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Link between traumatic experiences and Endometriosis Link!

Recent research suggests that childhood and adult trauma, including emotional, physical, and sexual abuse, may increase the likelihood of developing endometriosis. At Relevant Partners, we have raised this question over the past 20 years and are pleased to see that scientific evidence is now emerging.

A recent study published in JAMA Psychiatry investigated the connection between traumatic experiences and endometriosis using both observational and genetic data. The researchers explored how trauma history and genetic predisposition might influence the risk of developing endometriosis. They focused on women who had experienced childhood maltreatment or interpersonal trauma and found that these women had higher odds of developing endometriosis compared to those who had not faced such events. Specifically, events related to childhood abuse, abusive partners, and severe emotional distress were linked to increased risk. Additionally, women with endometriosis were more likely to experience stress-related conditions such as anxiety and depression.

Importantly, while both trauma and genetic predisposition independently influenced the risk of endometriosis, the study did not find any direct interaction between the two. This indicates that trauma alone does not directly trigger endometriosis but can be viewed as a contributing factor.

It's also worth noting that the study exhibited cultural bias as it relied primarily on European-centric data and did not include Black and Brown women.

In conclusion, although this research provides promising insights and compelling evidence, further studies are needed to confirm the exact link between trauma and endometriosis, particularly with the inclusion of Black and Brown women in the data collection. From an initial medical consultant's perspective, this emphasises the importance of considering psychological history when screening and diagnosing endometriosis.

Endometriosis and Autoimmune Disease

A recent study conducted by researchers at the University of Oxford has confirmed a genetic link between endometriosis and conditions such as rheumatoid arthritis, celiac disease, and multiple sclerosis. The findings indicate that women with endometriosis have a 30-80% increased risk of developing autoimmune diseases.

The research team from the University of Oxford stated that this newly discovered link could be used to explore new treatment options that may be effective across these conditions. Professor Krina Zondervan, the joint senior author and head of the Nuffield Department of Women’s and Reproductive Health at the university, remarked that the study provided "valuable new insights into disease biology." She emphasised that they have established solid evidence of a connection between endometriosis and a heightened risk for diseases such as osteoarthritis and rheumatoid arthritis, demonstrating that this link has a biological basis.

This new information can be leveraged to identify treatment avenues that may benefit patients with both endometriosis and autoimmune conditions. As a result, women with endometriosis should be closely monitored for the potential development of autoimmune diseases.

The full paper can be read in the Human Reproduction journal, external.

Exciting Breakthrough: New Daily Pill Approved for NHS Use to Treat Endometriosis

A major advancement in the treatment of endometriosis has arrived! The National Institute for Health and Care Excellence (NICE) has approved the use of a groundbreaking combination drug, relugolix, now available on the NHS in England and Wales. This daily pill offers new hope for thousands of women suffering from the often-devastating effects of this chronic condition.

The Harsh Reality of Endometriosis

Endometriosis affects 1 in 10 women, often leading to excruciating pain, fertility issues, and a significant impact on daily life. A recent BBC investigation highlighted just how life-altering this condition can be, with women reporting struggles in their careers, relationships, mental health, and education. Shockingly, many have admitted to experiencing suicidal thoughts due to the severe pain and lack of adequate support.

Urgent Need for Faster Diagnosis & Better Support

Despite affecting so many women, endometriosis continues to be underdiagnosed and undertreated. Some women endure up to 10 years of waiting before receiving a proper diagnosis and care. The long delays have led to growing demands for improved NHS services, faster diagnosis times, and better awareness to ensure women no longer suffer in silence.

Specialist Endometriosis Care Across the UK

To address the complex needs of women with endometriosis, the NHS has a network of 55 accredited endometriosis centers within NHS trusts across England. These centers, accredited by the British Society for Gynaecological Endoscopy (BSGE), provide expert care and advanced treatments for those affected.

Find your nearest BSGE-accredited center here: BSGE Accredited Centres.

A Step Forward – But More Needs to Be Done

While the approval of relugolix marks a significant step forward, campaigners and healthcare professionals stress the need for continued awareness, research, and funding to ensure endometriosis sufferers receive timely and effective treatment.

This new drug offers renewed hope, but it must be accompanied by improved NHS services, faster diagnosis, and greater awareness to truly transform the lives of those battling endometriosis every day.

Stay informed and spread awareness – because no woman should have to suffer in silence.

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Disclaimer: The content of this webpage is intended for informational purposes only. We strongly encourage our readers to use this information only as a preliminary resource. We disclaim any liability for the decisions made by anyone based on this information.