Living with polycystic ovary syndrome can be difficult and lonely | Letters

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"Call for Improved Support and Understanding for Polycystic Ovary Syndrome Patients"

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The experience of living with polycystic ovary syndrome (PCOS) can be challenging due to the lack of support and the overwhelming amount of misinformation surrounding the condition. A letter from a woman diagnosed with PCOS highlights her journey, beginning with a misdiagnosis in her teens and a later confirmation at age 34, which came only after seeking help for weight gain and fatigue. Despite being warned about potential health risks associated with PCOS, such as difficulties conceiving, she was primarily advised to focus on weight loss. This advice, however, proved to be an uphill battle, and she spent two years trying to find a suitable diet and exercise plan while grappling with feelings of isolation and frustration at the inadequate support she received from healthcare professionals. The emotional toll of managing the condition alone further exacerbated her struggles with PCOS.

As she navigated her pregnancy, the lack of understanding from maternity care providers became apparent. Although she was fortunate to conceive easily, her concerns regarding the increased risks associated with PCOS—such as miscarriage and gestational diabetes—were largely dismissed by her midwife. She expressed anxiety over her health and the health of her baby, particularly feeling unsupported in addressing her fears. The letter calls for the National Health Service (NHS) to enhance its understanding and support for individuals with PCOS, emphasizing the need for comprehensive education and compassionate care. The writer hopes for improvements in the healthcare system, particularly for future generations, such as her potential daughter, to avoid similar experiences of confusion and neglect in managing their health conditions.

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Thank you for publishing the article about polycystic ovary syndrome (PCOS) by Charlie Brinkhurst-Cuff (I was diagnosed with PCOS – and was soon drowning in misinformation, 22 June). It resonated with my experience of diagnosis and frustration at the complete lack of support. I was first tested in my teens and told my blood test was normal. I was retested at 34 when I went to my GP about weight gain and struggling with exhaustion. When I was confirmed to have PCOS I was warned about the health issues, and told the best thing I could do was lose weight, even though this would be very difficult, and to come back when I was struggling to conceive.

Charlie is right: the amount of time and energy I had to put in to try to understand how to be healthy has been a huge drain. Especially sifting through the masses of misinformation. It took me two years and a lot of hard work to understand a diet and exercise plan that worked for me. It’s been difficult and lonely trying to navigate this on my own.

Despite the warnings, I was lucky and got pregnant easily. Unfortunately, my maternity care is being coloured by a lack of understanding of PCOS. I know I am at greater risk of miscarriage, gestational diabetes and pre-eclampsia, but my midwife dismissed my concerns about all but the diabetes. I had an extra test for diabetes early in my pregnancy, thankfully negative and another booked for 28 weeks. But I have been struggling with anxiety, as I am at greater risk with no support or advice. Being dismissed as worrying about nothing did not help.

TheNHSneeds to provide better understanding and support for people with PCOS. I hope it improves quickly. I would hate, if I have a daughter, for her to have the same experience I have had.Name and address supplied

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Source: The Guardian