A lack of facial recognition leads to loneliness for people living with AMD
An inability to recognise faces is causing loneliness for people living with age-related macular degeneration (AMD), research from The Australian National University (ANU) shows.
AMD is a common eye disorder caused by damage to the macular – the part of the eye responsible for our sharpest vision.
The study, published in PLOS One, also found a lack of facial recognition was reducing quality of life and confidence for people with AMD.
“We found people living with AMD are withdrawing from all sorts of social situations because they can’t see faces,” said lead researcher Dr Jo Lane, from The Research School of Population Health.
“Living with AMD can be very lonely. One woman we spoke to couldn’t recognise her son when she answered the door.
“There is a lot of embarrassment about not being able to recognise your family members, friends or people in the community. People can get offended because they think you are being rude or not being friendly.”
Patricia Watson, 82, was diagnosed with AMD seven years ago and no longer recognises her daughter.
“My daughter sees me every afternoon after work and I can’t see her face,” Mrs Watson said.
“I can’t go shopping alone. People who know me know I can’t see them and come up and say ‘It’s Jane, good to see you’ and that’s hugely helpful. But you can’t help feeling sad that they have to tell you who they are.
“Even my sister came up to me unexpectedly while shopping and she had to say: ‘Hello Pat it’s Judy’. I couldn’t see her face.”
Mrs Watson admits she has given up on socialising and says living with AMD can be lonely.
“You can see by people’s faces if people want to speak with you or not, but when you can’t see their face you just don’t bother engaging.
“My husband told me I’d talk to a cardboard box if I could. I used to talk to people in queues and when I was able to travel by bus, I’d talk to people at bus stops. Now, I don’t.
“I would never engage a person in conversation now because I can’t see them.”
Dr Lane, with input from The Macular Disease Foundation Australia, designed community resources for people living with AMD, family, friends and carers. The resources include common mistakes with face perception and helpful tips to make life better for people with AMD.
“Things like describing who you are before speaking to someone, or letting the person with AMD know who is in a room – even with mild AMD – can make the world of difference,” said Dr Lane.