NHS drugs go-ahead offers lifeline to children with rare muscle-wasting disease
14.05.2026 02:01 | The Guardian World
Medicines watchdog approves two treatments for patients with spinal muscular atrophyHundreds of children with a rare muscle-wasting disease will be able to receive two drugs that can improve their survival in a move parents hailed as a “lifeline”.The National Institute for Health and Care Excellence (Nice) has published final draft guidance recommending that any patient who would benefit can have either drug. Continue reading...
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