LASG ISSUES TRAFFIC ADVISORY AHEAD OF FANTI CARNIVAL. (PHOTO). #PRESS RELEASE.

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 LASG ISSUES TRAFFIC ADVISORY AHEAD OF FANTI CARNIVAL The Lagos State Government has announced traffic diversions and restrictions ahead of the Lagos Fanti Carnival scheduled to hold on Monday, 6th April, 2026, around Tafawa Balewa Square (TBS), Lagos Island. In a bid to ensure a seamless and hitch-free carnival procession, vehicular movement will be restricted along major adjoining roads linking TBS. Affected Routes are; King George V Road (by Mobil Filling Station), Flag House inbound TBS, Force Road inbound TBS, Onikan Roundabout inbound TBS, and WaterBoy Roundabout by Old Defence House. Additionally, all link roads to Moloney Road, such as Military Road (by Old Defence Building), Ajasa Street, Boyle Street, and Hawley Street, will be closed to traffic during the event. To ease parking challenges, designated car parks have been arranged for public use, these include; the Yoruba Lawn Tennis Club Car Park, Zone 2 Car Park (opposite Island Club along King George V Road), Museum Kit...
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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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