Endometriosis Workplace Support

Dan Poulter Excerpts

Wednesday 9th February 2022 Westminster Hall

[Bell Ribeiro-Addy (Streatham) (Lab)]

It is a pleasure to serve under your chairmanship, Mr Davies. I congratulate the right hon. Member for Elmet and Rothwell (Alec Shelbrooke) on his fantastic opening speech and continued advocacy on this issue. It is so important.

As a member of the APPG on endometriosis and as someone who lives with endometriosis, I am always pleased when it makes it on to the parliamentary agenda. It gives Members an opportunity to discuss the policy changes that need to be introduced. We have heard that the first time it was discussed was 21 years ago, and not enough progress has been made.

During the last debate on endometriosis and polycystic ovary syndrome, I took the time to share my own experience and the difficulties that I and others have daily. I spoke of the general process of going through diagnosis and treatment, because it is not in any way easy. The symptoms go from physical to mental, and it can ruin every single day. Members have been reminded today, and may recall from the last debate, that it takes up to eight years for the average woman to be diagnosed in the UK.

I would like Members to consider what that actually means for people who live with endometriosis every single day. It is eight years, potentially, of living in excruciating pain, waiting for a GP to diagnose the cause of the pain and being gaslighted by the GP and other health professionals while continuously asking about the pain. The pain is so severe that it can prevent someone from carrying out everyday activities, and it can be incredibly disruptive to working.

When I shared my experiences, I did not have the time to talk about how I dealt with my pain at work. When my endometriosis became bad and I was starting to look for a diagnosis, I actually worked here as a parliamentary assistant. Without a diagnosis, people are finding that they have nothing to show their employer to explain why they need time off. When their symptoms are really bad, they have nothing to point to as a legitimate request, in an employer’s eyes, for flexible working.

[Dr Dan Poulter (Central Suffolk and North Ipswich) (Con)]

I thank the hon. Lady for giving way, and I congratulate her on the comments she is making. I also congratulate my right hon. Friend the Member for Elmet and Rothwell (Alec Shelbrooke) for securing today’s debate and for speaking in such a powerful manner.

The hon. Lady speaks from personal experience, and she talks about working in this place and working with an employer who is undoubtedly sympathetic and supportive. To help the Minister address the problems raised in this debate, could she explain what her employer did that made a difference, and what can the Department do to address the problem?

[Bell Ribeiro-Addy]

I thank the hon. Member for his very well-timed intervention; I was just about to get to that. I was very fortunate in that my employer, my right hon. Friend the Member for Hackney North and Stoke Newington (Ms Abbott), did not even wait for me to request flexible working measures. She thrust them upon me.

I had to go to hospital at one point, and when I explained to my right hon. Friend that they were looking towards an endometriosis diagnosis, she began reading up on it. She sent me links almost every day. She understood, and she allowed me to come into work later, because I was having quite bad evenings. She would shout at me if I was doing too much—the only time she would shout at me, just to let Members know. She gave me an entire month off after my botched laparoscopy, after which she threatened to go to the hospital and tell the doctors about themselves. We are not necessarily asking for people to be that extreme in making flexible working arrangements and allowances for their employees, but there are instances where people can be very good.

After becoming a Member of Parliament, I spoke to our accommodation Whip, my right hon. Friend the Member for Alyn and Deeside (Mark Tami). At first, I was told that the way to get a better, more suitable office was to be very nice to him. I spent my time complimenting his ties, and I eventually explained to him what my issue was—not in much detail, but he understood immediately. He did not ask too many questions. He gave me the type of office I needed—one that made it easier for me to get around Parliament. Those are examples of things that employers can do to support women with endometriosis.

We need to urgently bring down waiting times, because going through this can be very difficult. It is not just about waiting times for a diagnosis. It is about follow-up. It is all well and good to diagnose a woman with endometriosis, but if it is not followed up with further treatment after a laparoscopy, it continues. Endometriosis does grow back. Those living with endometriosis need, once they are diagnosed, to be able to understand what they are experiencing and to be able to talk to their employers about their condition, and employers need to take the time to be informed about the condition. But it does not end there. We know that there is no cure for endometriosis, and that treatment at the moment may only be able to ease the pain.

We know just how much endometriosis impacts on people at work. It is worth mentioning again the report of the all-party parliamentary group on endometriosis: 55% of people with the condition having to take time off work is not a small thing, and 27% missing out on promotions because of the condition is not a small thing. Those are issues that women in general already face in the workplace. The report also found that 40% of those with the condition worry that they will lose out in their jobs and further studies, and one in six actually have to give up their work—all because we are not taking care when we need to. We need to support those with endometriosis in the workplace, so that it does not affect their career advancement.

When I was thinking about becoming a Member of Parliament, I had to consider whether I actually could, because I was in so much pain. I had to consider whether I would be able to campaign in the way that we are meant to, and do all the things that we are meant to do. That is not fair for any woman. It is hard enough for women in the House in the first place, and for women in many other workplaces right across the country. For someone to have to think about whether they should continue in a job, or go for a job that they would love, simply because of their condition—simply because that condition does not have the level of importance in policy that it deserves—is not fair at all.

There are several steps that the Government could take. They have to start by clarifying whether endometriosis is covered by the Equality Act 2010. We have to be very clear here. The Equality Act states that a person has a disability if they have a “physical or mental impairment” that

“has a substantial and long-term adverse effect on”

their

“ability to carry out normal day-to-day activities.”

If endometriosis prevents an individual from carrying out their day-to-day tasks—and I promise hon. Members that it absolutely does—they should be entitled to the same protection under the Equality Act that those with diabetes currently have. We know that endometriosis affects as many women as diabetes does. Further clarity on that would go a long way to ensuring that those with endometriosis are not discriminated against in the workplace.

I also join campaigners in calling on this Government to adopt an open culture when discussing menstrual health. For far too long, women have been made to feel ashamed or embarrassed when discussing their bodies. For example, when I was at school we had various names for it—people would say their “cousin had come to stay” or that “the red river was flowing,” and people would pass each other sanitary towels under the table. When it comes to our periods, it is all meant to be shame and embarrassment. Further, the Government have to work with the NHS to ensure that people with endometriosis have the right access and support when it comes to time off work.

I know that I am going on longer that I should, but now is a good time to pay tribute to all of the endo warriors: the many different endometriosis organisations and blogs. There are women like me who would not have coped if they had not had all of that information from other women. It should not have to be like that—we are not always medical professionals—but I would not have been able to physically campaign and put myself forward to stand in this House if I had not read all of those things online, most of which were provided by other women. I am so very grateful to them, but the Government really have to step up to the plate.