**Lancashire Woman’s Struggle with Endometriosis Sparks Calls for Better Diagnosis Options**
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Anna Sherrington, a 48-year-old from Lancashire, has spent years grappling with the debilitating effects of endometriosis, a condition that affects many women yet often goes misdiagnosed. After receiving incorrect diagnoses for years, including irritable bowel syndrome (IBS) and pelvic inflammatory disease, Sherrington was finally identified as having endometriosis at the age of 32.
Reflecting on her experience, Sherrington shared her feelings of frustration and isolation, stating that she felt the need to “crack on with life regardless” of the persistent pain. She described how, like countless other women, she compartmentalised her discomfort and masked her invisible illness for over a decade, only to feel dismissed by healthcare professionals.

Endometriosis is characterized by tissue similar to the lining of the uterus growing outside the uterus, often affecting the ovaries, fallopian tubes, and pelvic lining. According to the Mayo Clinic, this can result in severe pain and complications for those who suffer from it. The condition currently impacts over 11% of women in the United States alone, as reported by the Office on Women’s Health.
Sherrington has undergone multiple surgeries in her quest for relief, including five laparoscopies and a hysterectomy. She advocates for the need to develop less invasive diagnostic methods for endometriosis, expressing her belief that current practices are outdated. “It’s almost barbaric that you have to undergo surgery to receive a diagnosis,” she said, calling for more investment in research to improve options available for patients.
As Sherrington pointed out, “Unless we pour money into research, this situation is not going to change.” Many women face long waiting times for diagnosis, leading to feelings of frustration and, in some cases, medical gaslighting. Her calls for reform are echoed by researchers in Scotland who are currently investigating blood tests as a potential alternative for diagnosing endometriosis.
Dr. Gael Morrow, who leads the study at Robert Gordon University in Aberdeen, acknowledged the strain that long wait times place on the NHS and, ultimately, on patients. “With the pressure the NHS is currently facing, finding a less invasive test that can be performed quickly is a priority to improve patient care and treatment,” Morrow stated.
Dr. Lucy Whitaker, a senior clinical research fellow and honorary consultant gynaecologist, also highlighted the necessity for improved diagnostic methods. Her existing research is funded by the charity Wellbeing of Women and seeks to explore non-surgical options for diagnosing endometriosis. She mentioned the current lack of reliable blood or saliva tests in primary care, which further complicates timely diagnosis.
An official from the NHS admitted that many women’s experiences with endometriosis are inadequate, causing potentially significant delays in receiving care. They expressed a commitment to improve the situation through specialized women’s health clinics across England, aimed at providing quicker access to necessary treatments.
In addition to advocating for better diagnostics and treatment, Sherrington has taken proactive measures to raise awareness and funds for endometriosis research. She is set to participate in the 2025 London Marathon, with the goal of supporting the charity Wellbeing of Women. Sherrington believes that increased awareness and investment in groundbreaking research could significantly improve the lives of millions affected by this challenging condition.
As conversations surrounding women’s health continue to evolve, Sherrington’s ongoing journey exemplifies the urgent need for advancements in the diagnosis and treatment of endometriosis. Through her advocacy work, she hopes to inspire a cultural shift in how society perceives and addresses women’s health issues, aiming for more comprehensive and compassionate healthcare solutions.
