Ellen Vyan, a contestant of traitors, has said that she was laughing by a GP and stated that she had less pain threshold while waiting for 10 years for the diagnosis of endometriosis.

Anglissy’s Ellen said that he was suffering from pain that felt like a “thorny wire around her stomach” before her diagnosis, which she was told that there was “only period pen”.

He said that GPS was required to treat women’s health with more sensitivity and called for better funds from the Welsh government.

Welsh government said that it was Spending £ 3m at a women’s health center in each health board By March 2026.

The Treater Star, originally from Lalnafare-Engnavi in ​​Anglisi- The episode was finished on two – Said that she was diagnosed 10 years after her symptoms started in 2024, just before she appeared in reality shows.

Ellen, now 24, said that when her periods started at the age of 14, she often missed school and sat out of the game, but a GP insisted that she had less pain tolerance.

She said that if she was actually struggling, she was offered a contraceptive pill, but she did not feel comfortable with this option, while sexual active.

She said that she kept suffering so badly that she was unable to walk or leave home.

“Sometimes it happens as if you are repeatedly stabbing,” he said.

“I knew that it was not normal regardless of what I was told.”

Endometriosis is a gynecological condition associated with menstruation where tissue similar to the lining of the womb is found in other areas of the body, including fallopian tubes, pelvis, intestines, vagina and intestines.

In rare cases it has also been found in the lungs, eyes, spine and brain. It was once thought that the only place in the body where the endometriosis did not occur was a spleen, but it was also found in 2020.

Symptoms include pelvic region, fatigue and often weak pain in heavy periods, and the condition is also associated with infertility.

Charity endometriosis research by the UK found that the average diagnosis for endometriosis in Wales was the time Nine years and 11 months in 2024,

It was the longest diagnosis time across the UK and had increased by nine years in 2020.

Ellen said that he was not supported by his GP, while he waited for his diagnosis, saying: “I have been offered a coil or bullet, (but) I was not given anything that was given to me Is so disappointing. “

He said that through his own research, he had made changes in his lifestyle to manage his condition, in which his alcohol and caffeine intake, as well as attaching to low-effects exercise and priority to sleep Dena was involved.

“I am not almost suffering as I used to do … (but) I have done it on my own,” he said.

He said: “I think a story needs to be erased here. Because it is a condition associated with female hormones, people combine symptoms with dramatic and it is really disappointing for me.

“There is a lot of stigma around it and I think the stigma needs to be removed.”

Ellen has called upon the Welsh government to offer more money, better information and more sensitivity for the health of women.

“I think GPS needs to spend more time to discover symptoms and offer other solutions instead of just pill or coil, it is ridiculous,” he said.

The Welsh Sarkar said that endometriosis was one of the eight priorities mentioned in its women’s health plan for Wales.

“We have already funded endometriosis nurses in each health board, developed endometriosis Cymru website and provided £ 50 million additional funds to help cut in the longest waiting time, including female The pathological conditions are involved, “said this.

The added £ 3m will be used to establish a women’s health center in every health board by March 2026, “to support timely diagnosis and management of menstrual conditions including endometriosis”.