More calls for support for women with endometriosis

Woman told to 'live her life' after some endometriosis removed from her

A Manx resident is lending her voice to the calls for more support for women on the Isle of Man with endometriosis. 

Earlier today Manx Radio spoke to the founders of the Manx Endometriosis Support Facebook group who believe early diagnosis will improve fertility outcomes, alleviate pain and improve overall quality of life for people with the condition.

After listening to the interview, Chloë Love felt the need to share her story. 

"It was shocking to realise how many people have the same issue but there's no definitive treatment plan."

She told Manx Radio she's been having symptoms since her periods started at the age of 12 and now at 29, it's only becoming more and more unbearable. 

"The level of pain I'm in is actively interfering with my quality of life. I can't work my normal office job as I should be" - Chloë

The Douglas resident says she'd like to see endometriosis be acknowledged and more compassion for people with the condition. 

In November last year, Chloë underwent a laparoscopy and was informed in January a 'small amount' of endometriosis was removed but it wasn't enough to be diagnosed. 

"I was told to just go live my life"

She'd like to see referrals being made quicker or for women to be able to get a second opinion if needed.

You can listen to the full interview here: 

In a earlier statement, Manx Care said: "The representatives for Manx Care who are best placed to respond to this are currently unavailable.

"However, diagnosis and treatment of endometriosis forms part of the Women’s Health Strategy which is an important, ongoing piece of work for Manx Care and a response will be provided as soon as possible."

You can listen to the full interview with the founders of the Manx Endometriosis Support Group via Manx Radio's Newscast.