Growing up with juvenile vulvar lichen sclerosus, the experiences and care needs of adult women with lichen sclerosus since childhood: a qualitative exploration.
Beth MorrelJanneke H J KampherbeekMarianne J Ten Kate-BooijIrene A M van der AvoortColette L M van HeesKiki M G J WignyCurt W BurgerSuzanne G M A PasmansMarjolein LugtenbergPublished in: The British journal of dermatology (2024)
Age-appropriate life-phase adjusted individually tailored care for women diagnosed with VLS in childhood or adolescence is needed. Care and guidance from childhood onward should encompass a standard of care adapted to the individual as needs change over time. This involves taking interpersonal differences into account, including differences in support network and coping strategies. These findings demonstrate the need for improving awareness and knowledge about (J)VLS among HCPs, especially primary care providers, and among the general public.
Keyphrases
- healthcare
- palliative care
- primary care
- quality improvement
- mental health
- depressive symptoms
- affordable care act
- emergency department
- childhood cancer
- type diabetes
- early life
- pregnant women
- polycystic ovary syndrome
- metabolic syndrome
- smoking cessation
- skeletal muscle
- insulin resistance
- social support
- lymph node
- chronic pain