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

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Health Simplex

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20,337 görüntüleme • 1 yıl önce •via X (Twitter)

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SabiNurse1 yıl önce

This is brillant thumbs up Doctor. God bless everyone behind this development

Esekhalaye Emmanuel 🇳🇬 profil fotoğrafı
Esekhalaye Emmanuel 🇳🇬1 yıl önce

Something a Dr/Prof in medical field in Uniben has found cure and tried out years back if I am not mistaken... Whatever is been discovered in Africa is not easily accepted worldwide until it's from their end;

𝐁𝐚𝐫𝐦𝐛𝐲 𝐏𝐮𝐳𝐨𝐌𝐚𝐟𝐢𝐚𝐬𝐨〽️🔆⚓ profil fotoğrafı
𝐁𝐚𝐫𝐦𝐛𝐲 𝐏𝐮𝐳𝐨𝐌𝐚𝐟𝐢𝐚𝐬𝐨〽️🔆⚓1 yıl önce

Great 👍

So.Gay profil fotoğrafı
So.Gay1 yıl önce

This rising health concern is alarming

4mankind profil fotoğrafı
4mankind1 yıl önce

How many billion $ does it worth

ALUBAY profil fotoğrafı
ALUBAY1 yıl önce

Wow . This is great

keluo profil fotoğrafı
keluo1 yıl önce

@TweetHelperBot get this video

AdeSpyDer HeadMasTer 🇺🇸🦉 profil fotoğrafı
AdeSpyDer HeadMasTer 🇺🇸🦉1 yıl önce

How much is the worth of common sense?

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There’s now a cure for Sickle Cell Disease. But guess how much it costs?
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There’s now a cure for Sickle Cell Disease. But guess how much it costs?

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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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NIH Director Dr. Jay Bhattacharya says the NIH has found a cure for sickle cell anemia. “Some NIH investments have a track record of success.” “For example, just this year, decades-long work of NIH-supported researchers culminated in not just one, but two new gene therapies to cure sickle cell anemia.” “When I was in medical school learning about sickle cell disease, I never expected to see a cure in my lifetime.” “And yet, here we are, thanks to NIH-supported research.”
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NIH Director Dr. Jay Bhattacharya says the NIH has found a cure for sickle cell anemia. “Some NIH investments have a track record of success.” “For example, just this year, decades-long work of NIH-supported researchers culminated in not just one, but two new gene therapies to cure sickle cell anemia.” “When I was in medical school learning about sickle cell disease, I never expected to see a cure in my lifetime.” “And yet, here we are, thanks to NIH-supported research.”

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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.
10:13

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.

Dr. George

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The FDA has approved gene-editing technology that can cure Sickle Cell Disease in patients 12 years or older. At the moment, it’s only available in America and costs $2.2 million per individual.
2:34

The FDA has approved gene-editing technology that can cure Sickle Cell Disease in patients 12 years or older. At the moment, it’s only available in America and costs $2.2 million per individual.

Dr. George

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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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#WATCH | Chandrapur, Maharashtra: On National Sickle Cell Elimination Mission 2047 program, Director of ICMR- CRHCM, Nagpur Dr Manisha Madkaikar says, "The National Sickle Cell Elimination Mission has given the guidelines. One is universal screening. In areas with a very high prevalence of sickle cell disease, the entire population under 40 is screened. Currently, under this mission, it is planned that nearly 7 crore individuals will be screened for sickle cell disease... The other is newborn screening. As soon as a newborn is born, we can test the newborn to determine whether he has sickle cell disease. Newborn screening is important because if you diagnose newborns early, you can give them effective treatment... In antenatal screening, the first visit is an ideal time to screen a pregnant woman. If she is found to be a carrier or affected, we can test her partner. If both are carriers for sickle cell disease, we can counsel them about testing the fetus before 20 weeks' gestational age. If the fetus is affected, the couple can consider options regarding sickle cell disease and the decision about pregnancy termination is left solely to the patients and their family."
1:54

#WATCH | Chandrapur, Maharashtra: On National Sickle Cell Elimination Mission 2047 program, Director of ICMR- CRHCM, Nagpur Dr Manisha Madkaikar says, "The National Sickle Cell Elimination Mission has given the guidelines. One is universal screening. In areas with a very high prevalence of sickle cell disease, the entire population under 40 is screened. Currently, under this mission, it is planned that nearly 7 crore individuals will be screened for sickle cell disease... The other is newborn screening. As soon as a newborn is born, we can test the newborn to determine whether he has sickle cell disease. Newborn screening is important because if you diagnose newborns early, you can give them effective treatment... In antenatal screening, the first visit is an ideal time to screen a pregnant woman. If she is found to be a carrier or affected, we can test her partner. If both are carriers for sickle cell disease, we can counsel them about testing the fetus before 20 weeks' gestational age. If the fetus is affected, the couple can consider options regarding sickle cell disease and the decision about pregnancy termination is left solely to the patients and their family."

ANI

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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:

ARISE NEWS

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We’re delighted to hear that exa-cel has been approved by NICE to treat sickle cell disorder! This innovative gene therapy is the first of its kind, offering a potential cure to people without a stem cell donor.
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We’re delighted to hear that exa-cel has been approved by NICE to treat sickle cell disorder! This innovative gene therapy is the first of its kind, offering a potential cure to people without a stem cell donor.

Anthony Nolan

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Singer BIG FISH opens up about living with sickle cell disease and how he adapted his lifestyle to stay healthy. About 80% of sickle cell patients are in Africa. Nigeria has the largest population of people living with the condition in the world
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Singer BIG FISH opens up about living with sickle cell disease and how he adapted his lifestyle to stay healthy. About 80% of sickle cell patients are in Africa. Nigeria has the largest population of people living with the condition in the world

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WATCH: Dr Diana Atwine, Permanent Secretary at the Ministry of Health, has launched Sikurea Hydroxyurea 500mg capsules, a drug expected to strengthen the fight against sickle cell disease. She says local production of the medicine is aimed at reducing the cost burden on sickle cell patients. #MonitorUpdates 📹: Geofrey Mutumba
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WATCH: Dr Diana Atwine, Permanent Secretary at the Ministry of Health, has launched Sikurea Hydroxyurea 500mg capsules, a drug expected to strengthen the fight against sickle cell disease. She says local production of the medicine is aimed at reducing the cost burden on sickle cell patients. #MonitorUpdates 📹: Geofrey Mutumba

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Sebastien Beauzile is the first person in New York to be cured of sickle cell anemia. For too long, research and treatment for sickle cell disease, which disproportionately affects Black people, have taken a back seat. It's my honor to support Cohen Children’s Medical Center with a $100K donation to invest in their cutting-edge sickle cell treatment and research.
2:10

Sebastien Beauzile is the first person in New York to be cured of sickle cell anemia. For too long, research and treatment for sickle cell disease, which disproportionately affects Black people, have taken a back seat. It's my honor to support Cohen Children’s Medical Center with a $100K donation to invest in their cutting-edge sickle cell treatment and research.

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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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𝐀𝐒𝐊

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"I have lost six jobs because I have sickle cell disease. I’ve also never been in a relationship because of it," says a Kenyan lady named Missy, who is now seeking help!
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sickle cell bitch
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Sensitive content

sickle cell bitch

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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
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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

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So Portable wasn’t lying about Kolu being a sickle cell patient — Eko Savage has confirmed it.
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So Portable wasn’t lying about Kolu being a sickle cell patient — Eko Savage has confirmed it.

𝐀𝐬𝐚𝐤𝐲𝐆𝐑𝐍

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Dear Sickle Cell Warrior
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Dear Sickle Cell Warrior

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