“if you do have a skin condition that is visually apparent where others in the world think it’s an infection and change their behaviour towards you because of that skin condition, and it is on top of that, a condition that is recurring, and on top of that, if you can’t get good medical help to control it, you sort of have the sense that you can’t do anything about it,” said dr. liu. “it’s just going to continue being there forever, even get worse, so it’s very understandable how feelings of a low mood or anxiety can arise from that.”
according to the canadian skin patient alliance, as many as 44 per cent of people living with atopic dermatitis develop depression related to their condition, with 64 per cent also experiencing atopic dermatitis-related anxiety.
atopic dermatitis can also affect sleep because of its physical impact on the skin and psychosocial effects.
self-image and self-esteem can also take a hit when a person deals with eczema because, according to dr. liu, “when we feel we have no control over it and that it’s negatively impacting our image, our relationships with other people in the world, it’s hard to imagine how someone could feel confident and routinely happy and functional in those states.”
the need for awareness and education to stop the stigma
on a grander scale, things such as the media and lack of specialized education amongst healthcare providers also perpetuate the judgement that people with atopic dermatitis face, all of which is driven by a lack of understanding.
because of the lack of understanding, “to the average person, it can look quite scary. this kind of rash that you know is on your face or neck or on your hands where you’re touching people, or you’re a chef, and you’re preparing food, and you wonder and worry,” she said.
“i think it’s a vicious, never-ending cycle where the status quo media misrepresent and misunderstands it,” said dr. liu. “they represent it in a negative light. so, there’s this culture and stigma against atopic dermatitis, which then, in turn, discourages patients from speaking out about it because then, you know, it would be perhaps embarrassing or shameful to publicly admit they have this condition that is being depicted in the media as something scary or strange or bad.”