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"If the U.S. withdraws from the WHO, it would severely weaken global health initiatives, disrupt pandemic preparedness efforts, and diminish U.S. influence over international health policy."

"If the United States is no longer a member of WHO, Americans around the world would be more susceptible to disease, but they could also carry it back to the United States and infect multitudes."

"It means we are going to see a lot more disease outbreaks become regional and global, and we will see more disease outbreaks from other countries coming into the U.S."

"The bottom line is that withdrawing from the WHO makes Americans and the world less safe."

"Public health disasters that don't have to happen will happen, because those capacities aren't there anymore [because of the US withdrawal from the WHO]."

"President Trump's decision to withdraw from the WHO could have life-threatening consequences for people in the humanitarian contexts where we work as well as in the US."

Will the US Withdrawal from the WHO Affect Public Health?

Jean Bennett, Albert Maguire and Katherine High were awarded the Breakthrough Prize in Life Sciences for developing Luxturna, the first FDA-approved gene therapy for inherited retinal disease. The $3 million prize was presented at a ceremony in Los Angeles.

Jean Bennett, Albert Maguire and Katherine High were awarded the Breakthrough Prize in Life Sciences for developing Luxturna, the first FDA-approved gene therapy for inherited retinal disease. The $3 million prize was presented at a ceremony in Los Angeles.

Luxturna treats Leber congenital amaurosis, a genetic disorder caused by mutations in the RPE65 gene that typically leads to total blindness by early adulthood. The therapy delivers a functional copy of the gene into retinal cells using an adeno-associated virus.

Luxturna treats Leber congenital amaurosis, a genetic disorder caused by mutations in the RPE65 gene that typically leads to total blindness by early adulthood. The therapy delivers a functional copy of the gene into retinal cells using an adeno-associated virus.

Bennett and Maguire first demonstrated the therapy in dogs with RPE65 mutations before advancing to human trials. The couple adopted two of the treated dogs, named Venus and Mercury, during the research process.

Bennett and Maguire first demonstrated the therapy in dogs with RPE65 mutations before advancing to human trials. The couple adopted two of the treated dogs, named Venus and Mercury, during the research process.

Luxturna received FDA approval in 2017 and is priced at $850,000, making it among the most expensive gene therapies in the world. The therapy is currently available in the US, Canada, Australia and Switzerland.

Luxturna received FDA approval in 2017 and is priced at $850,000, making it among the most expensive gene therapies in the world. The therapy is currently available in the US, Canada, Australia and Switzerland.

A separate Breakthrough Prize in Life Sciences was awarded to Swee Lay Thein and Stuart Orkin for research that led to Casgevy, the first CRISPR-Cas9 gene-editing therapy, approved for sickle cell disease and beta thalassemia.

A separate Breakthrough Prize in Life Sciences was awarded to Swee Lay Thein and Stuart Orkin for research that led to Casgevy, the first CRISPR-Cas9 gene-editing therapy, approved for sickle cell disease and beta thalassemia.

Thein identified BCL11A as a gene that regulates fetal hemoglobin production in adults, a finding later used by Orkin's team to develop an approach that disables the gene, prompting cells to produce healthy fetal hemoglobin in place of defective adult hemoglobin.

Thein identified BCL11A as a gene that regulates fetal hemoglobin production in adults, a finding later used by Orkin's team to develop an approach that disables the gene, prompting cells to produce healthy fetal hemoglobin in place of defective adult hemoglobin.

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