'Adenomyosis may be invisible, its impact is not'
Title: The Hidden Burden of Adenomyosis: A Condition That Affects One in Ten Women
Adenomyosis is a uterine disorder affecting at least 10% of women, characterized by heavy, irregular, and painful menstruation. For some sufferers, the agony is excruciating; one woman described the sensation as having a "chainsaw" operating inside her. Mathilde Barker, a 22-year-old content creator from Surrey who manages over 500,000 followers across TikTok and Instagram, also lives with endometriosis. She recalled her most severe episodes: "When I was at my worst, it genuinely felt like I had a mass in my uterus and that it was dragging behind me."
Medically, adenomyosis occurs when the tissue that normally lines the uterus grows into the muscular wall of the womb. While it shares many symptoms with endometriosis, the conditions are distinct. In endometriosis, similar tissue grows outside the uterus and can spread to other parts of the body, whereas in adenomyosis, the growth is confined within the womb.
The delay in diagnosis and lack of understanding has left many women feeling unheard. A spokesperson for the Department for Health and Social Care expressed deep concern to the BBC, stating, "It is deeply concerning that so many women feel dismissed when they come forward with pain."
For Barker, who was diagnosed with endometriosis at age 19 after laparoscopic surgery and adenomyosis two years later, social media became a vital support network. She noted that her audience quickly connected with her posts, many of whom were experiencing similar symptoms. However, the daily reality of the condition remains challenging for many.
Lauren Buckland, 36, experiences unpredictable "stabbing" pains in her uterus, lower back, hips, and pelvis. She recounted a harrowing experience walking home from work, overwhelmed by pain and tears, unsure of the cause. "This is my body and it's not working how I'd like it to work, but I've got to work with it," Buckland said. "It's a bit frustrating, but it's just being a woman, isn't it?"
Emma Blackburn, a 34-year-old from Broadstairs in Kent, endures constant pain, which she compares to labor. "All of a sudden it'll be what I can only describe as sort of like a labour pain... it'll just shoot into my pelvis," she explained. Blackburn, who also suffers from fibromyalgia and endometriosis, structures her life around her menstrual cycle. During each period, she passes clots ranging in size from a 5p to a 50p coin.
Blackburn advocates for greater public education regarding women’s health, emphasizing the profound impact these conditions have on both physical and mental well-being. Lesley Salem, founder of the workplace training organization Over the Bloody Moon, agrees. "We want to make sure that hormonal health and menstrual health isn't a barrier," Salem said, noting that education is key to driving change.
Salem highlighted that a lack of awareness persists, and a significant stigma remains in professional environments. This often causes women, particularly those early in their careers, to fear disclosing their health struggles. Experts unanimously agree that increased research and education are essential.
Dr. Rebecca Mallick, a consultant gynecologist at University Hospitals Sussex, stressed, "It all starts with education on all levels." She argued that menstruation should be discussed from a young age to establish the common knowledge that periods which disrupt daily functioning are not normal.
Historically, adenomyosis has been difficult to diagnose because a hysterectomy was previously the only method to properly examine the uterus, and the condition is not always visible on scans. However, research is underway to improve detection methods. Dr. Marianne Watters, a clinical researcher with Wellbeing of Women, is investigating whether blood samples can identify the condition. She envisions a future where women might use at-home testing kits for self-diagnosis. "I hope that in the future we'll be able to improve on the ways that we currently diagnose," Watters said. "It is really surprising that we don't know more about this condition and that it's not more openly talked about in the public."
For patients like Zara Dedman, 38, from Kent, the struggle for validation has taken a severe toll. She revealed that being "fobbed off" by doctors has significantly impacted her mental health, noting, "Each day, every month, I am hav"
Source: BBC News Generated at: 2026-05-20 05:10:39 UTC






