Over 95% of UK women with endometriosis face disruptive heavy periods, impacting lives and careers

Over 1.5 million UK women are affected by endometriosis – now a new survey has uncovered the significant toll lesser-known symptoms such as heavy menstrual bleeding (menorrhagia) and fatigue take on their social, emotional, and professional lives.

Nine out of 10 (96%) UK women with endometriosis experience a decline in their quality of life due to debilitating heavy periods and fatigue, yet many never seek medical help, according to a new study from leading iron supplement specialist Active Iron.

A survey of 1,500 women and girls for Endometriosis Awareness Month found that problem periods are often dismissed as merely “part of being a woman”. This is despite many individuals experiencing severe pain, heavy menstrual bleeding and fatigue.

Nearly three-quarters of women diagnosed with endometriosis in the UK reported having heavy periods, leading to menstrual fatigue.

This fatigue affected 74% of surveyed women aged 16 to 55 who have the condition, with 59% describing the fatigue as ‘extreme’. As a result, 84% reported a noticeable difference in their ability to function normally during their period.

Endometriosis is a painful condition where tissue resembling the lining of the womb develops around organs within the abdomen. It is characterised by pain during periods, sexual intercourse, bowel movements and/or urination, as well as chronic pelvic pain. Many women also experience secondary symptoms including heavy bleeding, irregular menstrual cycles, and fatigue.

Despite this, on average, women wait 7.5 years for a diagnosis, and many with heavy menstrual bleeding avoid seeking medical help, thinking it’s normal.

Concerningly, the study revealed that symptoms like heavy periods and fatigue are not limited to women diagnosed with endometriosis.

Notably, 77% of those without endometriosis reported experiencing menstrual fatigue that impacted their daily lives, with 74% lacking the energy or motivation to do everyday tasks as a result.

This leaves many women facing serious physical, social, and emotional challenges due to debilitating symptoms. These issues not only harm their health but also disrupt important parts of their lives, such as work, relationships, and social activities.

More than a quarter of women (27%), irrespective of endometriosis diagnosis, reported being unable to work due to heavy menstrual bleeding and the accompanying fatigue. Approximately one in five (16%) had taken a sick day, while 34% had worked but experienced a decline in their performance.

Home life was similarly impacted, with 23% of all women surveyed saying that problem periods had negatively affected their relationship with their spouse or partner, almost a quarter (24%) avoiding staying overnight at a partner’s house, and 20% struggling to keep up with their children during their menstrual cycle.

As a result of heavy menstrual bleeding and fatigue, 50% of women felt antisocial and didn’t want to spend time with friends or family, leaving 55% feeling isolated and alone when dealing with tiredness from heavy periods. Emotionally, 50% described themselves as feeling unhappy, sad or depressed.

Dr Ria Clarke, registrar in obstetrics and gynaecology, and expert clinician for Active Iron, said: “It’s so important that we can dispel the misconceptions around heavy periods, fatigue and endometriosis, reduce unnecessary delays in diagnosis, and improve the quality of life for millions of women worldwide whose lives are being negatively impacted.

“This is particularly important when you consider that these conditions aren’t exclusive to diagnosed individuals, and 47% of UK women find their current methods for alleviating period-related fatigue ineffective.”

Claire Lynch, head of marketing for Active Iron, added: “With this survey and our campaign, we want to spark meaningful conversations and change the way we talk about endometriosis and heavy periods.

“As we enter Endometriosis Awareness Month, our aim is to shed light on the lesser-known impacts of the condition, like heavy periods and menstrual fatigue, breaking down the stigma around menstrual health and aiding women in better managing their symptoms.”

More than half of women surveyed had been given pain medication to treat endometriosis, while 45% were recommended contraception, and 32% have been prescribed other hormone therapies.

Active Iron’s survey found, however, that women find their current methods to relieve menstrual fatigue ineffective. Many had resorted to consuming more coffee or energy drinks (42%), sleeping more (52%), and doing less activities (48%) to manage tiredness caused by their menstrual cycle.

“Given that menstruation is the leading cause of iron loss worldwide, it’s important to understand the link between heavy periods, low iron levels and fatigue. Rather than covering up tiredness and fatigue with quick fixes, a daily iron supplement can help women address the energy loss associated with diminished iron levels, in turn achieving symptomatic relief and improving their quality of life,” added Dr Clarke.

Many iron supplements are poorly tolerated, leading to debilitating side effects like nausea, constipation and changed bowel habits. This causes women to discontinue them, reducing the chance of improving their iron stores and resulting energy levels.

In contrast, Active Iron is clinically proven to improve iron levels by 94%, whilst avoiding troublesome side effects, resulting in increased energy levels, and longer-term improvements in overall health.

Don’t accept menstrual fatigue, visit activeiron.com/uk to learn more.

£12.4 million to help change choices about work

  • £12.4 million awarded to six innovative new projects to understand barriers to getting into work.
  • Projects include investigating the impact of endometriosis on women’s work choices and how programmes to reduce obesity and type 2 diabetes can improve workforce participation.
  • Funding will help overcome barriers facing those who need the most support getting into work    

Six ground-breaking projects including an investigation looking at how endometriosis impacts women in the workplace have been awarded £12.4 million, the UK Government has announced today (Tuesday 12 September).

The projects comprise the first round of the Labour Market Evaluation and Pilots Fund, and take place over the next two years. The results will help to transform the government’s approach to the jobs market and drive forward research into best practice in employment.

While the UK’s employment rate is higher than a number of other advanced economies, the government is committed to ensure that those who most need help getting into the workplace are supported.

The Chancellor announced a range of interventions to address this at Spring Budget 2023 – including a significant expansion of childcare support, making 30 hours of free childcare a week available to parents from children aged 9 months.

The Labour Market Evaluation and Pilots Fund is part of that and will be used to test new approaches and generate better evidence to help specific groups back into work or to work longer hours.

Financial Secretary to the Treasury, Victoria Atkins, said: “Our jobs record is incredibly strong, with high employment that means millions of people are benefiting from work. But for some, that’s not happening.

“We need to look for solutions that are tailored to help people thrive in the jobs market. This analysis is the first step towards that – looking at specific health conditions or living arrangements to find out what works to help people work.”

Minister for Social Mobility, Youth and Progression Mims Davies MP said: “The vital opportunities and confidence employment gives, helps to transform lives. This is why we are determined to support all those who want to progress to do so, while also driving down inactivity and importantly growing the economy.

“This key new funding for our pilots will enable us to support even more people to move forward in work, including vitally those in supported accommodation and more disadvantaged communities, to help people to break down any barriers to work, so more people can fulfil their employment potential.”

National Statistician, Sir Ian Diamond, said: “The ONS welcomes the opportunity to shine light on this important area with these projects.

“This new analysis will provide crucial insight for decision makers in helping to understand how health conditions impact on people’s working lives and what interventions can help people stay in work.”

One of the projects includes a first-of-its-kind Office for National Statistics (ONS) evaluation which will investigate the impact of endometriosis on women’s participation and progression in the workforce.

Endometriosis can affect around 1 in 10 women, with symptoms including chronic pain and fatigue which can disrupt daily routines, fertility and mental health and time off work may be needed for coping with symptoms.

Previous work has shown that women with the condition often take this into consideration when making career choices, including the likelihood they will need to take significantly more sick leave. This project will improve understanding and help inform government plans to support women with the condition in their careers.

A second project by the ONS will evaluate whether programmes to reduce the risk of developing type two diabetes and obesity improve people’s ability to join the labour market. 

Around 3.8 million people in the UK have type 2 diabetes and 2.4 million are at high risk of developing the disease which can have a strong effect on quality of life, including the ability to workThe evaluation will include reviewing the impact of the Healthier You NHS Diabetes Prevention Programme (DPP), a large scale nine-month, evidence-based lifestyle change programme aimed at people at risk of developing type 2 diabetes.

There will also be a new pilot to address barriers to work faced by those aged 18-24 living in supported housing, which is accommodation provided alongside care, support or supervision to help people live as independently as possible in the community and can act as a pathway to transitioning into work.

To support young people in making that transition, DWP and the West Midlands Combined Authority (WMCA) have developed a Proof of Concept that will test financial support and simplification of the benefits system for 18-24 year olds living in supported housing who move into work or increase their working hours.

This will help them to build their employment prospects further, work towards becoming financially independent and progress into move on accommodation in a planned way. 

Funding will also be allocated to two HMRC projects to evaluate the impact of Tax-Free Childcare on parents’ work choices and women’s return to work after maternity leave. In addition, funding will be provided to DWP to trial employment support and rent incentives to move people out of work or on low earnings into work or onto higher earnings.

Clinical trial for new endometriosis treatment offers hope to millions of women

UK clinical trial for potential new endometriosis treatment, funded by Wellbeing of Women and the Scottish Government, offers hope to millions of women  

  • Researchers have been awarded nearly £250,000 by Wellbeing of Women and the Scottish Government to investigate if a drug called dichloroacetate is an effective treatment for endometriosis 
  • If successful, the drug could be the first ever non-hormonal and non-surgical treatment for endometriosis – and the first new treatment in 40 years  
  • Endometriosis is a debilitating condition that affects around 1.5 million women in the UK, yet it is chronically under-funded and treatment options are limited 
  • Wellbeing of Women and the Scottish Government are working in partnership to improve endometriosis treatment and care – a key aim of Scotland’s Women’s Health Plan.  

A clinical trial to study a potential new treatment for endometriosis is set to go ahead thanks to funding made possible by a partnership between leading women’s health charity Wellbeing of Women and the Scottish Government. 

Researchers from the Universities of Edinburgh, Aberdeen and Birmingham will set up and run the clinical trial, called EPIC2, which will involve 100 women with endometriosis in Edinburgh and London. They will investigate whether a drug called dichloroacetate is an effective pain management treatment for those with the condition.  

Endometriosis affects 1.5 million women and those assigned female at birth in the UK. It occurs when tissue similar to the lining of the womb grows elsewhere in the body, most commonly in the pelvic area. This tissue (known as endometriosis lesions) bleeds during a period but has nowhere to go – and causes inflammation, pain and the formation of scar tissue.  

Earlier research, funded by Wellbeing of Women, discovered that cells from the pelvic wall of women with endometriosis behave differently compared to those without the condition. Researchers from the University of Edinburgh found that these cells produce higher amounts of lactate, a chemical generated by the body to give us energy when there is a lack of oxygen. This creates an environment that supports the development and growth of endometriosis.   

When these endometriosis cells were treated with dichloroacetate, a drug previously used to treat rare metabolic disorders in children, lactate production decreased to normal levels and the size of the endometriosis lesions were reduced.  

The EPIC2 research team will build on this knowledge with their clinical trial to determine the optimum dose of dichloroacetate that will provide the most benefit, both in terms of tackling painful endometriosis symptoms and limiting side-effects. 

 

Dr Lucy Whitaker, Wellbeing of Women researcher and Clinical Lecturer in Obstetrics and Gynaecology at The MRC Centre for Reproductive Health, University of Edinburgh, is leading the research.

She said: “We’re grateful to Wellbeing of Women and the Scottish Government for giving us the opportunity to progress our research and hopefully move another step closer to the reality of a new, non-hormonal and non-invasive endometriosis treatment.  

“We know women with endometriosis desperately want more treatment options and better ways to manage the often-debilitating pain that it causes. Our research so far shows promising results that dichloroacetate can make a huge difference. I hope our new trial will confirm this and give women hope that new treatments and a better quality of life are on the horizon.” 

In the EPIC2 clinical trial, which will start recruiting this autumn, half of the women will receive dichloroacetate while the other half will be given a placebo. These will be allocated at random and taken for 12 weeks. Every woman will complete a series of questionnaires and give blood samples over the course of two-and-a-half-years. 

In a move towards personalised medicine, the dose of dichloroacetate for each woman will be determined by which version of a gene called GSTZ1 they carry. This gene is responsible for the speed at which dichloroacetate is metabolised by the body. Some variants do this more slowly than others, which could lead to a build-up of the drug in the bloodstream and increase the risk of side effects unless the dosage is tailored appropriately. 

Janet Lindsay, Chief Executive of Wellbeing of Women, said: “It is completely unacceptable that there have been no new treatments for endometriosis in 40 years. Too many women and girls are suffering from debilitating symptoms, such as chronic pelvic pain, fatigue and even fertility problems, and current hormonal and surgical treatments aren’t suitable for everyone. 

“Endometriosis is an extremely under-funded area of women’s health, so we are very pleased to partner with the Scottish Government and invest in medical research that could transform how the condition is treated for millions of women.

“Dichloroacetate has the potential to be the very first non-hormonal and non-invasive treatment for endometriosis, which will be truly ground-breaking.

With limited options currently available and no cure, advances like this are long overdue.” 

Maree Todd, Women’s Health Minister for Scotland, said: “Scotland is the first country in the UK to introduce a Women’s Health Plan, with endometriosis being one of its early priorities.

“The Plan includes several actions to help improve care and support for those with endometriosis, including a vital action to invest in further research to develop much needed improvements into treatment and management options for the condition. 

“I am pleased that we are jointly funding research with Wellbeing of Women into what could be the first non-hormonal treatment for endometriosis. It is a stepping stone to ensuring that those with endometriosis are given treatment choices that suit their needs.” 

Dr Ranee Thakar, President of the Royal College of Obstetricians and Gynaecologists, said: “It is really positive news that funding has been secured to research this potential new drug treatment.

“We know current endometriosis treatment options don’t work well for everyone, leaving many women with symptoms that can have a serious impact on their quality of life, affecting their physical and mental health.   

“We look forward to the results of this trial and its potential to improve the day-to-day lives of women and people living with endometriosis.” 

Endometriosis Awareness Month: Gynaecologist reveals her advice for people living with endometriosis

  • One in 10 women have endometriosis, but it takes an average of eight years to get a diagnosis.
  • Gynaecologist from intimate wellbeing brand INTIMINA shares advice for people living with endometriosis and treatment possibilities.
  • Ground-breaking film ‘The Wait’ sees eight-year-old children use their age to symbolise the eight-year delay and the campaign aims to empower and inform people experiencing similar painful symptoms, who also feel unheard or ignored – https://www.youtube.com/watch?v=L6Rz9A6EyG8

March is Endometriosis Awareness Month. Endometriosis is a long-term condition where tissue similar to the lining of the womb grows in other places, such as the ovaries and fallopian tubes, affecting one in ten women worldwide.

Despite the seriousness of the disease, it takes an average of eight years just to get a diagnosis. That’s eight long years of enduring terrible pain and the feeling of not being heard.

To help people experiencing symptoms of endometriosis get the help they need sooner, intimate wellbeing brand INTIMINA UK’s gynaecologist Dr Shree Datta shares her advice and guidance:

How to recognise the symptoms

Endometriosis can present itself in different ways from person to person, so it can be very challenging for doctors to diagnose. Common symptoms which suggest endometriosis include cyclical pelvic pain, pain during intercourse, or pain leading up to and during periods. A change in bowel habit, tiredness, and difficulty conceiving can also be common symptoms, so it is important to seek medical advice early.

Keep a symptom diary

Keeping a pain and symptom diary is the best way to describe all of your symptoms before seeing a doctor. Specifically, note down when you experience symptoms concerning your periods, whether they are getting worse, and how they affect your daily activities.

Possible treatments

It may be worth trying to treat your symptoms initially with simple measures such as heat, gentle exercise, pain relief or hormonal medication, before considering more invasive options such as surgery. For some people, it may not be possible to cure endometriosis, and treatments depend on the type and location of endometriosis and how severe it is. Treatment can include medications such as the contraceptive pill, the Mirena coil and/or surgery. In some cases, a mixture of different treatments is needed.

Diet and exercise

Endometriosis is stimulated by oestrogen, so liver and digestive care through nutrition is important. Eating lots of green vegetables and anti-inflammatory foods, as well as reducing caffeine and alcohol intake can have an impact on the symptoms of endometriosis. Fish oil supplements and Vitamin B12 can help endometriosis-associated pain. Also, exercising regularly can be beneficial.

Advice for people trying to get pregnant

For people who are trying to get pregnant and have endometriosis, we would advise you to consult your gynaecologist early. Start taking pregnancy supplements three months before you want to conceive and have unprotected sex regularly throughout your cycle when trying to conceive. Most people have no problems conceiving, but it’s worth seeking expert help early.

Don’t be afraid to speak up

Endometriosis symptoms vary from person to person. Sometimes it takes a lot of time for people to acknowledge they have a medical condition and seek professional help. It can be uncomfortable speaking to a doctor about intimate health issues for many, but an open and honest relationship is crucial for getting the correct diagnosis. Millions of people have endometriosis, so educating the public and fighting this taboo is the way to help them speak up and get diagnosed sooner.

Dr Shree Datta’s advice follows the release of INTIMINA’s powerful film, named ‘The Wait’, that gives a voice to those suffering from the condition by featuring eight-year-old children whose age symbolises the damning eight-year wait statistic – with each of the youngsters having been alive for as long as it takes to be diagnosed with endometriosis*.

The children speak the actual words of real adult women who spent years of their lives waiting and fighting for an endometriosis diagnosis.

The film can be viewed here: https://www.youtube.com/watch?v=L6Rz9A6EyG8

INTIMINA created ‘The Wait’ film as part of its ongoing Seen + Heard period positivity campaign.

Seen + Heard aims to increase the visibility of menstrual wellbeing across the world, normalise conversations about menstrual health, tackle stigma and bias and raise awareness of conditions like endometriosis – which see millions of people suffering in pain while their voices go unheard.

The Wait follows ‘Period’: a collaboration in 2020 between INTIMINA and Pantone that saw the creation of a shade of red emblematic of a healthy menstrual flow.

Danela Žagar, Spokesperson for INTIMINA, commented: “Endometriosis isn’t a rare disease – it affects one in every 10 women. That’s hundreds of millions of people across the world potentially suffering for years.

“The fact the eight-year statistic hasn’t changed in over a decade is further proof, if it were needed, that we must end the wait for those with endometriosis.

“As a global society we have to be more aware of endometriosis, more sympathetic towards those that have it, to speak up and do everything in our collective power to close the gender health gap and to break the taboos and biases that are not just attached to endometriosis, but to menstrual wellbeing in general.”

Dr Shree Datta added: “Healthcare professionals may assume painful periods are normal if they are unclear on its severity and whether pain relief is required. What’s more, it can be especially difficult examining young teenagers for endometriosis as the findings are not specific and the disease presents differently from person-to-person.

“As such it may take longer to refer people to the correct specialist for further investigation and treatment. It’s heart-breaking to hear that people still suffer in silence when we can support them and provide them treatment to help them through their symptoms – so please come and see us if you have a problem.”

For those looking to find out more about endometriosis or get support, please visit www.endometriosis-uk.org

Eight-year-olds symbolise shocking EIGHT YEAR WAIT for endometriosis diagnosis in menstrual health campaign

Powerful film released by INTIMINA sees children give a voice to people that waited eight years or more for an endometriosis diagnosis

  • One in 10 women have endometriosis, but it takes an average of eight years to get a diagnosis.
  • Groundbreaking new film ‘The Wait’ sees eight-year-old children use their age to symbolise the eight-year delay and to tell the stories of British women who had the disease, yet felt like they were not being heard.
  • The film includes the story of Aisha Belsaria who suffered in pain for 15 years before she was correctly diagnosed.
  • Campaign created by INTIMINA to empower and inform people experiencing similar painful symptoms, who also feel unheard or ignored.

One in 10 women worldwide have endometriosis1, yet despite the seriousness of this disease, it takes an average of eight years just to get a diagnosis2. That’s eight long years of enduring terrible pain and the feeling of not being heard.

Today, to give a voice to those suffering from the condition, intimate wellness brand INTIMINA has released a powerful film that features eight-year-old children whose age symbolises the damning eight-year wait statistic – with each of the youngsters having been alive for as long as it takes to be diagnosed with endometriosis*.

Endometriosis is a long-term condition where tissue similar to the lining of the womb grows in other places, such as the ovaries and fallopian tubes. 

What’s more, with this devastating disease commonly starting in adolescence (and sometimes before) any of the eight-year-olds in the film – and across the world – could develop endometriosis in the near future and face the eight year delay themselves if nothing is done to shorten the time to a diagnosis.

In the film, the children speak the actual words of real adult women who spent years of their lives waiting and fighting for an endometriosis diagnosis. While the average wait for a diagnosis is eight years, several of the women that shared their stories experienced delays of much longer.

In one instance, it took a shocking 30 years for a woman to finally be told she had endometriosis. 

The film can be viewed here: https://www.youtube.com/watch?v=L6Rz9A6EyG8

Selected cases from UK-based women that faced ‘the wait’ and whose accounts are spoken by eight-year-old children in the film:

  • Katie Beales (waited nine years) “Waiting years for a diagnosis made me question my own sanity. At points, I started to believe that it was all in my head. I had so much ambition and this condition took so much away from me. The pain was so bad I couldn’t leave my bed, I would vomit and I couldn’t eat. I became a shell of myself. Endometriosis is lonely. It changed my identity.”
  • Nadine Lewis (waited 12 years): It took me five years to get my stage four diagnosis and a further seven years to be diagnosed with thoracic endometriosis. I often feel trapped inside my body which is constantly under attack. I have had countless A&E admissions, investigations and surgeries and been medically gaslighted. I had three diagnostic laparoscopies with no endometriosis removed. Endometriosis has affected my mental health, fertility, bowel and respiratory health. No one should have to go through this. It should not take this long to be taken seriously.”
  • Aisha Balesaria (waited 15 years): At 15 I had started experiencing dreadful pain during menstruation – pain which grew worse as the years went on. It was tremendously difficult waking up in pain and going to bed in pain and doing the same thing all over again the next day. The pain was so intense, it left me confined to my bed. At some points I felt I couldn’t carry on living with the excruciating pain. The pain I was experiencing was dismissed as ‘bad periods’. I felt completely helpless and hopeless. It was extremely challenging waiting for someone to believe me and over time my symptoms worsened. It would be many years later before I’d receive the correct diagnosis. I felt there was little empathy towards my suffering during the years I tried to get help, and my symptoms were downplayed nearly all of the time.”

INTIMINA created ‘The Wait’ film as part of its ongoing Seen + Heard period positivity campaign. 

Seen + Heard aims to increase the visibility of menstrual wellbeing across the world, normalise conversations about menstrual health, tackle stigma and bias and raise awareness of conditions like endometriosis – which see millions of people suffering in pain while their voices go unheard. 

The Wait follows ‘Period’: a collaboration in 2020 between INTIMINA and Pantone that saw the creation of a shade of red emblematic of a healthy menstrual flow.

Marcella Zanchi, Spokesperson for INTIMINA, commented: “We hope this film, in which the age of the eight-year-olds symbolises the eight-year wait for a diagnosis, can create much-needed conversations about endometriosis and inspire change. Because it is unacceptable that people have to wait eight years just to get help. And it’s important to remember that is only an average: some people wait many more years, even decades of their lives in pain.

Ms Zanchi continued: “Endometriosis isn’t a rare disease – it affects one in every 10 women. That’s hundreds of millions of people across the world potentially suffering for years. The fact the eight-year statistic hasn’t changed in over a decade is further proof, if it were needed, that we must end the wait for those with endometriosis.

“As a global society we have to be more aware of endometriosis, more sympathetic towards those that have it, to speak up and do everything in our collective power to close the gender health gap and to break the taboos and biases that are not just attached to endometriosis, but to menstrual wellbeing in general.”

A UK All Party Parliamentary Group Endometriosis inquiry into the disease surveyed over 10,000 people with endometriosis and found that over half (58%) visited their GP more than 10 times after presenting symptoms, but still no diagnosis was made3.



Further commenting on reasons behind the eight-year wait, INTIMINA UK Expert Gynaecologist Dr Shree Datta said: “Healthcare professionals may assume painful periods are normal, if they are unclear on its severity and whether pain relief is required. 

“What’s more, it can be especially difficult examining young teenagers for endometriosis as the findings are not specific and the disease presents differently from person-to-person.

“As such it may take longer to refer people to the correct specialist for further investigation and treatment. From a patient perspective it can also be uncomfortable taking that first step and speaking to a doctor about issues such as pain during sex – or challenging to describe the symptoms they have.”

Shree continued: “The reasons behind the delay are wide-ranging, but nevertheless every possible action needs to be taken to drive down the wait time for people suffering with endometriosis, and education and awareness is vital to make a commitment to ensure this happens.”

To help people experiencing symptoms of endometriosis get the help they need sooner, Dr Shree Datta shares her advice. More information and resources can be found here: 

https://www.intimina.com/blog/talk-about-endometriosis/

  • It can be difficult to describe all of your symptoms and diagnose endometriosis as the symptoms vary, so keep a pain and symptom diary before you see your GP. Specifically, note down when you experience symptoms in relation to your periods, whether they are getting worse and how they affect your daily activities.
  • A referral to a Gynaecologist may also help explore your symptoms further – by requesting an ultrasound, for example. With this information, discussing the risks and benefits of medication and an operation may help you to decide what’s right to you. 
  • It may be worth trying to treat your symptoms initially with simple measures such as heat, gentle exercise, pain relief or hormonal medication, before considering more invasive options such as surgery.
  • Common symptoms which suggest endometriosis include cyclical pelvic pain, pain on intercourse or pain leading up to and during your periods. You may also experience a change in bowel habits, tiredness and difficulty conceiving, so seek medical advice early. 
  • Think about your diet – there is some evidence which suggests that drinking lots of alcohol and eating lots of red meat can increase some of the symptoms of endometriosis, such as painful periods. Fish oil supplements and Vitamin B12 can help endometriosis associated pain. A healthy balanced lifestyle with regular sleep patterns may also influence your symptoms.
  • If you’re thinking about getting pregnant and you are known to have endometriosis, consult a Gynaecologist early. Start taking pregnancy supplements three months before you wish to conceive and make sure you have sex regularly when trying to conceive. Most people have no problems conceiving, but it’s worth seeking expert help early. 

For those looking to find out more about endometriosis or get support, please visit:

www.endometriosis-uk.org