Multiple Sclerosis Awareness NG

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Multiple Sclerosis Awareness NG

Dedicated to promoting in Nigeria. By spreading the word & advising the affected on management.

CLICK ON THE LINK TO DONATE
https://www.blessmi.com/fundraiser/3807-multiple-sclerosis-awareness-in-nigeria-initiative

05/12/2025

Summer days, hot showers, crowded buses, all feel like kryptonite to my body.
☀️ MS + heat = instant fatigue and flare-ups.

But here’s the thing:
Knowing your triggers is power.

Ice packs, cold drinks, and air-conditioning aren’t luxuries,

They’re survival tools.
Share your own heat hacks below!

04/12/2025

Ever been mid-conversation and suddenly your brain goes, ‘Wait… what?’
Cognitive fog is no joke.

I laugh, I pause, I apologize, and then I keep going.

MS makes me slower sometimes,

But it doesn’t take away my voice.

Here’s to embracing the pauses and the brain hiccups.

03/12/2025

Imagine sending a message from your brain to your hand… and it gets lost in the cloud. That’s what MS nerve misfires feel like.

It’s funny in theory, frustrating in reality, and invisible to most people.

But for me, each misfire is a reminder of how my body fights its own battles silently every day.

02/12/2025

Some mornings, my legs are my own. Some afternoons, they feel like they’re made of lead.

Walking to the kitchen can feel like a marathon I didn’t sign up for.

MS doesn’t come with a warning.

Unpredictability is part of the package.

Today, I’m sharing this not for sympathy,
But so people understand the invisible battles happening every step of the way.

01/12/2025

Some days, MS fatigue is not just being tired; it’s like my body forgot how to recharge.

People tell me, ‘You look fine,’

But fine doesn’t tell the story of every nerve screaming for rest.

If you live with MS, you know the struggle.

And if you don’t, try imagining running a marathon every morning before even leaving your bed.

That’s a glimpse of MS fatigue.

Today’s reminder:
Fatigue is real, visible or not, and rest isn’t lazy, it’s survival.”

30/11/2025

This month, we have reflected on accessibility, caregiving, inclusion, advocacy, and gratitude, each thread weaving a tapestry of courage.

If you have learned, shared, or connected through these stories
You are already part of the change.

Here’s to every MS warrior,
Every caregiver
Every ally

Your resilience continues to inspire.

29/11/2025

Gratitude doesn’t erase pain; it gives it purpose. For many living with MS, joy is found in small victories:

A pain-free morning
A supportive friend
Or simply being able to move freely today.

Gratitude becomes a daily act of defiance
Choosing to see light where darkness tries to linger.

28/11/2025

Living with MS can feel isolating until you find your tribe.

Communities like MS awareness groups remind us that courage grows when we share space with those who understand.

Every conversation, every virtual meetup, every shared story reminds us: we’re not alone.

27/11/2025

Every story told breaks a bit of the stigma.
Advocacy doesn’t always mean protests or campaigns

Sometimes, it is sharing your story
Educating your community
Or correcting a misconception.

Your voice can spark understanding
Inspire research, and change policy.

Silence hides the struggle.
Advocacy gives it purpose.

26/11/2025

MS patients often navigate multiple specialists, tests, and appointments, sometimes without emotional or informational support.

Inclusive systems start when healthcare providers listen
Simplify processes
And treat every patient as a partner in their own care.

Healing begins when patients are heard.

25/11/2025

Behind every MS warrior is a caregiver, a spouse, a parent, a child, or a friend who shows up every day with quiet strength.

They share in the fatigue, the doctor visits, the uncertainty, and still hold space for hope.

Today, let’s honor those who love and care in unseen ways.

Their love is the medicine we don’t talk enough about.

24/11/2025

It’s not enough to talk about inclusion; we must design for it.

For people living with MS, accessibility means more than ramps and elevators.

It’s about flexible work policies
Remote options
Ergonomic furniture
And understanding colleagues.

Let’s normalize workplaces where physical or cognitive challenges are not seen as limitations but as opportunities to innovate how we work.

Accessibility is not a favor; it’s a right

Address

Abuja

Website

https://msain.org/, https://www.blessmi.com/fundraiser/3807-multiple-sclerosis-awareness-in-nigeria-initiative

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