The Lewy Body Society share information on Capgras syndrome 

The Lewy Body Society has shone a light on Capgras syndrome, a condition in which someone believes that their loved ones, or others they know, have been replaced with a double or imposter. 

To illustrate how Capgras syndrome affects families, The Lewy Body Society has shared the story of Rob and his partner Jayne. Jayne lived with symptoms for 10 years, eventually being diagnosed with Lewy Body dementia and dying aged 59. 

You can read Rob and Jayne’s story here: https://www.lewybody.org/capgras-syndrome-my-partner-thought-was-an-imposter/ 

Jacqui Cannon, CEO of The Lewy Body Society, says: 

“It can be particularly difficult if it is the person offering support who is being misidentified and not being trusted. Although Capgras syndrome can be very upsetting, it is important to accept this is part of the condition and is not personal or malicious. There are medications that can help some people experiencing Capgras but not all.” 

Find out more about Capgras syndrome here: https://www.lewybody.org/new-leaflet-to-help-manage-delusions-misidentification-and-capgras-syndrome-in-lewy-body-dementia/ 

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