Earl of Clancarty
Main Page: Earl of Clancarty (Crossbench - Excepted Hereditary)Department Debates - View all Earl of Clancarty's debates with the Department of Health and Social Care
(2 years, 1 month ago)
Lords ChamberMy Lords, I am glad that the noble Baroness, Lady Thornton, asked for this debate, and I applaud her comprehensive introduction. When I asked an Oral Question on this topic on 23 May, I cited a figure of
“1.1 million sufferers of long Covid in the UK … unable properly to undertake day-to-day activities as a result of their condition.”—[Official Report, 23/5/22; col. 656.]
That ONS figure now stands at 1.6 million—the figure is in the excellent Library briefing—and a total of over 1.1 million have been suffering for more than a year, so this is a growing problem. Even though we may be over the worst of Covid as a life-threatening disease, at least for now, a significant minority of those who contract Covid continue to develop long Covid. It is a debilitating illness for the individuals concerned, and its extent represents a wider social problem that the Government need to take seriously.
Many of us know people suffering from this condition, professionally or as friends or relatives. My concern in this debate is what can be done better for those who are suffering, from their own point of view. I thank those with long Covid to whom I have talked about their situation. One friend—under 60 with no discernible underlying conditions, and living in rural Hampshire—contracted Covid in September last year. As symptoms persisted, the GP said that she would be referred to a long Covid clinic in two to three weeks, but that happened only 10 months later, with nothing happening in between. Hers is by no means an isolated case. As the Minister will appreciate, this is not just about the waiting time to get to a clinic, crucial though that is; it is also about what happens up to that point. So I ask him: what is being done to help upskill all GPs, and what can be done as soon as a patient contacts a surgery? What can be done to better signpost the support that a patient requires at an early stage? Indeed, what can be done to ensure that those who have long Covid or suspected long Covid contact a GP in the first place?
My friend tells me that, ideally, the GP should have said, “Stop work completely. I’ll fill in a sick note. Come back in four weeks and we’ll keep an eye on you”. This is with hindsight, of course. She believes that, if she had been set on the right road and been monitored from the off, she would be much further down the road to recovery. She would also have missed much less work. As it is, over a year later, she can still do at most only two days of work a week.
Her main symptom is fatigue, in line with 70% of the 1.6 million that I have cited. This is not just about not being able to climb a hill; it is about not having any energy to do anything for a period of time. Of course, many people’s stock reaction to this, sufferers and non-sufferers alike, is “Carry on regardless, try to take more exercise”—one very good reason why long Covid should be treated professionally as quickly as possible.
Additionally, addressing these concerns will avoid in toto a significant loss to the economy, as others have pointed out. The Government need to take a significant note of that. There must be faster access to long Covid clinics, as the noble Baroness, Lady Thornton, said. Clearly there is still a postcode lottery about referral. Many more clinics need to be put in place across the whole of the UK, to decrease waiting times and to ensure that everyone has the same level of access, which continues to vary hugely across the country.
Fortunately, my friend now has a case manager, a qualified physiotherapist who can refer her to different services according to the symptoms displayed. We know that a multitude of symptoms are exhibited by sufferers, so there is the respiratory team, the occupational therapy team and so on. The problems do not stop there, though, in terms of delivery, because there are also difficulties in accessing those services, as has been pointed out. Can that be looked at, as well as the priorities over access and the funding involved for long Covid patients? One good thing in my friend’s case is that meetings with her case manager are through Zoom. Travelling is very difficult for long Covid patients.
Such is the demand for treatment and the slowness of NHS provision that there are now heavily subscribed private online programmes of treatment. People are desperate but there is a question over whether these services are a substitute for those services referred through the NHS as part of what, ideally, should be a complete and integrated programme of recovery. I say this as an open question.
In an informative video on YouTube, one sufferer, Gez Medinger, sums up what many sufferers experience when he says, “It takes every aspect of your life and pretty much crushes it”. The Government need to do as much as possible to support those with long Covid, as well as putting money into research to beat this condition.