Lola

Lola developed plaque psoriasis when she was 14. She has only recently noticed that psoriasis can have a big emotional impact on her. Lola would prefer to not rely on medications, like steroid creams, and she has recently started yoga to help with stress.

Lola has had plaque psoriasis since she was 14 years old. Her first patches were on her elbows and scalp. At first, the doctors were unsure if it was psoriasis or a fungal infection. Lola felt disheartened when it was confirmed as psoriasis because she understood that it would be something that stayed with her for life. Her GP gave her a big leaflet about psoriasis but Lola feels there was a lot of information missing, such as that psoriasis is linked with increased risks of arthritis and depression. It was off-putting when Lola discovered about these other health aspects and she says that she doesn’t look online for information as much anymore. Lola’s psoriasis affects different parts of her body; for example, she recently noticed patches of psoriasis in her eyebrows. Having psoriasis on her scalp also caused her lymph glands to swell up once when the skin became infected. Lola’s psoriasis is sometimes also painful and itchy, which has an impact on her sleep. Stress is a major trigger for Lola’s psoriasis and she recently started yoga to help with managing the impact of this on her psoriasis.

Lola has been prescribed different steroid creams and vitamin D creams for her psoriasis. She finds that these are time-consuming to use, especially because she has specific creams for different parts of the body and she has to wash her hands in between using them. Another downside is that putting the creams near her hairline makes her hair greasy. Lola also used a special shampoo for a while but stopped as she didn’t think it helped her scalp psoriasis much. Last year, Lola decided to cut out steroids as she’d heard from a friend that these could have bad impacts on your health. She tried an alternative approach which included Lola changing her diet and trying meditation to cope with stress. Lola says it seemed to work during the summer when she was less stressed and out in sunlight a lot. However, Lola’s psoriasis flared up quite badly due to stress at sixth form and so she has returned to using the steroid creams from her doctor again. During the flare up, she became more self-conscious as the psoriasis spread, including onto her face, and she would dress to cover up her psoriasis. Lola finds that she has to be regular with using the creams or her psoriasis will be more severe. Lola says that another step back with managing her psoriasis is when she wears make-up, as this dries out her skin. She thinks she may be getting a referral for phototherapy (light therapy) soon and she’s hopeful about this.

Lola says that it’s only quite recently that she’s realised how much of an emotional impact psoriasis has on her. Lola hasn’t ever noticed people stare but she says that people ask her about it more when the psoriasis is visible on her face. She thinks that teenagers at school can be judgmental, though she feels less self-conscious about it now that she and her peers are a bit older in sixth form. Lola says that she doesn’t mind explaining about psoriasis so long as the person asking her doesn’t then make the situation awkward or embarrassing. Skin flaking is an especially difficult part of psoriasis for Lola, for example when there are bits of skin on her clothes or desk at school. It can be distracting to see the plaques and Lola has to stop herself from picking at these when trying to concentrate on her studies. Psoriasis has meant that Lola no longer dyes her hair or has it professionally cut, as she’s worried that it would be embarrassing for hairdressers to see the psoriasis on her scalp. She tends now to wear her hair up as she feels it is less itchy and cuts it herself.

Lola says that having psoriasis as a young person can mean extra responsibilities and stress at a time which is already tough with exams and other life decisions. Her advice to other young people with psoriasis is to talk to others with the condition. She also feels that doctors should give more information, such as explaining that there are different types of psoriasis and related health conditions. Lola emphasises that emotional support is important. For example, she appreciates her family, friends, girlfriend and work colleagues who compliment her and make her feel proud when her psoriasis is improving.

The itchiness of her skin keeps Lola awake at night and she sometimes scratch her skin in her sleep.

Age at interview 17

Gender Female

Age at diagnosis 14

Lola finds applying topical treatments time-consuming. She sometimes prioritises areas to focus on, such as her face.

Age at interview 17

Gender Female

Age at diagnosis 14

Lola uses a combination of steroid and vitamin D analogue creams.

Age at interview 17

Gender Female

Age at diagnosis 14

At one time, Lola stopped using steroid creams and tried to manage her psoriasis with a holistic approach.

Age at interview 17

Gender Female

Age at diagnosis 14

Lola’s GP wasn’t sure at first whether her symptoms were psoriasis or a fungal infection.

Age at interview 17

Gender Female

Age at diagnosis 14

Lola thinks she should have been told by her doctors about the chances of developing other conditions, like psoriatic arthritis.

Age at interview 17

Gender Female

Age at diagnosis 14

Lola’s psoriasis is better in the summer, but the effect doesn’t last.

Age at interview 17

Gender Female

Age at diagnosis 14

Having psoriasis on her scalp is difficult for Lola because of the skin flaking.

Age at interview 17

Gender Female

Age at diagnosis 14