Te Whare W膩nanga o Waitaha | 麻豆传媒团队 (UC) doctoral candidate Chelsea Skinner surveyed 603 people with endometriosis and asked them about their experiences living with the chronic, gynaecological condition. Endometriosis is a result of tissue that is similar to the lining of the uterus (endometrium) being found in places outside the uterus.
In New Zealand, endometriosis clinical guidelines were only established in 2020. There had been very little previous research, and limited or delayed access to healthcare remains an issue, Skinner says.
鈥淥ur health system is stretched, and we don鈥檛 have the support that those with endo have in other countries. Endometriosis New 麻豆传媒团队doesn鈥檛 have government funding, and knowledge and understanding of the condition and its prevalence is lacking. We鈥檙e working on current estimates that one in 10 women and those assigned female at birth likely have some form of endometriosis in New Zealand, but it鈥檚 probably higher than this,鈥 she says.
Common endometriosis symptoms include painful periods, chronic pelvic pain, painful intercourse, abnormal bleeding, bowel and bladder problems, fatigue and infertility. There is still uncertainty about what causes the condition, and no cure. Quoting the published article, 鈥渕anagement focuses on symptom relief with varying degrees of success.鈥
The study participants鈥 quality of life was found to be significantly impaired but those with higher levels of self-compassion perceived their symptoms to be less severe, which in turn related to less impairment in quality of life.
Self-compassion is defined as being kind, non-judgmental and understanding towards yourself in difficult times, being in touch with difficult experiences in a mindful and accepting manner and recognising that you鈥檙e not alone in your experience, Skinner says.
鈥淎 lot of people get really frustrated and feel guilty about having to take time off work and study or dealing with other effects of endo. We can鈥檛 really control the symptoms, but we can control how we respond to them.鈥
Skinner鈥檚 advice is to note down the symptoms so people can be specific with their GP. Sometimes it will be necessary to seek a second or third opinion.
鈥淥ften people can get pushed around and not feel validated that their symptoms or experiences are real. You know yourself best, so it鈥檚 important to advocate for yourself,鈥 she says.听
鈥淭here will be days when it is harder to live with this condition, I know this through my own lived experience, but there are people out there willing to support you. Be kind to yourself.鈥
The research, published by Skinner and her supervisor from UC鈥檚 School of Psychology, Speech & Hearing, was published recently in the international journal , coinciding with International Endometriosis Awareness Month.
Sustainable Development Goal (SDG) 3 - Good health and wellbeing
