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💉 Sickle Cell Warrior | 💪 Unbreakable
📖 Sharing real truths, raw strength & health hacks
🌱 Living proof that pain births purpose
💢 Sickle Cell Consultant

https://whatsapp.com/channel/0029Vb4yS6J4Y9

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14/06/2026

SICKLE CELL TRUTH: MY MESSAGE TO MY DAUGHTER LIVING WITH SICKLE CELL ❤️💔

My dear daughter,

I wish I could take away every pain crisis.
I wish I could carry every hospital admission for you.
I wish I could fight every battle on your behalf.

But there is one thing I need you to know:

❤️ You are stronger than you think.

There will be days when your body hurts.
There will be days when people don't understand your struggles.
There will be days when you ask, "Why me?"

But please don't let sickle cell tell you who you are.

You are not your pain.
You are not your diagnosis.
You are not your hospital records.

You are a fighter.
You are loved.
You are beautifully made.
You have a purpose that no illness can take away.

One day, I hope you look back and realize that every challenge you faced helped shape the incredible woman you became.

And whenever life gets hard, remember this:

Your father believes in you.
Your family believes in you.
And most importantly, God has not forgotten you.

Keep smiling.
Keep dreaming.
Keep fighting.

Because your story is bigger than sickle cell. ❤️🩸

💬 If you could send one message to your child, your parent, or your younger self living with sickle cell, what would it be?

Let's read your messages below. 👇❤️

Fasan Oluwatosin
Sickle Cell Advocate || BROS ME
Founder A Warrior with Purpose

13/06/2026

❤️ THANK YOU, COMMUNITY!

Recently, I shared a sickle cell caregiver webinar with this community, and the response was incredible.

The organizers reached out to let me know they received significant support following the post.

This is proof that when we come together as warriors, caregivers, advocates, and supporters, we can make a real difference.

Thank you for trusting BROS ME and for always showing up for causes that matter.

🤝 We remain committed to supporting sickle cell awareness, caregiver support, health advocacy, and community outreach initiatives.

Organizations, nonprofits, and advocacy groups interested in collaborating on impactful projects are welcome to send a DM.

Together, we can reach more lives and create lasting impact. ❤️🩸

For those people who haven't registered for the NOB Foundation for sickle cell cargivers.

Click on the link👇

https://luma.com/b39wzj8o



Fasan Oluwatosin
Sickle Cell Advocate || BROS ME
Founder A Warrior with Purpose

12/06/2026

Which one below impacts your life the most?

10/06/2026

📢 ATTENTION ALL SICKLE CELL MOMS & CAREGIVERS ❤️

Being a parent of a sickle cell warrior is not easy.

The sleepless nights.
The hospital visits.
The emotional stress.
The constant worry.

While we often focus on the warriors, we sometimes forget the incredible mothers and caregivers who fight alongside them every day.

That's why I'm sharing this special opportunity from the No One Behind (NOB) Foundation.

💜 WARRIOR MOM EMPOWERMENT WEBINAR

This webinar is designed to support, encourage, and empower mothers and caregivers of children living with sickle cell disease.

If you're a warrior mom, this is for YOU.

📝 Register here:
https://luma.com/b39wzj8o

Tag a sickle cell mom who needs to see this. ❤️👇

Let's continue supporting the people who never stop supporting our warriors.

🤝 Community Partnership Notice

BROS ME is committed to supporting initiatives that improve the lives of sickle cell warriors and their families.

For awareness campaigns, health advocacy projects, community outreach programs, webinars, events, and partnership opportunities, feel free to send a DM.

Together, we can reach more people and make a greater impact. ❤️🩸



Fasan Oluwatosin
Sickle Cell Advocate || BROS ME
Founder A Warrior with Purpose

09/06/2026

🧠❤️ SICKLE CELL TRUTH: YOU CAN'T WALK IN PURPOSE WITH A BROKEN MINDSET

Sickle cell can attack your body.

But if you're not careful, it can also attack your mind.

The pain...
The hospital visits...
The missed opportunities...
The disappointment...
The people who gave up on you...

All of these can make you start believing that your life will never get better.

💔 That's the real danger.

Because the moment you lose hope, you stop fighting for your future.

As warriors, we must care for our minds just as much as we care for our bodies.

Your diagnosis is not your destiny.

You are more than your crisis.
You are more than your scars.
You are more than your medical records.

God still has a purpose for your life.

The journey may be difficult, but don't let sickle cell convince you that your story is over.

❤️ Heal your mindset.
❤️ Protect your peace.
❤️ Believe in your future.

Because you can't walk fully in your purpose while carrying a mindset that tells you to give up.

💬 Be honest:

What's one negative thought you've had to overcome because of sickle cell?

Let's encourage one another below 👇❤️

Fasan Oluwatosin
Sickle Cell Advocate || BROS ME
Founder A Warrior with Purpose 🪖

07/06/2026

SICKLE CELL TRUTH: WHAT DOES IT MEAN TO HAVE SICKLE CELL THALASSEMIA?

Have you ever heard someone say they have Sickle Cell Thalassemia and wondered what that means?

Many people know about SS, but very few understand Sickle Cell Thalassemia.

Sickle Cell Thalassemia happens when a person inherits a sickle cell gene from one parent and a thalassemia gene from the other parent.

The result?

A condition that can cause many of the same struggles faced by sickle cell warriors.

💔 Pain crises
💔 Extreme tiredness and weakness
💔 Frequent hospital visits
💔 Low blood levels (anemia)
💔 Missed school, work, and important life moments

For some warriors, the pain can be mild.

For others, it can be severe and life-changing.

That's why it's important to remember that not every person's journey looks the same.

One warrior may look healthy on the outside while silently battling pain, fatigue, and emotional stress every day.

This is also why genotype testing and awareness matter.

Many families have never heard of thalassemia until it affects someone they love.

The more we talk about it, the more lives we can educate and help.

❤️ If you are living with Sickle Cell Thalassemia, your struggle is real.
❤️ Your pain is valid.
❤️ Your story deserves to be heard.

💬 Let's raise awareness:

Before today, had you ever heard of Sickle Cell Thalassemia?

And if you live with it, what is one thing you wish people understood about your condition?

Share your thoughts below 👇❤️

Fasan Oluwatosin
Sickle Cell Advocate || BROS ME
Founder A Warrior with Purpose 🪖

06/06/2026

SICKLE CELL TRUTH: WHAT
AS + AS REALLY MEANS

Many people have heard the phrase "AS + AS", but not everyone understands what it
means.

Here's a simple explanation:

When both parents have the AS genotype, every pregnancy comes with these possibilities:

🟢 25% chance of AA (No sickle cell trait)
🟡 50% chance of AS (Carrier of the trait)
🔴 25% chance of SS (Sickle Cell Disease)

What many people don't realize is that love alone cannot change genetics.

That's why genotype testing is so important before marriage and family planning.

This isn't about fear. This isn't about
judgment.

It's about awareness, informed decisions, and protecting future generations.

As a sickle cell warrior, I believe knowledge is one of the strongest tools we have in the fight against sickle cell disease.

❤️ Get tested. ❤️ Know your genotype. ❤️ Encourage your loved ones to do the same.

One conversation today could change a family's future tomorrow.

💬 Let's educate each other:

When did you first find out your genotype? Before marriage, during school, or later in
life?

Share your story below 👇❤️



Fasan Oluwatosin
Sickle Cell Advocate || BROS ME
Founder A Warrior with Purpose 🪖

05/06/2026

🩸 SICKLE CELL TRUTH: SOMEONE'S BLOOD COULD SAVE A WARRIOR'S LIFE ❤️

One thing many people don't realize is that blood is more than a donation to a sickle cell warrior.

Sometimes, it's hope.

It's the difference between getting stronger and getting weaker.

It's the difference between spending more days in the hospital and getting another chance to go home.

Many warriors have needed blood transfusions at some point in their journey. Some wouldn't be here today without the kindness of a stranger who chose to donate.

Imagine saving a life without ever meeting the person.

That's the power of blood donation.

To every blood donor reading this:

❤️ Thank you.
❤️ You are a hero to someone.
❤️ Your donation may have given a warrior another birthday, another smile, or another chance at life.

And to my fellow warriors:

Have you ever received a blood transfusion that helped you through a difficult time?

Share your experience below and let's raise awareness together. 👇❤️🩸



Fasan Oluwatosin
Sickle Cell Advocate || BROS ME
Founder A Warrior with Purpose 🪖

04/06/2026

"When I tell people I'm SS, they look at me as if I'm going to die very soon."

Those words from Adekunle Gold hit hard.

For many people living with sickle cell, the pain isn't just physical. It's also the assumptions, the fear, the pity, and being treated like your future has already been decided.

The truth is that sickle cell warriors are more than their diagnosis.

They have dreams.
They have talents.
They have goals.
And they deserve to be seen for who they are—not just the condition they live with.

This video is a reminder that sickle cell does not define a person's worth or limit their purpose.

❤️ If you're a warrior, keep fighting.
❤️ If you know a warrior, keep supporting them.

💬 Have you ever been judged, misunderstood, or underestimated because of sickle cell? Share your experience below.

Let's raise awareness together. 👇



Video credit: ShoBiz TV

02/06/2026

To Every Sickle Cell Warrior Thinking of Giving Up… Please Read This

There is a kind of pain that makes you question everything — your strength, your future, even your reason for still holding on. If you’ve ever felt that way as a sickle cell warrior, this is for you.

To every sickle cell warrior thinking of giving up…

There are days when the pain feels louder than hope. Days when your body feels like it’s fighting against you, and your mind starts asking, “How much more can I take?” If you’ve ever been in that place, you’re not weak for feeling it — you’re human for carrying it.

Living with Sickle Cell Disease is not just about managing crises. It’s about waking up each day and still trying, even when your body doesn’t cooperate, even when no one fully understands what you’re going through.

But here is the truth you need to hear today: your story is not ending in this pain.

You are still here. And being here means there is still more ahead of you than what you are currently facing.

Some days you will not feel strong. Some days you will only survive the day minute by minute. And that is still progress. Surviving is still living.

You are not a burden. You are not forgotten. You are not alone in this fight.

And even on the days when you feel like giving up, please remember this — warriors are not people who never fall. They are people who keep rising, even when it hurts.

Hold on. Not because it is easy, but because your life still has chapters that haven’t been written yet.

If today is all you can manage, then let it be enough.

But don’t stop here.

Keep going.








Fasan Oluwatosin
Sickle Cell Warrior and Advocate || BROS ME
Founder A Warrior with Purpose 🪖

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