Morounfoluwa Debs

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

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

Strong minds still need support. Mental health struggles are real, common, and treatable. #neurolight #neurolightgb #braintumor #braintumorawarness #cancersucks

@NeuroLightGB Early awareness is very important

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

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💪🏻

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

@NeuroLightGB Sharppppp

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

@NeuroLightGB Clock itttttt

Medication can mask symptoms. Imaging reveals causes. Myth: Relief means you’re fine. Fact: Symptom relief doesn’t rule out serious brain pathology. Knowledge is light 🧠✨

@madebyofresh You guys need to see thiss🔥🔥

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 youtu.be/tqR43malU1E?si… a repost would be great too! #dearmoro

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

@NeuroLightGB This is amazing🤍

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.

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

Before treatment, comes understanding. Too often in Africa, families rush into treatment without knowing the type, stage, or options available for brain tumors. 🧠 Understanding the diagnosis gives strength. 🎗️ Asking questions builds confidence. 💛 Awareness changes everything

Every ribbon tells a story. 🎗️ A story of courage. A story of hope. A story that needs our voice. #braintumor #neurolight #childhoodbraintumor

Every one of us has a role to play. By raising awareness, supporting families, funding research, and spreading hope, we can change the future for children with brain tumors. Let’s be the light together.♥️ #neurolight #braintumorawareness