’ve become very good at hiding how I really feel.

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Fibromyalgia has changed my habits.

But it has also taught me something important.

To appreciate the good days.

To be kinder to myself.

To stop comparing my life to other people’s.

And to celebrate progress…

No matter how small.

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💜 What habit has Fibromyalgia given you?

Maybe you always look for a chair.

Maybe you carry a bag full of “just in case” items.

Maybe you automatically calculate how much energy everything will take.

I’d love to know what habit this illness has given you.

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07/06/2026

💜 FIBRO & ME 💜

🔥THE FEAR OF NOT KNOWING HOW BAD TOMORROW WILL BE🔥

One of the hardest parts of living with Fibromyalgia isn’t always the pain you feel today…

It’s the fear of what tomorrow might bring.

Healthy people usually expect tomorrow to be much like today.

They make plans.

Accept invitations.

Book holidays.

Arrange appointments.

They trust their body to be there for them.

Fibromyalgia changes that completely.

Because when your body becomes unpredictable…

Tomorrow stops feeling like something to look forward to.

It becomes something to worry about.

And living with that uncertainty every single day is emotionally exhausting. 💜

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💜 GOOD DAYS DON’T ALWAYS FEEL SAFE

A good day should bring relief.

Instead…

Many of us become cautious.

The pain is quieter.

We have more energy.

Our body feels a little kinder.

But instead of relaxing…

We start wondering…

“How long will this last?”

“Will I pay for today tomorrow?”

“Am I doing too much?”

Fibromyalgia teaches us that even good days can disappear without warning.

And that makes it difficult to completely enjoy them.

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💜 MAKING PLANS BECOMES DIFFICULT

Most people happily make plans weeks in advance.

People living with Fibromyalgia often hesitate.

Will I be well enough?

Will I have to cancel?

Will I wake up in a flare?

Will I disappoint everyone again?

Every invitation comes with uncertainty.

Not because we don’t want to go…

But because we genuinely don’t know what our body will allow.

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💜 YOU STOP TRUSTING YOUR OWN BODY

One of the cruellest things Fibromyalgia steals…

Is confidence.

There was a time when you trusted your body.

You expected it to work.

Now…

Pain can appear without warning.

Fatigue can hit within minutes.

Brain fog can suddenly take over.

A simple task can trigger a flare.

When your own body becomes unpredictable…

It becomes difficult to feel completely safe inside it.

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💜 EVERY DECISION HAS A PRICE

Before Fibromyalgia…

You simply lived your life.

Now every decision comes with questions.

If I clean today…

Will I spend tomorrow in bed?

If I go shopping…

Will I manage the walk back?

If I enjoy myself today…

Will my body punish me later?

Living with Fibromyalgia often feels like constantly negotiating with your own body.

And those calculations never really stop.

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💜 THE WORRY NEVER FULLY LEAVES

Even during better moments…

Part of your mind stays alert.

Will the pain come back?

Will I sleep tonight?

Will tomorrow be worse?

Should I rest now?

Should I stop before I overdo it?

That constant uncertainty creates a quiet anxiety that most people never see.

It is exhausting always waiting for your body to change.

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💜 YOU LEARN TO APPRECIATE THE LITTLE THINGS

Living with uncertainty changes your perspective.

A low-pain day feels precious.

A peaceful night’s sleep feels like a gift.

Being able to leave the house becomes something to celebrate.

Feeling mentally clear for a few hours feels amazing.

Fibromyalgia teaches you to treasure moments that many people take for granted.

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💜 LIVING WITH UNCERTAINTY TAKES INCREDIBLE STRENGTH

Every single day…

People living with Fibromyalgia keep going.

Even when they don’t know how tomorrow will feel.

Even when plans might fall apart.

Even when pain changes without warning.

Even when exhaustion refuses to leave.

That isn’t weakness.

That is resilience.

It takes enormous courage to keep moving forward when your own body refuses to give you certainty.

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💜 Take Away 💜

Fibromyalgia doesn’t just create pain.

It creates uncertainty.

It teaches you to question tomorrow.

To be cautious with hope.

To think carefully before making plans.

To wonder what your body will allow.

If you live with that uncertainty every day…

Please remember this.

You are not negative.

You are not unreliable.

You are not weak.

You are adapting to an illness that never gives you guarantees.

And every time you wake up and face another day without knowing what your body has planned…

You are showing a quiet strength that deserves far more recognition than it receives. 💜

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