What urgent steps is Iona Hall taking to preserve her fertility?

Iona Hall is urgently seeking to freeze her eggs, requiring £21,000 for three rounds of harvesting within the next four months due to a critically low egg reserve following endometriosis surgery.

What is endometriosis and how does it affect women?

Endometriosis occurs when cells similar to the uterine lining grow elsewhere in the body, often affecting the ovaries and pelvis, causing symptoms like severe abdominal pain and heavy periods. It is thought to affect one in 10 women.

Why does Iona Hall need to freeze her eggs urgently?

Following two major surgeries in 2024 for severe endometriosis, Iona Hall's egg count has dropped to critically low numbers, making egg freezing her only chance to preserve fertility for a potential future family.

Home / Health / Endometriosis survivor's urgent bid for fertility

Endometriosis survivor's urgent bid for fertility

15 Mar

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Summary

Woman, 30, undergoes major surgery for severe endometriosis.
Her egg reserve is critically low, prompting urgent fertility preservation.
She needs £21,000 for three rounds of egg harvesting within four months.

Endometriosis survivor's urgent bid for fertility

Iona Hall, a 30-year-old from Bristol, is urgently pursuing egg preservation due to severe endometriosis. In 2024, she underwent two significant operations to address a 10cm ovarian cyst and the fusion of her bowels and uterus. These procedures have critically depleted her egg reserve, prompting a race against time to freeze her remaining viable eggs.

Hall has launched a fundraiser to gather the £21,000 needed for three rounds of egg harvesting, which must be completed within the next four months. She describes her egg reserve as "critically low" but remains hopeful that the remaining eggs are of good quality, offering a chance at future motherhood. Endometriosis, a condition affecting an estimated one in 10 women, involves uterine-like cells growing outside the uterus, causing severe pain and other symptoms. Diagnosis often takes over eight years. Hall's own journey involved years of misdiagnoses before her condition was identified.

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