Endometriosis Workplace Support

Marion Fellows Excerpts
Wednesday 9th February 2022

(2 years, 2 months ago)

Westminster Hall
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Marion Fellows Portrait Marion Fellows (Motherwell and Wishaw) (SNP)
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It is a pleasure to serve under your chairmanship, Mr Davies. We always thank hon. Members for bringing debates to the Floor—it is a format we use all the time—but I really want to thank the right hon. Member for Elmet and Rothwell (Alec Shelbrooke) for bringing this debate and for his knowledgeable, emotional and compelling speech on endometriosis. I want to say that I am even happier because he is a man: it is still true that the fact that a man brought this important debate makes it even more powerful and will probably get it noticed even more. For that, I think we are all grateful.

It has been referred to already, but the 2020 inquiry by the APPG on endometriosis found that those in work had terrible experiences. I will not go over them, because all the hon. Members who have spoken in this debate have already referred to them. They have also referred to their own personal experience—the hon. Member for Streatham (Bell Ribeiro-Addy) was one of those who did so—and I think it is always more powerful if we hear about lived experience in any debate and in anything that this House does.

One issue that I want to raise is statutory sick pay. This UK Government must reform statutory sick pay. It disproportionately harms people with disabilities. There has been an argument here today for endometriosis to come under the Equality Act 2010. When people have chronic conditions and have to take time off work, they have to be able to support themselves during that time. The SNP has called continually for statutory sick pay as a minimum to be increased in line with the real living wage, for extending it to 52 weeks instead of 28 and for people to get it from the first day they are sick. This was able to be done during the pandemic; it should be able to be done as we go forward.

We must all continue to raise awareness and fight stigma when discussing menstrual and reproductive conditions, such as endometriosis, in the workplace and in the health sector. I know the difficulties of raising issues in relation to specific illnesses, conditions and diseases—for example, sarcoma, which my husband died of. The issue is getting the medical profession to understand. That is not something that the Government can do directly, but we all can and should raise conditions such as endometriosis frequently, so that information about it gets out there among the general public.

The Scottish Government have a women’s health plan. That aims to take an intersectional approach, recognising that many women and girls in Scotland will face multiple and often overlapping disadvantages and barriers to accessing good healthcare. This UK Government should do something as well. It absolutely is important. I am heartened as an old woman—I am a lot older than I look—when I hear people in the Chamber or here in Westminster Hall discussing the menopause, periods and all these things that were taboo. My late husband was mortified when I was ill and sent him to the chemist to buy me some sanitary towels. This taboo is going, and the further and faster we lose these taboos, the better—especially for women who are suffering.

In Scotland, menstrual health, including endometriosis, is included in the Scottish curriculum, and the Scottish Government have made resources available online for young people, teachers, parents and carers; they are tailored to different age groups. My hon. Friend the Member for Livingston (Hannah Bardell) referred to a video. I sincerely hope that that is one of the things being used, because it is education that will help to end taboos and ignorance.

The Scottish Government are also exploring opportunities to partner with Endometriosis UK and sponsor projects that will raise awareness and support the diverse needs of people living with this condition. They have recently funded an Endometriosis UK project, which will help to increase awareness and support for those awaiting diagnosis. Can I ask the UK Government to do something similar? I pay tribute to Endometriosis UK for all its work, for producing its employer’s guide and for its stalwart work in pushing this agenda forward.

Employment law is reserved to the UK Government, but the Scottish Government will continue to use their fair work policy to promote fairer working practices and to press for the full devolution of employment powers, because we want to do more and we are stymied by the fact that an awful lot of this work is reserved. The SNP’s ambition, shared by the Fair Work Convention, is for Scotland to be a leading fair work nation in 2025. That sits at the heart of the Scottish Government’s ambition to move towards a wellbeing economy and it is central to supporting economic recovery and renewal. As the SNP spokesperson on disabilities, I stand up in many of these debates, and we have to take forward the talents and abilities of people with chronic conditions and disabilities, and use them to the benefit of the entire UK. That is vital.

The Scottish Government have also taken steps to close the gender pay gap through the gender pay gap action plan. That is important, because the condition affects women, and we need to ensure that women are not double, triple or quadruple handicapped by having a chronic condition such as this.

I wish to leave lots of time for the Opposition spokesperson and for the Minister, so I will just say that this UK Government must introduce their much-awaited employment Bill and take forward a progressive agenda for workers’ rights, including a day one right to request flexible working, guidance to employers on reasonable adjustments—which we have heard about—and a statutory timescale for those adjustments to be implemented. Such debates as this are important, consensual though they are. We must all push forward and press for better rights for women who have endometriosis and other chronic conditions.