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World Sickle Cell Awareness Day 2025 - Health - Nairaland

Nairaland ForumNairaland GeneralHealthWorld Sickle Cell Awareness Day 2025 (4062 Views)

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World Sickle Cell Awareness Day 2025 by Dpharmacist(op): 9:11am On Jun 19, 2025
Theme: Global Action, Local Impact: Empowering Communities for Effective Self-Advocacy

Date: June 19, 2025

“Until the pain of sickle cell is felt in the halls of policymaking, the cries of the sufferers will remain in the silence of hospital corridors.”

🇳🇬 Why This Day Matters Deeply in Nigeria

Today, June 19, marks World Sickle Cell Awareness Day 2025, a day globally recognized but painfully personal for millions of Nigerians.

As the country with the highest burden of sickle cell disease (SCD) in the world, Nigeria faces a public health crisis that is both genetic and systemic. An estimated 150,000 Nigerian children are born with SCD every year—yet many die before their fifth birthday due to lack of awareness, poor diagnosis, delayed care, and social stigma.

🧬 What Is Sickle Cell Disease (SCD)?

SCD is an inherited blood disorder that causes red blood cells to become rigid and shaped like sickles, obstructing blood flow and causing severe pain, organ damage, infections, and strokes. While it is not contagious, it is passed genetically—when both parents carry the sickle gene (AS), there's a 25% chance of having a child with SCD (SS).

🧠 The Nigerian Reality: Beyond the Biology

While medical textbooks define SCD in terms of cells and genes, in Nigeria, it’s defined by stigma, silence, and suffering:

Parents often hide their children's condition due to fear of discrimination.

Schools lack support systems for students in constant pain or with frequent absences.

Many marriages still happen without genotype testing, increasing future risk.

Healthcare access is uneven—with rural communities especially underserved.

Patients endure the agony of 'crises' without morphine or expert care due to shortages and poor infrastructure.

📢 2025 Theme: Global Action, Local Impact

This year’s theme reminds us that global conversations must spark local change. In Nigeria, this means:

✅ Making genotype testing compulsory before marriage licenses or university admissions.
✅ Training more health professionals in pain management and crisis care.
✅ Providing free or subsidized hydroxyurea—a life-saving medication still unaffordable to many.
✅ Empowering warrior voices (people living with SCD) to tell their stories, advocate for policy, and break the stigma.

🧒🏽 Children Are Dying Silently. Why?

Despite progress in research and treatment, many Nigerian children with SCD still die young. Why?
Because too many are diagnosed late, treated at home with herbal remedies, or mourned in silence due to lack of access to basic care.

We must move beyond awareness to prevention, protection, and empowerment. Every child deserves to be more than a statistic.

👨‍👩‍👧 What Can You Do?

1. Know your genotype. It's a small test with a life-changing impact.

2. Speak up. Challenge harmful myths and discrimination.

3. Support warriors. Emotionally, financially, socially—every gesture counts.

4. Advocate. Join voices pushing for stronger policies, subsidies, and awareness.

🕊️ In Honour of Our Warriors

To every Nigerian living with sickle cell—your strength is unmatched.
To every parent, sibling, caregiver—you are not alone.
To every child lost too soon—we carry your memory into action.

Let this day be more than a reminder. Let it be a movement. 💪🏾❤️
💬 Join the Conversation

Use hashtags:
#SickleCellAwareness #NigeriaCares #WarriorVoices #June19 #SCD2025 #KnowYourGenotype

Re: World Sickle Cell Awareness Day 2025 by viqSmallz(m): 9:31am On Jun 19, 2025
IVF, PGT and prenatal testing will solve this for those already in a marriage where both couples are of AS or SS genotype and those looking into going in one.

Wish every warrior good health and long life.

#SickleCellAwareness
Re: World Sickle Cell Awareness Day 2025 by MummyWealth14: 9:32am On Jun 19, 2025
Wishing every sickle cell patient good health
Re: World Sickle Cell Awareness Day 2025 by MummyWealth14: 9:33am On Jun 19, 2025
viqSmallz:
IVF. PGT will solve this for those already in a marriage like this and those looking into going in one
Na money be the major constraints for some couple
Re: World Sickle Cell Awareness Day 2025 by advocatebaba(m): 9:35am On Jun 19, 2025
Many still roaming around without any knowledge of Thier genotype. Many still ignorantly tie the wed knot without knowingly the genotype of Thier spouses. See God won't come down to save u if u ignorantly bring that innocent child to come and suffer.
Re: World Sickle Cell Awareness Day 2025 by advocatebaba(m): 9:35am On Jun 19, 2025
Many still roaming around without any knowledge of Thier genotype. Many still ignorantly tie the wed knot without knowingly the genotype of Thier spouses. See God won't come down to save u if u ignorantly bring that innocent child to come and suffer.
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Re: World Sickle Cell Awareness Day 2025 by APCNig: 9:35am On Jun 19, 2025
There are three types of Abiku

1. Sickle Cell patients
2. Ogbanjes who have Spiritual husbands in the other world
3. Ogbanjes who are also Sickle Cell patients.


This is from personal experiences that cannot be shared online
Re: World Sickle Cell Awareness Day 2025 by MufasaLion: 9:37am On Jun 19, 2025
People should stop being selfish and not marry to endanger their offspring. I don't pity any couple that has sickle cell offspring. It was a deliberate thing by them. They deserve the consequences.
Re: World Sickle Cell Awareness Day 2025 by Seunpapa65: 9:38am On Jun 19, 2025
It is well if you are in this era and still marrying blindly for love without doing genotype test e no suppose better for you
Please I will need people opinions on hydroxyurea I have someone who is using it and he no longer have crisis but the major concern is the infertility aspects that comes with it I don't know if it's true or false
Re: World Sickle Cell Awareness Day 2025 by MufasaLion: 9:38am On Jun 19, 2025
APCNig:
There are three types of Abiku

1. Sickle Cell patients
2. Ogbanjes who have Spiritual husbands in the other world
3. Ogbanjes who are also Sickle Cell patients.


This is from personal experiences that cannot be shared online
There's nothing like "ogbanje" in this world. There's nothing like spiritual husband or whatever. You need to outgrow the myth and lies told to you by your ancestors.
Re: World Sickle Cell Awareness Day 2025 by MummyWealth14: 9:39am On Jun 19, 2025
MufasaLion:
People should stop being selfish and not marry to endanger their offspring. I don't pity any couple that has sickle cell offspring. It was a deliberate thing by them. They deserve the consequences.
Have some empathy, some laboratories do offer false test results
Re: World Sickle Cell Awareness Day 2025 by MufasaLion: 9:40am On Jun 19, 2025
Seunpapa65:
It is well if you are in this era and still marrying blindly for love without doing genotype test e no suppose better for you
The most wicked and selfish couples are the ones that knew of their genotype incompatibility and still went ahead to breed sick offspring.
Re: World Sickle Cell Awareness Day 2025 by viqSmallz(m): 9:41am On Jun 19, 2025
MummyWealth14:
Na money be the major constraints for some couple
Yes IVF is expensive. The other option of prenatal testing is cheaper.
Re: World Sickle Cell Awareness Day 2025 by Seunpapa65: 9:42am On Jun 19, 2025
MufasaLion:
The most wicked and selfish couples are the ones that knew of their genotype incompatibility and still went ahead to breed sick offspring.
I dey see am they will talk say my pastor said there's nothing to hard for God to do
Re: World Sickle Cell Awareness Day 2025 by MufasaLion: 9:44am On Jun 19, 2025
MummyWealth14:
Have some empathy, some laboratories do offer false test results
Stop making excuses. At this modern day we all are, an average couple marrying now is aware of reputable places to get a test done. A lot of people are enlightened enough to do the right thing.

Just like the case of one Aunty Esther on X, she was given all the support, monetary and physical but she still ended up with a fake medical result from a mushroom lab. Even till now, she remained adamant to seek a proper care. I don't pity people like that.

I hope her helpers channel the funds to someone else that would appreciate it.
Re: World Sickle Cell Awareness Day 2025 by MufasaLion: 9:46am On Jun 19, 2025
Seunpapa65:
I dey see am they will talk say my pastor said there's nothing to hard for God to do
Pastors in Nigeria are pure businessmen and they thrive easily because the bad state of the country has preconditioned the mind of an average Nigerian to seek hope and comfort in religion.
Re: World Sickle Cell Awareness Day 2025 by Exceed15: 9:46am On Jun 19, 2025
Confirm your genotype before marriage. Love is not enough o
Re: World Sickle Cell Awareness Day 2025 by muyico(m): 9:49am On Jun 19, 2025
Ehyah
Parent mistake day! ................. ............
Re: World Sickle Cell Awareness Day 2025 by OkanlawonB(m):
Nobody need to be ashamed of his or her medical condition. Sickle cell traits is so widely spread that many of us are carriers.
Re: World Sickle Cell Awareness Day 2025 by bobonla: 9:52am On Jun 19, 2025
viqSmallz:
IVF, PGT and prenatal testing will solve this for those already in a marriage where both couples are of AS or SS genotype and those looking into going in one.

Wish every warrior good health and long life.

#SickleCellAwareness
What of couples way both na SS?
Anyway what is the reason behind low view and comments on this forum Seun?
Re: World Sickle Cell Awareness Day 2025 by Pastoshizzy(m): 9:54am On Jun 19, 2025
muyico:
Ehyah
Parent mistake day! ................. ............
Very cruel thing to say.
You could have just shush!
Re: World Sickle Cell Awareness Day 2025 by OkanlawonB(m): 9:56am On Jun 19, 2025
MufasaLion:
People should stop being selfish and not marry to endanger their offspring. I don't pity any couple that has sickle cell offspring. It was a deliberate thing by them. They deserve the consequences.
The awareness level in this regard is still very low.
Re: World Sickle Cell Awareness Day 2025 by MufasaLion: 10:02am On Jun 19, 2025
OkanlawonB:
The awareness level in this regard is still very low.
No, it's not. Stop making excuses for people. Almost everyday, you'll see people posting and asking for advice on whether to proceed with their wedding because both are AS. People know what they're doing.

And to shock you, it's even the educated ones that usually go ahead to do such things. They feel they have money to take care of the kids or they can pray to cure it, etc. People are aware but don't just care. More reason I don't pity many of them.
Re: World Sickle Cell Awareness Day 2025 by truthhurts2: 10:15am On Jun 19, 2025
MummyWealth14:
Have some empathy, some laboratories do offer false test results
That's why it's not advisable to rely just on one testing, do three or four tests from four different Labs/hospitals.


Now to the subject matter: It strikes me to the bone whenever I see an SS individual being forgotten by their parents/family, these peeps go through a lot, the becomes rejected from home, becomes beggers/Nuisance on streets. I have two like that, a lady and a guy. The lady has becomes a intimacy gadget for guys at the street where she's staying because most guys don't know how to give wholeheartedly without being given something in return which is very very bad.
Re: World Sickle Cell Awareness Day 2025 by viqSmallz(m): 10:50am On Jun 19, 2025
bobonla:
What of couples way both na SS?
Anyway what is the reason behind low view and comments on this forum Seun?
Adoption is the way to go for thoes kind of couples.
Re: World Sickle Cell Awareness Day 2025 by Emeka71(m): 11:36am On Jun 19, 2025
viqSmallz:
IVF, PGT and prenatal testing will solve this for those already in a marriage where both couples are of AS or SS genotype and those looking into going in one.

Wish every warrior good health and long life.

#SickleCellAwareness
So, who then are the people celebrating this day?
Re: World Sickle Cell Awareness Day 2025 by muyico(m): 12:10pm On Jun 19, 2025
Pastoshizzy:
Very cruel thing to say.
You could have just shush!
what they can avoid with 1k genotype test,Dan spending millions to save life of d innocent child
Re: World Sickle Cell Awareness Day 2025 by DelilahMakinde(f): 12:44pm On Jun 19, 2025
When is Rhesus blood type day ?

Also very important to know your Rhesus status...
Re: World Sickle Cell Awareness Day 2025 by donslmnstvn(m): 2:00pm On Jun 19, 2025
I am a sickle cell patient too. Unfortunately my parents didn't know what it was then thinking its was an attack from the village.

I lost my immediate younger brother 5years ago due to sickle cell complications & kidney failure.

It's sad that even the educated ones among us in Nigeria are still going into marriage after knowing fully well they are both AS.

God is not a magician that's why he gave us brain to think and make decisive decisions.

Love Is Never enough. I am married now to an AA woman, I have 3kids(A son & 2twins). Marrying my wife then was a difficult task because of the discrimination been painted out as a sickle cell patient.
Re: World Sickle Cell Awareness Day 2025 by Pastoshizzy(m): 2:19pm On Jun 19, 2025
muyico:
what they can avoid with 1k genotype test,Dan spending millions to save life of d innocent child
Yes, you're correct. But life happens (atimes) not the way we expect it. True again..you should take precautionary measures towards such a sensitive issue but how much do you know about this 1k labs and their default AA genotype result (in truth the test vials are meant to be preserved in a certain temperature) but a 1k lab with the generator out of fuel will definitely cause confusion in the least expected ways. Most people in that situation married each other assuming they know their genotype until when they have offsprings.

I'm speaking from experience.
Re: World Sickle Cell Awareness Day 2025 by Pastoshizzy(m): 2:30pm On Jun 19, 2025
MufasaLion:
No, it's not. Stop making excuses for people. Almost everyday, you'll see people posting and asking for advice on whether to proceed with their wedding because both are AS. People know what they're doing.

And to shock you, it's even the educated ones that usually go ahead to do such things. They feel they have money to take care of the kids or they can pray to cure it, etc. People are aware but don't just care. More reason I don't pity many of them.
There other reasons people (even the very educated ones find theirslves in such a situation.
MummyWealth14:
Have some empathy, some laboratories do offer false test results
The woman is not far off point. The vials like I explained are very volatile to heat and without a special freezer that preserves them at a certain temperature the results are altered. If you go just any how lab to do genotype (wey generator no ON) na saara money you pay.
Test results na lotto for Naija, go beta lab and if you don enter am there's bone marrow transplant out there (get the child rid of all that pain).
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