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Woman with Severe Endometriosis Urgently Seeks to Freeze Eggs to Preserve Fertility

Iona Hall, 30, from Bristol, urgently seeks to freeze her eggs after major surgery for severe endometriosis reduced her fertility. She has launched a crowdfunder to raise £21,000 for treatment within four months to preserve her chances of starting a family.

·3 min read
Iona Hall The image shows Iona Hall wearing a white t-shirt underneath a denim pinafore, with silver chains layered around her neck. She has long blonde hair and is smiling at the camera, sitting at a desk full of tools used to make jewellery.

Woman with Severe Endometriosis Plans Urgent Egg Freezing

A woman who has undergone major surgery for severe endometriosis is planning to "urgently" freeze her eggs in the hope of starting a family in the future.

Iona Hall, 30, from Bristol, had two operations in 2024 to remove a 10cm cyst on her ovary and to separate her bowels and uterus, which had become fused together.

She has launched a crowdfunder to raise £21,000 needed for three rounds of egg harvesting, which she says must take place within the next four months to preserve her fertility due to a critically low egg reserve.

"It feels frightening, but the little eggs I do have left are good quality, so it's not over."

What is Endometriosis?

According to the NHS, endometriosis occurs when cells similar to those lining the uterus grow in other parts of the body.

It often affects the ovaries, fallopian tubes, and the tissue lining the pelvis.

Symptoms include severe abdominal pain, heavy periods, painful sex, and fatigue.

It is estimated that one in 10 women suffer from the condition, and on average, it takes over eight years from the first GP appointment to receive a diagnosis.

NHS The image shows a diagram of a woman's lower abdomen, with labels identifying the female anatomy. There are yellow clumps visible on the uterus, ovaries and fallopian tubes indicating endometrioma cysts.
The growing tissue causes inflammation, pain, scar tissue, and potential fertility issues

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Hall's Experience with Endometriosis

Hall, a self-employed silversmith, first noticed symptoms after stopping the contraceptive pill, which she said had been "masking" the pain for 10 years.

"When I was in my teens and early twenties I just thought I was getting urinary and kidney infections all the time," she told BBC Radio Bristol.
"I just thought I was one of those unlucky girls. The pain just never went.
It got so bad I was waking up in the middle of the night, throwing up from the pain and writhing around on the floor."

Initially, doctors misdiagnosed Hall at age 24 with chronic urinary tract infections (UTIs) and prescribed her a year's worth of antibiotics.

By the time the correct diagnosis was made, "the endometriosis has spread everywhere," she said.

After two major surgeries, doctors informed Hall that her egg count had dropped to critically low levels.

Her anti-Mullerian Hormone (AMH) levels—a measure of egg reserve—were 11.9 before surgery but have since fallen to 2.1.

For comparison, the average AMH level for a 30-year-old is around 17, Hall said.

Iona Hall The image shows Iona Hall lying in a hospital bed wearing a white gown, looking at the camera.
Hall underwent two major operations to remove cysts that had spread from her lower abdomen up to her diaphragm

"I was really, really upset," she said.
"Freezing my eggs is my only chance to preserve my fertility and give myself the option of a family in the future.
Endometriosis has taken so much from my life, and I don't want it to take this from me too."

Hall's crowdfunder has raised more than £10,000 so far.

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This article was sourced from bbc

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