Fay Cartwright, a nurse, has been admitted to hospital 29 times due to endometriosis since 2021, and she estimates that from age 21 onwards, the total is closer to 50 admissions. According to STV News, she launched the support group InverEndo Support for women with endometriosis in Inverness and surrounding areas. 'March is endometriosis action month and, given the lack of action I’ve seen locally and nationally, I wanted to do something,' Cartwright said.
' The group aims to have monthly meet-ups for activities like coffee, cinema trips, walks, community saunas, or other events. Cartwright has alleged that medical professionals have told her that her symptoms are 'all in my head' and 'just a bad period,' and that she has been told to have a baby, radical surgery, or try various contraceptives to 'cure' her endometriosis. ' However, she noted that some consultants have an exceptional manner and make her feel heard, but they are in the minority.
March is endometriosis action month and, given the lack of action I’ve seen locally and nationally, I wanted to do something.
Endometriosis affects one in 10 women in the UK, according to Endometriosis UK. The NHS website describes endometriosis as a condition where cells similar to those in the lining of the womb grow in other parts of the body, with symptoms including heavy periods, severe period pain, and pain in the stomach and back. Cartwright calls for endometriosis to be recognized as a legitimate, chronic condition.
'I find endometriosis isolating at times and have really struggled with my mental health, and I don’t want others to feel how I have felt over the years,' Cartwright said. It is unknown how many women are currently part of or expected to join InverEndo Support, and what specific actions have been taken locally or nationally for endometriosis care that Cartwright refers to as lacking.
So, I have launched InverEndo Support – a support group open to all women in Inverness and the surrounding areas with endometriosis or awaiting a diagnosis.