Morounfoluwa Debs

Abba's Heritage
Lover of Music
Actress
Link to my latest film

[NeuroLight @NeuroLightGB]

Let’s break some cultural misconceptions
“Not every neurological symptom is spiritual or stress.”

#neurolight #fyp #brainhealth #misconceptions #braintumorawareness

[Morounfoluwa Debs @Foludeb]

One of the most powerful moments was hearing a brain tumor survivor share her story, a reminder that strength, hope, and resilience are real, and that conversations around brain health truly matter. 🧠🤍

This is only the beginning. 🌱

[Morounfoluwa Debs @Foludeb]

What started as a vision became a room full of leadership, purpose, innovation, and impact. ✨

[Morounfoluwa Debs @Foludeb]

Birthing The Leader In You was more than an event, it was a movement focused on empowering young people intellectually, spiritually, and socially while also creating awareness about brain health.

[NeuroLight @NeuroLightGB]

Most headaches are harmless, but when a headache becomes frequent, worse over time and come with vomiting or vision changes, you need to seek medical help🧠✨

#neurolight #braintumorawarness #fyp #ᴄᴀɴᴄᴇʀsᴜᴄᴋs

[NeuroLight @NeuroLightGB]

It’s brain tumor awareness week and throughout this week

A brain tumor is when abnormal cells grow in the brain. Some are cancerous and some are not, but both can affect how the brain works.

We cannot get tired of raising awareness✨🤍

#neurolight #braintumor

[NeuroLight @NeuroLightGB]

Strong minds still need support.
Mental health struggles are real, common, and treatable.

#neurolight #neurolightgb #braintumor #braintumorawarness #cancersucks

[Morounfoluwa Debs @Foludeb]

@NeuroLightGB Early awareness is very important

[NeuroLight @NeuroLightGB]

What’s one thing you think everyone should know about cancer?

[Lady B - IYALODE OF X @mobola_ade]

My name is Zainab. I’m 27 years old. An SS.

That is, I live with sickle cell disease.
My parents are both AS.

Oh, they They knew.
They were told.
They still married.

They said God approved it. They said love would be enough. They said faith would cover the consequences.

I am the consequence.

I was diagnosed before I was two. My childhood memories are not playgrounds or cartoons,they are; hospitals, needles, and adults whispering when they thought I couldn’t hear.

In primary school, I missed classes so often that teachers stopped asking why. Some classmates thought I was pretending. Some thought I was cursed. I learned early how to smile while feeling different.

By secondary school, the pain episodes became more frequent. I would wake up excited for school and end the day on a hospital bed. I watched my mates grow normally while my life moved in pauses, school, hospital, recovery, repeat.

At 15, I lost my younger brother to sickle cell.
We were both SS.

That day changed me forever.

My parents broke down in front of me — crying, apologizing, saying “We followed faith. We didn’t think…”
But the damage had already been done.

Sometimes I forgive them.
Sometimes I resent them deeply.
Both feelings live in me.

In university, I tried to be normal. I joined sickle cell advocacy groups, volunteered with awareness organizations, spoke at events, encouraged parents to test their genotype. People call me strong. They call me a warrior.

What they don’t see is me crying alone at night after another silent pain episode.
They don’t see the fear that comes with planning a future in a body that doesn’t always cooperate.

And Relationships?
That’s another wound.

I’ve been loved… briefly.
The moment conversations turn serious about marriage, children, commitment….they leave. Some are honest. Some ghost me. Some promise forever and disappear quietly.

One man once said he would do anything for me. He talked about taking me abroad, better care, a life without fear. I believed him. For the first time, my heart rested.

Then one day, he stopped calling.

That heartbreak triggered one of the worst crises I’ve had as an adult. Not because of physical stress but because hope collapsed.

Now I’m older. The pain episodes come differently. Less dramatic, but more exhausting. My body recovers slower. My fears are heavier. I ask myself questions my parents never asked each other.

I am strong, yes.
But I am tired.

If you are AS and the person you love is AS, please love your unborn children enough to stop and think. Faith is not a license to ignore knowledge. I am a proof to that

I didn’t ask to be a lesson.
But if my life can prevent another child from being born into avoidable pain, then my voice matters.

That’s why I’m writing this to you. Because people listens to you and this story needs to be heard. I hope that your audience share this till it reaches those who are about to walk by faith and not by sight, Sickle Cell is real!.

Adeyinka, keep rescuing lives, I love how you raise awareness and say the truth unapologetically, those who do not like you are probably those who wish they could be you. Have you met you?. Oh,I see you Queen Ade💪🏻

[NeuroLight @NeuroLightGB]

Early diagnosis isn’t only about cure
It’s about comfort, planning, and quality of life.
Awareness makes a difference. 🧠✨

#neurolight #neurolightgb #braintumorawareness #braintumor #cancersucks #advocacy #fyp #ᴄᴀɴᴄᴇʀsᴜᴄᴋs #neurolight

[Morounfoluwa Debs @Foludeb]

@NeuroLightGB Sharppppp

[NeuroLight @NeuroLightGB]

Clearer images. Better understanding.
MRI uses magnetic fields, not radiation.
Knowledge is light 🧠✨

[Morounfoluwa Debs @Foludeb]

@NeuroLightGB Clock itttttt

[Morounfoluwa Debs @Foludeb]

@madebyofresh You guys need to see thiss🔥🔥

[Oladipo O'Fresh @madebyofresh]

You may have come across this thumbnail on YouTube lately but you didn’t click cos you were not sure it’s worth your time. I want you to know that; that RT is treasure you’ve been ignoring… now go check it out https://t.co/N2v1w81AYN a repost would be great too! #dearmoro

[NeuroLight @NeuroLightGB]

We are young.
We are driven by purpose.
And we believe light can change lives.

Today, we reveal our faces and officially introduce Neurolight — a brain tumor advocacy initiative committed to hope, awareness, and impact across Africa.

Welcome to Neurolight 🤍✨
#neurolight

[Morounfoluwa Debs @Foludeb]

@NeuroLightGB This is amazing🤍

[NeuroLight @NeuroLightGB]

In Africa, a brain tumor diagnosis is more than a medical result,it becomes a full-time battle for access, clarity, and hope.
From long travel distances to cost barriers and emotional stress, patients carry more than symptoms.

[NeuroLight @NeuroLightGB]

Let’s create a culture of informed care, not just fast decisions.