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IT’S SICKLE CELL AWARENESS MONTH!

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THE KINE 🌕🖤

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1,061,825 görüntüleme • 1 yıl önce •via X (Twitter)

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Beri🌚 profil fotoğrafı
Beri🌚1 yıl önce

Sorry but I had to laugh here.🤣🤣

valking ♔ profil fotoğrafı
valking ♔1 yıl önce

He’s just like me, idk any skit maker or any celebrity, just asherkine 😂

𝐏𝐚𝐝𝐫𝐞 🧸✰ profil fotoğrafı
𝐏𝐚𝐝𝐫𝐞 🧸✰1 yıl önce

I just see your tweet, I first repost and like cause I know it will revolve around love and putting smiles on people face. “Wagwan fam” it’s that moment again to show the people in the society, hidden by the imbalances of fate, love in its pure form. Thanks Man ❤️🐐

Korede🏀💎 profil fotoğrafı
Korede🏀💎1 yıl önce

Haffa Asher Come Shomolu na Abeg That ladylac side

Eleniyan 😎 profil fotoğrafı
Eleniyan 😎1 yıl önce

Thank you broski I’ll love to support in the next one God bless 🙏

The Ilaje Sultan 🫅 profil fotoğrafı
The Ilaje Sultan 🫅1 yıl önce

Very beautiful video to watch. Rest easy Alexis

Iampelumi 🇨🇦 profil fotoğrafı
Iampelumi 🇨🇦1 yıl önce

Extremely painful? I hope he gets through this. I am happy he is survivor

Adémola profil fotoğrafı
Adémola1 yıl önce

thank you asherkine 🩶🩶 your type is rare !! unmarried people should do better picking partners so as not to suffer their kids, it can be avoided love to everyone.

𝕭✞𝖌 𝕺𝖞✞𝖓🤽‍♂️ profil fotoğrafı
𝕭✞𝖌 𝕺𝖞✞𝖓🤽‍♂️1 yıl önce

A day with?

Kingsley #Etiquette Ogbiti profil fotoğrafı
Kingsley #Etiquette Ogbiti1 yıl önce

Thank you so much @asher_kine for raising awareness for #sicklecellawarenessmonth To all people living with #sicklecell you all warriors. God bless you and @Usedivest

Benzer Videolar

It’s still Sickle Cell Awareness Month
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It’s still Sickle Cell Awareness Month

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As Sickle Cell Awareness Month comes to an end, Naomi and Adeola have an important message for you ⬇️
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As Sickle Cell Awareness Month comes to an end, Naomi and Adeola have an important message for you ⬇️

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We funded the Bristol African Caribbean Expo (BACE) to create the ‘Sickle Cell Warriors’ documentary, which aims to raise awareness and understanding of sickle cell. Part one features the voices of people with lived experience of sickle cell. Watch here:
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We funded the Bristol African Caribbean Expo (BACE) to create the ‘Sickle Cell Warriors’ documentary, which aims to raise awareness and understanding of sickle cell. Part one features the voices of people with lived experience of sickle cell. Watch here:

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I’m balling for Sickle Cell Awareness Month. We wanted to use NBA 2K as a platform to spread awareness. Join me with #IBall4SickleCell and visit To learn more please go to NewYork-Presbyterian
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I’m balling for Sickle Cell Awareness Month. We wanted to use NBA 2K as a platform to spread awareness. Join me with #IBall4SickleCell and visit To learn more please go to NewYork-Presbyterian

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It’s Sickle Cell Awareness Month & I’m very emotional to announce ‘It Takes A Village’; my 1 year long campaign to get 16,000 new blood donors from Black heritage backgrounds. To donate through the campaign: #ITAVxSimplySayo #16kdonors #GiveBloodWithSayo
1:16

It’s Sickle Cell Awareness Month & I’m very emotional to announce ‘It Takes A Village’; my 1 year long campaign to get 16,000 new blood donors from Black heritage backgrounds. To donate through the campaign: #ITAVxSimplySayo #16kdonors #GiveBloodWithSayo

Sayo Thee Succulent

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Every year, we post “Happy World Sickle Cell Day” But what exactly are we doing beyond the posts? A child with sickle cell misses school to manage a crisis, but when they return, the system leaves them behind. An adult with sickle cell manages pain daily, but HR only sees missed KPIs. Until we change the way society responds to sickle cell, awareness alone is not enough. Let’s stop typing and start transforming. Happy World Sickle Cell Day!
2:47

Every year, we post “Happy World Sickle Cell Day” But what exactly are we doing beyond the posts? A child with sickle cell misses school to manage a crisis, but when they return, the system leaves them behind. An adult with sickle cell manages pain daily, but HR only sees missed KPIs. Until we change the way society responds to sickle cell, awareness alone is not enough. Let’s stop typing and start transforming. Happy World Sickle Cell Day!

Aproko Doctor Global

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Tobi had Sickle Cell, Tobi has been cured of Sickle cell. Amazing 👏
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Tobi had Sickle Cell, Tobi has been cured of Sickle cell. Amazing 👏

The_Bearded_Dr_Sina

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The cure for sickle cell disorder is now available at sickle cell foundation Nigeria, LUTH. 🥺
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The cure for sickle cell disorder is now available at sickle cell foundation Nigeria, LUTH. 🥺

Hafeezah ❤️

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For #WorldSickleCellDay, we’ve partnered with artist NIKKOLAS SMITH to raise awareness of sickle cell disease, its extreme pain & how blood transfusions can help. ▶️ He created a piece titled “Transfusion” after speaking with multiple sickle cell warriors about their daily struggles.
1:54

For #WorldSickleCellDay, we’ve partnered with artist NIKKOLAS SMITH to raise awareness of sickle cell disease, its extreme pain & how blood transfusions can help. ▶️ He created a piece titled “Transfusion” after speaking with multiple sickle cell warriors about their daily struggles.

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sickle cell bitch
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Sensitive content

sickle cell bitch

tokyo toni media

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Dear Sickle Cell Warrior
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Dear Sickle Cell Warrior

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Sickle Cell Disease now has a cure!!!!!
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Sickle Cell Disease now has a cure!!!!!

Health Simplex

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‘Sickle cell pain feels like glass breaking inside me.' Cianna, Kehinde and Angel all have sickle cell — a blood disorder that mainly affects Black people. It can cause extreme pain known as a 'sickle cell crisis' which can lead to stroke and organ failure. 🎥: NHS Blood Donation 🩸🩹
0:58

‘Sickle cell pain feels like glass breaking inside me.' Cianna, Kehinde and Angel all have sickle cell — a blood disorder that mainly affects Black people. It can cause extreme pain known as a 'sickle cell crisis' which can lead to stroke and organ failure. 🎥: NHS Blood Donation 🩸🩹

NHS England

10,199 görüntüleme • 2 yıl önce

How informed are people on the streets about sickle cell? I teamed up with Nteteɛ Foundation to do a pulse check on what people actually know about sickle cell.
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How informed are people on the streets about sickle cell? I teamed up with Nteteɛ Foundation to do a pulse check on what people actually know about sickle cell.

Ayo of Ibadan

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Sickle Cell: We Are Glad To Have The Bone Marrow Transplant Available In Nigeria We are the first NGO to initiate a collective partnership to establish this bone marrow transplant centre, which is the cure for sickle cell. CEO/National Director, Sickle Cell Foundation Nigeria, Dr Annette Ofunne Akinsete Full Interview:
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Sickle Cell: We Are Glad To Have The Bone Marrow Transplant Available In Nigeria We are the first NGO to initiate a collective partnership to establish this bone marrow transplant centre, which is the cure for sickle cell. CEO/National Director, Sickle Cell Foundation Nigeria, Dr Annette Ofunne Akinsete Full Interview:

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“How An AA + AS Couple Ended Up With a Child Diagnosed With Sickle Cell Beta Thalassemia. The Husband Believed The Baby Had Been Switched At Birth Or That His Wife Had Cheated, So He Requested A DNA Test. This Incident Almost Broke Their Home But What Doctors Later Discovered Completely Changed Everything.” ~ Precious Ekene, Sickle Cell Awareness Expert Reveals…😳
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“How An AA + AS Couple Ended Up With a Child Diagnosed With Sickle Cell Beta Thalassemia. The Husband Believed The Baby Had Been Switched At Birth Or That His Wife Had Cheated, So He Requested A DNA Test. This Incident Almost Broke Their Home But What Doctors Later Discovered Completely Changed Everything.” ~ Precious Ekene, Sickle Cell Awareness Expert Reveals…😳

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📍𝐍𝐚𝐠𝐩𝐮𝐫 Felicitation Program of the Thalassemia and Sickle Cell Warriors.
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📍𝐍𝐚𝐠𝐩𝐮𝐫 Felicitation Program of the Thalassemia and Sickle Cell Warriors.

Nitin Gadkari

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GREAT news for Americans with sickle cell and their loved ones ⬇️
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GREAT news for Americans with sickle cell and their loved ones ⬇️

DrOzCMS

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This is a detailed report on Victoria Gray, a sickle cell patient, who participated in the clinical trial utilizing CRISPR gene editing technology. She now no longer experiences the symptoms of the sickle cell disease.
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This is a detailed report on Victoria Gray, a sickle cell patient, who participated in the clinical trial utilizing CRISPR gene editing technology. She now no longer experiences the symptoms of the sickle cell disease.

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NIH Director Dr. Jay Bhattacharya revealed we have a cure for sickle cell anemia. But it costs $3 million. “Did you know that we have a cure for sickle cell anemia?” “It’s NIH-funded research that did this.” “It costs $3 million for treatment.” “If it cost $3,000, there’d be no more sickle cell anemia.” “It’s a single gene problem.” “We’ve invested in cutting-edge science… but we haven’t invested in the things that actually make those huge advances available to the people of the world.” MAHA Institute
1:02

NIH Director Dr. Jay Bhattacharya revealed we have a cure for sickle cell anemia. But it costs $3 million. “Did you know that we have a cure for sickle cell anemia?” “It’s NIH-funded research that did this.” “It costs $3 million for treatment.” “If it cost $3,000, there’d be no more sickle cell anemia.” “It’s a single gene problem.” “We’ve invested in cutting-edge science… but we haven’t invested in the things that actually make those huge advances available to the people of the world.” MAHA Institute

MAHA Action

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