this post was submitted on 08 Dec 2023
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236
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] 4 points 11 months ago (1 children)

Great news for folks in Jamaica where I'm from. Pretty common there.

[–] [email protected] 4 points 11 months ago

Now all they need is $2 million.