Jo Cameron’s Rare Mutation Leaves Her Virtually Pain-Free
Jo Cameron’s rare FAAH-OUT and FAAH variants leave her feeling virtually no pain and have opened new directions for pain research.

Jo Cameron reached her sixties before doctors understood something extraordinary about her: she experiences virtually no pain, rarely feels anxiety or fear, and often heals unusually quickly.
Surgery revealed the mystery
Cameron, who lives in Scotland, was referred to pain geneticists in 2013 after needing no pain medication following major operations on her hip and hand. Her history included burns and injuries that she noticed through smell or sight rather than pain.
Pain usually protects us by warning that tissue is being damaged. Cameron’s experience shows that living without it is not simply a superpower; injuries can go unnoticed.
2013
Referred to pain geneticists
2019
FAAH-OUT finding reported
2023
Molecular mechanism mapped
1,145
Genes found with altered activity
Source: University College London

DNA structure illustration via Wikimedia Commons.
The FAAH-OUT connection
Researchers at University College London found a rare mutation in a previously overlooked region they named FAAH-OUT, combined with another variant in the nearby FAAH gene.
FAAH is part of the endocannabinoid system and influences pain, mood and memory. The FAAH-OUT mutation turns down FAAH expression, reducing enzyme activity. Follow-up work also found changes in pathways associated with wound healing and mood regulation.
Why one person matters to millions
Cameron’s biology offers scientists a natural experiment. Understanding how her mutations alter pain signaling could reveal targets for new medicines, particularly for people living with chronic pain.
That possibility is still research, not a ready-made treatment. Reproducing one pathway safely in patients is far more complicated than identifying it.
The geek lesson
Cameron spent most of her life assuming her experience was normal. Careful observation by one doctor turned that personal difference into a scientific discovery—showing how unusual individual cases can illuminate basic human biology.
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