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Screening can save lives, but it also has harms—false positives and overdiagnosis. This guide breaks myths and gives a simple framework for smart screening decisions.

Screening is one of medicine’s most powerful tools — and one of its most misunderstood. Many people believe screening “prevents” disease. In reality, screening detects disease earlier, which can reduce death and complications for some conditions, in some groups, at specific ages.
A responsible screening culture does two things at once: it encourages early detection where evidence is strong, and it protects people from unnecessary testing where harm can outweigh benefit.
Not true. Screening can produce false positives (abnormal results that are not disease), which can lead to anxiety, repeat testing, biopsies, and sometimes unnecessary treatment. It can also detect slow-growing conditions that might never cause harm (often described as “overdiagnosis”), especially in some cancer screenings.
A normal result reduces probability; it does not eliminate it. Symptoms still matter. If you have persistent red flags (bleeding, unexplained weight loss, a growing lump, progressive breathlessness), a normal screening test should not end the conversation — it should refine it.
Screening is for people without symptoms. Diagnosis is for people with symptoms. Mixing the two causes dangerous delays: symptomatic people should not be “reassured” by a screening-type approach when they need diagnostic evaluation.
Screening should not be a social-media trend or a panic response. It should be structured, risk-based, and linked to follow-up care. A test without a pathway is not prevention — it is uncertainty.
Bottom line: Screening can save lives, but it is not automatically good. The smartest approach is targeted screening plus consistent follow-up and symptom-based care when needed.
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