this post was submitted on 08 Dec 2023
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FDA Approves World’s First Crispr Gene-Editing Drug for Sickle-Cell Disease | Landmark decision heralds a new type of medicine that can tackle genetic conditions that are hard to treat (www.wsj.com)
submitted 11 months ago by [email protected] to c/[email protected]
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The key thing about this kind of therapy is that it's not a drug you keep on taking - it's a one-time thing which permanently cures the disease.

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[–] [email protected] 1 points 11 months ago

payed

I think the word you're looking for is "paid". "Payed" is something to do with sailors and ropes or something.

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