Multiple Sclerosis Awareness NG

Multiple Sclerosis Awareness NG Dedicated to promoting in Nigeria. By spreading the word & advising the affected on management.

01/01/2026

Dear 2026,I am not asking for a perfect body. Just a kinder year.
One that understands when my legs feel heavy for no visible reason.

One that knows strength doesn’t always look like productivity.

One that allows rest without turning it into failure.

I am stepping into you with Multiple Sclerosis
with a body that sometimes surprises me,

A future that still asks for faith,
and a heart that has learned to be brave in quiet ways.

There is fear here.
Fear of flare-ups. Fear of uncertainty. Fear of plans changing mid-sentence.

But there is faith, too
Faith that I can adapt, adjust, and still find meaning in the in-between.

This year, my goals won’t come with guilt.
I won’t punish myself for slowing down.

I won’t measure progress by how much I endure in silence.

Some days, simply getting through is enough.
I’m choosing grace over unrealistic resolutions.

Listening over forcing.

Healing over hustling.

Presence over pressure.

If I grow, let it be gently.
If I rest, let it be unapologetically.
If I hope, let it be without timelines.

Dear 2026,
Meet me where I am
with courage that doesn’t shout,

A strength that isn’t always visible,
and a heart that keeps choosing to move forward anyway.
That is my quiet promise to you.



As 2025 ends, I am choosing to reflect on the tiny joys that held me together.Not the pain.Not the unpredictability.But ...
31/12/2025

As 2025 ends, I am choosing to reflect on the tiny joys that held me together.
Not the pain.
Not the unpredictability.

But the small moments that made the year survivable:
🌼 Warm sunlight on a calm day
🌼 A message on a difficult morning
🌼 A symptom-light day that felt like a gift
🌼 Laughter that softened the heaviness
🌼 A meal that felt like comfort
🌼 A nap that healed instead of defeated
🌼 Music that reminded me I’m still here
🌼 The quiet victory of making it through another year
MS tries… but joy still finds a way in.
Here’s to closing 2025 with gratitude, not regret.

And stepping into 2026 with softer days and stronger hope.





Showing up with MS is a daily act of quiet bravery. Some mornings, your body feels like it didn’t recharge.Your legs fee...
30/12/2025

Showing up with MS is a daily act of quiet bravery. Some mornings, your body feels like it didn’t recharge.

Your legs feel heavy.
Your thoughts slow down.
Your energy disappears without warning.
But you still show up, in the ways you can.

Courage for us is:
Getting out of bed during a flare
Moving slowly but refusing to stop
Choosing rest when guilt whispers
Asking for help when pride fights back
Holding onto hope even when the body misbehaves
Even on days you can’t show up fully, you’re still trying.

And that is courage, the kind the world doesn’t always notice.





Living with Multiple Sclerosis is more than managing symptoms; it’s managing expenses that pile up quietly, month after ...
29/12/2025

Living with Multiple Sclerosis is more than managing symptoms; it’s managing expenses that pile up quietly, month after month.

People see the courage.
They see the strength.
But they rarely see the cost.

MS comes with hidden financial layers like:

Medications
MRI scans, blood tests & check-ups
Mobility aids and lifestyle adjustments
Transportation on flare days
Special diets, supplements, therapies
Lost work hours because your body decides before you do

This isn’t a pity story
It’s the truth.

MS warriors are fighting physically, emotionally, and financially.
And yet…

We keep showing up.





Dating with MS is a different kind of honesty.I tell someone new:“I may move slower… Some days may be harder… Some plans...
28/12/2025

Dating with MS is a different kind of honesty.

I tell someone new:
“I may move slower…
Some days may be harder…
Some plans may change…
But my heart is steady, loyal, and full.”

MS doesn’t make me less lovable.

It just makes communication deeper, patience sweeter, and love more intentional.

The right person won’t run; they’ll walk with you, at your pace.




People often say, “You’re so strong,” and while it’s meant with love, it can feel heavy.Some days, I don’t want to be st...
27/12/2025

People often say, “You’re so strong,” and while it’s meant with love, it can feel heavy.
Some days, I don’t want to be strong.

I want to be held, understood, or even allowed to fall apart without judgment.

Living with MS requires strength, yes.

But it also requires space to be human, to feel, to cry, and to heal.




Some days, walking feels like moving through thick, heavy sand.My legs know what to do, but the signal gets blurry, slow...
26/12/2025

Some days, walking feels like moving through thick, heavy sand.
My legs know what to do, but the signal gets blurry, slow, delayed, or weak.

It’s not that I’m tired.

It’s that my body is wrestling with itself.

If you ever see me moving slower than usual, please know I’m trying, and winning, one step at a time.




This Christmas, support is more than “Let me know if you need anything.”Support looks like:• Checking in without waiting...
25/12/2025

This Christmas, support is more than “Let me know if you need anything.”
Support looks like:

• Checking in without waiting to be asked
• Understanding when fatigue shows up uninvited
• Offering practical help — meals, rides, or a quiet space
• Choosing compassion over assumptions

For those living with chronic conditions, the holidays can be overwhelming.
Sometimes, the best gift you can give is understanding.



Address

Abuja

Website

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

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