NIGERIAN PILOTS AND CREW RELEASED IN BURKINA FASO, HEAD TO PORTUGAL. (PHOTO).

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 Nigerian Pilots and Crew Released in Burkina Faso, Head to Portugal Nigeria’s Minister of Foreign Affairs, Ambassador Yusuf Tuggar, has announced the release and departure of the pilots and crew of the Nigerian Air Force C-130 Hercules aircraft (NAF 913) that had been detained in Burkina Faso. In a statement issued on Thursday, Ambassador Tuggar confirmed that  following  engagement in Burkina Faso, the pilots and crew of NAF C-130 (913) have been formally cleared to depart and are currently en route to Portugal via Accra. The minister highlighted Nigeria’s commitment to dialogue and regional cooperation, stating that these efforts continue to yield positive outcomes. Ambassador Tuggar paid glowing tribute to President Bola Ahmed Tinubu for his visionary leadership and steady guidance which he said proved decisive in resolving the matter through constructive diplomacy and peaceful engagement.
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GENE THERAPY OFFERS NEW SICKLE CELL CURE IN THE U. S. (PHOTO).

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 Gene Therapy Offers New Sickle Cell Cure in the US


Sebastien Beauzile, a 21-year-old from Laurelton, Long Island, has become the first person in New York State to be cured of sickle cell anemia using the groundbreaking Lyfgenia gene therapy.


Administered at Cohen Children’s Medical Center, this innovative treatment provides hope for many suffering from the painful genetic disorder, Forbes reported on Sunday.


A Lifelong Battle

Sickle cell anemia causes abnormally shaped red blood cells, leading to severe pain and potential organ damage. Beauzile, diagnosed at just four months old, endured frequent hospitalizations due to intense pain crises, which he described as “10 out of 10” in severity.


Gene Therapy Breakthrough

Developed by Bluebird Bio and approved by the FDA in December 2023, Lyfgenia works by extracting a patient’s blood stem cells, genetically modifying them to include functional hemoglobin genes, and reinfusing them into the bloodstream. This cutting-edge approach marks a major step forward in treating sickle cell disease.

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