Humber and North Yorkshire Health and Care Partnership are inviting current and former smokers, living across our region, to take part in a confidential survey designed to find out how they feel about smoking and the support available to quit.
The information gathered by the survey will be used to inform communications as Tobacco Dependence Treatment Services are launched in NHS Trusts in the coming year, to support Smokefree hospitals, in line with the long-term plan. The survey, which closes on Friday 20th May 2022, takes just 5 minutes to complete and those who do it will be entered into a prize draw to win a £40 Love to Shop voucher.
If you’re a current or ex-smoker, you can take part in the survey here. Or, you can share the link with friends, family, patients and colleagues to help the Partnership gather the widest possible data set.
A social media campaign supporting the survey is running. You can help spread the word by sharing posts. Follow the Cancer Alliance on Facebook and Twitter for updates.
The latest edition of Cancer Alliance stakeholder newsletter is now available.
This edition includes updates from across the Cancer Alliance and leads with the announcement of the Cancer Alliance’s rebrand to Humber and North Yorkshire Cancer Alliance. Click here to read the newsletter
Allyson lives in the East Riding of Yorkshire and began her career in the NHS at the age of 17. After retiring in 2018, Allyson noted that she had ‘never really been ill’ until she was diagnosed with breast cancer after attending a breast screening appointment in 2019.
Here you can read what happened after her diagnosis and how she is now helping to support others receiving personalised care.
“My breast cancer was identified during a breast screening appointment. Following my diagnosis, I underwent surgery and 15 sessions of radiotherapy.
“After finishing up treatment for breast cancer, I wanted to do something to raise money for Breast Cancer Now, so I applied to do The Moonwalk in London (walk 26.2 miles at night!).”
In December 2019, Allyson was training for the Moonwalk event and walking two miles a day but despite regular exercise, Allyson had started to notice that she was putting on weight around her stomach and in March 2020, she also started experiencing stomach pains.
“I spoke to my GP and one of my prescribed drugs, which prevented osteoporosis (a potential side effect of breast cancer) had recently changed from a branded product to the generic drug, so we thought this may be the cause. Since it was the start of the pandemic, seeing a GP for a stomach ache didn’t feel appropriate, but it only got worse over the next few weeks and by May 2020, I looked five months pregnant. I decided to contact my GP again and this time I was booked in for a face-to-face appointment.”
Allyson’s GP submitted a referral for an urgent scan however, two days later her symptoms had become worse so she returned to the GP and was admitted to hospital for a CT scan. Whilst in hospital, Allyson had six litres of fluid drained and five days later she was told that she had ovarian cancer.
“I was very weak and frightened. Following an MRI scan, it was decided I would have four sessions of chemotherapy and in September 2020 I underwent surgery.
“When I was diagnosed, I didn’t know the symptoms of ovarian cancer but I’d encourage women to familiarise themselves with B.E.A.T.
“As women, we tend to accept stomach pains and bloating but it’s important to understand what’s normal and speak to your doctor if you’re experiencing symptoms that don’t seem right.”
Coming to terms with a cancer diagnosis
“Receiving the ovarian cancer diagnosis was devastating for me and my family. It felt like being woken up in the middle of the night and thrown into the ocean without a life raft. I was so frightened and all I could think about was my death. I felt so alone.
“My husband became my carer and made sure I was eating and drinking properly. After a few months, I started to feel stronger physically and mentally and wanted to take back some control. I began looking at my diet and exercise, as well as investigating ways to manage my mental health.
“Women with ovarian cancer are three times more likely to develop mental health problems and I knew I was struggling. Thankfully, I found Ovacome, an ovarian cancer charity that supported me in my time of need.
“Through Ovacome, I met other women with a diagnosis who have since become dear friends that I couldn’t have managed without. I was a strong, independent woman when I was diagnosed with cancer for the second time, but it made me feel vulnerable, yet determined to do something to help myself and other women with a diagnosis.”
“I knew I needed to get fit for surgery and to help with the recovery after, so when I saw a challenge to run 60 miles for Cancer Research UK, I decided to try and walk it instead. I started to walk again, albeit slowly on some days following the chemotherapy. I was very weak, but feeling the weather on my face made me feel so much better.
“In the month prior to my surgery, I walked 70 miles. It wasn’t easy but I was determined to be as fit as I could be. In the month after surgery, I’m proud to say I walked 26 miles and have continued to walk every day since, whatever the weather.
“Walking has been my salvation. As I came to the end of my chemotherapy treatment, I set a goal of walking 1000 miles in 2021.
“When I realised I was walking a marathon a week, my goal changed to 52 marathons in 52 weeks. Sometimes I’d walk with my husband, other days alone, in silence, listening to the sound of each step like a sort of meditation.
“There were other times where I struggled, too, usually because of the ‘scan anxiety’ common among women like me. Slowly, I learned to face my fears. One day I loudly sang Gloria Gaynor’s I Will Survive while sobbing, which helped with my ‘I can do this!’ attitude. Luckily, we live in the countryside, so nobody saw me!
Walking together
“During one of my walks, at a time when I was receiving lots of messages of support from others, I came up with the idea of creating a virtual walking group for women with ovarian cancer. I got in touch with Ovacome, who had helped me previously, and we created the Walk With Me group.
Walk With Me is a friendly and supportive group that helps people with Ovarian cancer to achieve their individual walking goals. The group connects virtually on WhatsApp to share friendship, encouragement, stories, and photos of the wonderful things they see on their walks. We also have a Strava club where people can share their routes and congratulate each other.
“Walk With Me isn’t about the distance; it’s about supporting each other through ovarian cancer and sharing our experiences. With the support of the women in the group, I achieved my goal and walked 55.3 marathons in 52 weeks. That even included a few weeks with plantar fasciitis, but nothing was going to stop me!
“I now only do things that bring me joy every day and walking has become that for me, I face my fears as they arise, but know whilst cancer has changed me, it does not define me, but has been a real opportunity for change in my life for which I am grateful.”
The NHS wants to hear from children and young people, and their families, about their experiences so it can continue to improve the care and services.
A diagnosis of childhood cancer understandably has a devastating impact on the emotional health and wellbeing of the child and their family, both during and after treatment. Children and young people’s treatment and experience of cancer differs greatly from adults and we recognise the need for a personalised approach to their cancer care.
It’s so important for us to listen and learn from children and young people in order to provide them with the best possible care and experience throughout treatment and to reduce the impact it has on them later in life.
The Under 16 Cancer Patient Experience Survey will inform how the NHS delivers cancer services with the aim to radically improve the outcomes for children and young people affected by cancer.
If you receive an invitation in the post please complete the survey.
Andrew Markham, a Warehouse Operative from Brigg, was diagnosed with prostate cancer when he was 63. After receiving treatment in November, Andrew is now sharing his experience to encourage other men to become more aware of their risk, which can result in an earlier diagnosis.
Andrew (right) is passionate about fundraising for prostate and pancreatic cancer charities.
“In my late 50s, I had a problem with my tummy. I decided to speak to my GP about it, who asked me if I’d ever been tested for prostate cancer. Thinking back, I hadn’t, and so I went along for a PSA test*. After a slightly nervous wait, the results came back at just over four, which is a little high, but not necessarily a huge concern.
“Because my PSA was slightly high, I went back for a PSA test every six months after that. It always fluctuated between 3.9 and 4.2 and therefore seemed okay. This was until one test, when I was 63 in December 2020, which showed, despite a lack of any other symptoms, my PSA had gone up to 4.6, so the consultant suggested I have an MRI. I wasn’t too concerned, as my urologist assured me it was a precaution and my PSA still wasn’t very high.”
*A PSA test is a blood test to measure the amount of a prostate specific antigen (PSA) in the blood. PSA is a protein produced by normal cells in the prostate and by prostate cancer cells. It’s normal to have a small amount of PSA in the blood, and this even rises as men age because the prostate increases in size. A high PSA level can be an indicator of cancer or another problem with the prostate. Regular PSA testing can help GPs spot a problem early, even if there are no other symptoms.
“In May 2021, I received an MRI scan at Scunthorpe General Hospital. When attending my results appointment with a urologist, they said they’d found a lesion on my prostate and that it was best to investigate it further.
“I was then booked in for a biopsy, again at Scunthorpe General Hospital. My appointment took the full morning and I had 15-20 samples taken, but my wife Jenny and I were given plenty of cuppas – the nursing staff were brilliant. Two weeks passed and the results came – I had cancer. On the day of my results, my workplace has asked me to take part in a fundraiser for Men’s Health Week as they knew I fundraise for pancreatic cancer charities. It was ironic to receive the results I did.
“Later, another biopsy appointment confirmed a large tumour, bigger than I and they expected, and I was given a full diagnosis at the end of September 2021. My tumour was stage one with a Gleason score of 7.
“There are several options for treatment when it comes to prostate cancer, and I was given a choice between radiotherapy, hormone treatment, or surgery. After speaking with Jenny and some friends at a Brigg fundraising group, I decided to have surgery to remove the tumour.
Andrew (left) and a friend fundraising for Prostate Cancer UK.
“On 28th November, I had a robotic-assisted laparoscopic prostatectomy (RALP) and have been recovering since then. I’m still tired, in pain, and have been off work for six months now, but I’m happy to have found my prostate cancer and had the procedure. In two weeks, I’ll be going for another CT scan to see if there are any other problems underlying.
“Although prostate cancer isn’t nice, knowing your risk and contacting your GP if concerned can help you get an earlier diagnosis. Men who are black or who are aged over 50, like I was when I was diagnosed, are most at risk. Knowing your risk is important, as it can help you and your GP decide whether you should be monitored or undergo tests, such as a PSA test, for prostate cancer.
“Prostate cancer doesn’t always have symptoms, but Prostate Cancer UK’s risk checker can help you determine your risk in 30 seconds. I’d encourage all men to use the risk checker and contact their GP if they have a higher risk.”
April is Bowel Cancer Awareness Month, a fantastic annual opportunity to raise awareness of the fourth most common cancer in the UK.
Bowel cancer is also the UK’s second biggest cancer killer, however it shouldn’t be because it’s treatable and curable especially if diagnosed early.
Nearly everyone survives bowel cancer if diagnosed at the earliest stage but this drops significantly as the disease develops. Early diagnosis really does save lives.
That’s why we’re supporting Bowel Cancer Awareness Month and Bowel Cancer UK, the UK’s leading bowel cancer charity, to raise awareness of the symptoms of bowel cancer:
Bleeding from your bottom and/or blood in your poo
A persistent and unexplained change in bowel habit
Unexplained weight loss
Extreme tiredness for no obvious reason
A pain or lump in your tummy
Most people with these symptoms don’t have bowel cancer. Other health problems can cause similar symptoms. But if you have one or more of these, or if things just don’t feel right, see your GP.
For more information about bowel cancer and details of how to get involved in Bowel Cancer Awareness Month visit www.bowelcanceruk.org.uk
Humber, Coast and Vale Cancer Alliance has been renamed as Humber and North Yorkshire Cancer Alliance, effective from today (Friday 1st April).
The Cancer Alliance has changed its name to align with our local integrated care system (ICS), the Humber, Coast and Vale Health and Care Partnership, which has been renamed as the Humber and North Yorkshire Health and Care Partnership from today.
ICSs are partnerships of health and care organisations, local government and the voluntary sector. They exist to improve population health, tackle health inequalities, enhance productivity and help the NHS support broader social and economic development.
Subject to Parliamentary approval, ICSs will be put on a statutory footing from Friday, 1st July 2022, and will operate in shadow form for the next three months.
The ICS identity change also includes a branding refresh (new logo and brand colours). Subsequently, the Cancer Alliance has also adopted a new logo and the new ICS brand colours.
As part of this refresh, the Caner Alliance website address and social media channels have also changed. These are now:
Tuesday 15th March is National Cancer Clinical Nurse Specialist awareness day. We are supporting the #NationalCancerCNSday campaign to help shine a spotlight on the role which is often referred to as a lifeline for patients and their families. Here you can meet some of the CNS’s that are helping to care for people affected by cancer across Humber, Coast and Vale.
Louise Salt
Louise Salt
Colorectal/Stoma Clinical Nurse Specialist,
Diana Princess of Wales Hospital
How long have you been in the NHS?
I have worked for the NHS for 41 years.
Why did you want to join the NHS?
I love and am very interested in people. Everyone has a story and different life experiences that makes them who they are. It is a pleasure and privilege to help/assist them and their families when they need medical help. I believe access to a great health service and care should be available to everyone regardless of means, that is why I choose to work for the NHS rather than the private sector.
What does your role involve?
At present I help with the five year follow up of patients who had bowel cancer. I also see patients and their families at cancer diagnosis, surgery and throughout the journey of having had or living with bowel cancer. Also I do some work with patients who have had or having a stoma.
What is the best part of your job?
It is always having contact with patients and their families, I am also fortunate to work as part of the colorectal team who I believe are brilliant and share the same ideals as me of giving the best care we can and aiming for the best outcome and experience for the patient and their families facing a difficult time.
What does caring for people affected by cancer mean to you?
The word cancer still naturally conjures up imminent or impending death for most people. Part of my role is helping people to adjust to having a cancer diagnosis and explaining how we can, in a lot of situations, attempt to rid them of it completely. My role involves supporting people to continue living their lives and finding normality in everyday life. The family and friends around them give the majority of support, but we are also there to help when needed.
Vicky Dixon
Vicky Dixon Haematology Advanced CNS at York and Scarborough Teaching Hospitals NHS Foundation Trust
What is the best part of your job? The best part of my job is helping people cope through and with very difficult situations. Helping and caring for people with cancer gives you a constant sense of perspective and a strong belief and strength in the power of kindness and compassion.
Lynne Buckley
Lynn Buckley
Macmillan Gynae-Oncology Clinical Nurse Specialist and Advance Nurse Practitioner,
Hull University Teaching Hospitals NHS Trust
How long have you been in the NHS?
I have worked in the NHS for 37 years.
Why did you want to join the NHS?
It’s hard to remember that long ago, but my mum was a nurse and I followed in her footsteps.
What does your role involve?
I support women and their families through cancer diagnosis, treatments and beyond. Every day is different, most days involve breaking bad news, managing expectations, ensuring that women have the information they need to be able to make decisions about their care and that their holistic needs are met. I work closely with a much wider team of health care professionals across multidisciplinary and multiservice boundaries. I also contribute to developing services and guidelines.
What is the best part of your job?
Knowing that you have done your best for that person in front of you and they feel valued and that their needs have been met.
What does caring for people affected by cancer mean to you?
I feel privileged to be part of the cancer pathway and hope that my input has made things a little easier for people affected by cancer.
Claire Wise
Claire Wise Gynaecology Clinical Nurse Specialist at York and Scarborough Teaching Hospitals NHS Foundation Trust
What is the best part of your job? “The best part of my job is being the constant for someone and building supportive relationships.”
Developed with clinical leaders, the proposals – supported by NHS staff as well as patient groups and cancer charities – aim to simplify and update cancer standards, based on the recommendations of the Independent Cancer Taskforce.
Patients, clinicians and the public will be asked to share their views on the proposed standards over the next month, with a report setting out the changes published today.
Cancer currently has a complex set of nine separate performance standards, with different targets covering different routes into the system, for example, screening or a GP referral.
The new plan proposes ensuring patients have the same opportunity for faster diagnosis and treatment, including:
The 28-day faster diagnosis standard, which would see patients who have been urgently referred, have breast symptoms, or have been picked up through screening, have cancer ruled out or receive a diagnosis within 28 days.
A 62-day referral to treatment standard, meaning patients who receive a cancer diagnosis will start treatment within nine weeks from the date of referral.
A 31-day decision to treat to treatment standard, so that cancer patients receive their first treatment within a month of a decision to treat following diagnosis.
These new standards aim to make diagnosis and treatment timelines easier to understand for people with suspected cancer and their families, while also helping to diagnose cancers earlier and save more lives.
Before the faster diagnosis standard was introduced, access standards for cancer have remained unchanged since 2009. The current two-week wait target sets no expectation of when patients should receive test results or actually get a confirmed diagnosis.
Cancer care has been prioritised throughout the pandemic with the latest data showing the number of people getting checked for cancer increased by over half a million (512,110) in one year between December 2020 and December 2021.
In December alone, there were over 215,000 urgent referrals for cancer and more than nine out of 10 people started treatment within one month.
Dame Cally Palmer, NHS National Director for Cancer said: “Access standards have been key to improving timeliness of treatment for people with cancer since they were first introduced in 2000.
“As we see advances in diagnosis and treatments for cancer, it is only right that these standards are modernised – so that we can ensure patients are diagnosed more quickly and are given the treatment they need as soon as possible, helping us save even more lives.
“These proposed changes are an important part of improving cancer care and so from today, the NHS will be inviting views from patients, staff and the public”.
Professor Peter Johnson, National Clinical Director for Cancer for NHS England, said: “We know that people having tests for possible cancer want to know the results quickly, and updating the standards to reflect this will help us to make sure we are able to deliver the best possible care.
“We are encouraging colleagues in NHS cancer services to share their views on the consultation to ensure we have standards that are better for people with cancer”.
Health and Social Care Secretary, Sajid Javid said: “As part of our 10-Year Cancer Plan, we want to offer patients the best possible care and treatment.
“These proposals will help us speed up diagnosis times and treatment, and save more lives.
“The NHS wants to hear from as many people as possible – and is seeking advice from patients, staff and the public. Please, make your voices heard”.
Under the new proposals, the NHS would focus on the time from referral to people finding out their results within a maximum of 28 days. This faster diagnosis standard has a clearer focus on measuring and incentivising early diagnosis, rather than just time to first be seen.
Areas where the new standards have been tested have shown that performance against the 62-day referral to treatment standard was significantly higher (74.9%) than the control group (71.7%) when using the new measures.
Proposals are in addition to the target announced in the elective recovery plan, published last month, which outlined the NHS aim to return the number of people waiting more than 62 days from an urgent referral back to pre-pandemic levels by March 2023.
Catherine Harper-Wynne, Chair of the Breast Cancer Faster Diagnosis Group, said: “The proposed update in standards provides a better reflection of our current clinical approach and allows for greater flexibility to offer patients the most efficient route to diagnosis, allowing us to start treatment as quickly as possible. For breast cancer patients, there is evidence, from the pilot already completed, that a higher proportion of patients had cancer ruled out within 28 days”.
Jane Lyons, CEO of charity Cancer52, said: “People with rare and less common cancers often have vague symptoms and it can take longer for their cancer to be diagnosed. So a commitment to a diagnosis in 28 days for all cancers, including those that are more challenging to diagnose, is a good step forward. Earlier diagnosis can mean more people start treatment sooner and more lives will be saved, and we support work to help the NHS meet its ambitions to diagnose more cancers faster and earlier”.
Patients have told the NHS that the focus on achieving a rapid diagnosis or ruling out of cancer is the right one, and is more meaningful to patients than the timing of a first appointment.
A new campaign taking a radically different approach to detecting cancer early for patients, when it is easier to treat, has been announced today by NHS chief executive Amanda Pritchard.
Running across TV, radio, and social media from tomorrow, the campaign is the first to focus on tackling the fear of cancer rather than specific symptoms.
The key message is that if you think something is wrong it is always better to get checked out to put your mind at rest, or to get treatment that maximises your chances of a good outcome.
The NHS Long Term Plan committed to increasing the number of cancers detected at an early stage one or two from half to three quarters by 2028.
NHS staff have been checking record numbers of people for cancer. Latest figures show that the number of people getting checked for cancer increased by over half a million (512,110) in one year between December 2020 and December 2021.
Speaking ahead of the launch, NHS chief executive, Amanda Pritchard, said that people should continue to come forward for these vital checks, adding that it was important for people to try to set their mind at ease if they have worrying symptoms by getting checked without delay.
It comes alongside new research showing that nearly six in 10 people (56%) say a cancer diagnosis is their biggest health fear, above other illnesses including heart disease and Covid-19.
Almost two thirds (63%) of those surveyed said dying was their biggest cancer fear, with more than one in three (37%) worried about being a burden on family and friends and over another third (36%) worried about the impact of chemotherapy or other treatments.
While the majority of people knew catching cancer earlier makes it more treatable, over two fifths (42%) said they would ignore symptoms, wait to see if anything changed, look for answers online or speak to family and friends before seeing their GP.
Launching officially on Wednesday, a new advert will show a man who is worried about his symptoms carrying a jack-in-the-box around with him, which he winds up as he goes about his day. When he eventually gets checked and discovers he doesn’t have cancer, a consultant opens the jack-in-the-box to show it is empty.
NHS bosses and cancer charities are urging people not to delay “lifesaving” checks, highlighting nine in ten of those checked turn out not to have cancer but that it is better to know so that people can get treated early when chances of survival are highest.
NHS chief executive, Amanda Pritchard, said: “We know that the prospect of a cancer diagnosis can be daunting for people and that is exactly why we are launching this potentially lifesaving campaign – we want to allay people’s fear about cancer and encourage them to get checked without delay.
“We know that many people don’t want to burden or bother anyone with their health concerns, but we would always prefer to see you sooner with a cancer that is easier to treat, than later with one that isn’t.
“NHS staff have pulled out all the stops to ensure cancer was prioritised throughout the pandemic with over half a million people starting treatment over the last two years and record numbers of people now being referred for checks and tests.
“So, the NHS is here for you – don’t let cancer play on your mind – get checked without delay.”
NHS cancer director, Dame Cally Palmer, said: “Despite cancer remaining a priority during the pandemic, with referrals at record levels for more than 10 months and more than half a million people starting treatment in the last two years, we have seen fewer people than expected come forward for lifesaving checks which is why were are launching this campaign – the first of its kind – that looks to tackle people’s worries head on and support earlier diagnosis.”
“The fear of cancer is completely understandable but please don’t let worries and concerns about treatment or potentially bad news prevent you from coming forward – and help us to help you.”
NHS clinical director for cancer, Professor Peter Johnson, said: “A key part of this new campaign is encouraging people to be aware of any changes in their body, and not to hold back from getting them checked.
“Most people who come forward and get tested for cancer find out they don’t have it, but whatever the result, the NHS wants you to know that we are here for you and finding out sooner is always better.
“It might be nothing at all, it might be something else the NHS can help you with, but if it is cancer then finding it early makes it much more treatable, and it could save your life.”
Phil Kissi, 64 from London who has recovered from prostate cancer, said: “In 2006, I was watching a TV programme that said Black men were at higher risk of prostate cancer. Although I didn’t have any symptoms, I had a feeling that something wasn’t right.
“My diagnosis changed my perspective on life, and I re-evaluated what was important to me. After my surgery, I decided to go into athletic training and help young people who might not have had the chance to fulfil their potential otherwise.
“If you’re worried about cancer, contact your GP practice. It’s probably nothing serious but even if it is, getting your diagnosis earlier can give you more treatment options and ultimately, a better chance of success.”
Dr Ian Walker, director of policy, information, and communication, at Cancer Research UK, said: “Sometimes a little bit of concern or fear about our health can prompt us into action, but it’s vital that this fear doesn’t get to a level that stops us picking up the phone or walking into the surgery.
“We’ve spoken to a lot of people who’ve noticed changes to their health but weren’t sure what to do, or needed help with the next steps. We encourage anyone in this situation to get in touch with their GP practice. They have nothing to lose but could have everything to gain because finding cancer at an early stage can make all the difference.”
Dr Anthony Cunliffe, Clinical Adviser for Primary Care at Macmillan Cancer Support, said: “People might put off seeing their doctor if they’re worried that their symptoms could be cancer – the specially trained nurses and advisors on Macmillan’s support line often hear about the toll a potential cancer diagnosis is taking on their mental health. But, for most people, there’s another explanation for their symptoms.
“However, we know that early diagnosis of cancer can improve prognoses and save lives, and anyone worried about potential cancer symptoms should contact their GP as soon as possible. Don’t think it’s not important or put it off. Your GP will make time to listen to your concerns.”
Jane Lyons, CEO of Cancer52, which works with charities supporting people with rare and less common cancers (you can find a list of these on www.cancer52.org.uk), said:
“Worrying about having cancer is completely understandable and getting checked out a scary experience, so it is good to know that nine out of ten people who do come forward don’t have cancer.
“But if you are one of the people who does have a cancer, especially a rare or less common cancer where symptoms might not be so obvious or well known to people or health professionals, then it is usually better to get an earlier diagnosis where there can be more treatment options and better outcomes.
“And with rare and less common cancers, which account for more than half of cancer deaths in England, it can take more persistence and more visits to GPs to get an accurate diagnosis so it’s even more important to get in touch if you think something is wrong.”
Cancers are much more likely to be treated successfully if caught at an early stage.
More than nine in 10 bowel cancer patients will survive the disease for more than five years if diagnosed at the earliest stage. Similarly, 92.8% of women diagnosed with the earliest stage ovarian cancer survive the disease for at least five years compared to around 13.3% for women diagnosed with the most advanced stage of the disease.
Not all the symptoms of cancer are easy to spot. The NHS is encouraging people to contact their GP practice if they experience any of the below symptoms:
Tummy trouble, such as discomfort or diarrhoea for three weeks or more, or
Blood in your pee – even just once;
Unexpected or unexplained bleeding;
Unexplained pain that lasts three weeks or more;
An unexplained lump; or
A cough for three weeks or more (that isn’t COVID-19).
Other signs and symptoms to prompt contact to your GP practice if experienced for three weeks or more include:
