
Doctors dismissed my common cancer symptom as ‘hormones' for 2 years – now I'm riddled with incurable tumours
Click to share on X/Twitter (Opens in new window)
Click to share on Facebook (Opens in new window)
FOR years, doctors told Lea Hughes that her common cancer symptom was simply caused by hormones - now she has tumours in her liver, bones, brain and lungs.
The 38-year-old first spotted a small lump on her right breast when she was 29, but was reassured her "lumpy boobs" were just due to hormones.
Sign up for Scottish Sun
newsletter
Sign up
13
Lea Hughes, 38, first went to doctor about a lump in her breast when she was 29
Credit: SWNS
13
She was dismissed as having lumpy boobs due to hormones but three years later it had grown
Credit: SWNS
13
Lea was dismissed with stage 4 breast cancer that was incurable
Credit: SWNS
But two years later, she spotted the lump had become a "dimple".
This time, doctors instantly referred her for an immediate mammogram, ultrasound and biopsy.
Lea was told she had stage four breast cancer and, in the years the cancer had been missed, it had spread to her liver and bones.
Confronted with an "incurable" diagnosis, Lea tried tried a range of medications, therapies, and treatments to stabilise her cancer and prevent it spreading further.
This seemed to work until August 2024, when a scan showed it had infected her brain.
In March this year, she learned the cancer was in her lungs too.
Lea, from the Wirral but living in Leytonstone, East London, has now exhausted NHS-funded options and is fundraising for private care.
She's hoping to raise enough money to access a targeted cancer drug called Enhertu, which isn't available on the NHS for people with Lea's diagnosis.
In clinical trials, the drug added months or even years to the lives of women with incurable breast cancer that had spread, but the National Institute for Health and Care Excellence (NICE) last year decided not approve it for the NHS on value for money grounds.
Lea, a former fashion and retail marketer, said: "When the doctor first told me I had lumpy boobs, I'd never heard of it before.
Jessie J breaks down in tears in heartbreaking hospital video as she has surgery after breast cancer diagnosis
"But years on, I saw the lump had grown when I was putting a bikini on and I spotted a shadow caused by the lump.
"Within weeks, I was diagnosed with stage four incurable cancer aged 31.
"Treatments contained it - until August 2024 - and now it's in my brain and lungs too.
"I know the doctors and nurses so well now, after seven years at St. Bartholomew's Hospital, London.
"It's longer than any relationship I've ever had."
13
Lea was able to keep the cancer under control until last year
Credit: SWNS
13
Scans showed the cancer had spread from her bones and liver to her brain
Credit: SWNS
13
Lea Hughes in hospital during radiotherapy treatment
Credit: SWNS
Lea first noticed her small lump on the front of her right breast in 2015 and went to the doctor to get it checked out.
But she says they told her she just had "lumpy boobs" and as she was only 29, with no family history, she didn't qualify for further testing.
She tried to raise it several times afterwards but says it wasn't until a holiday in early 2018 that doctors were prompted to act.
She said: "I was putting a bikini on and I saw a shadow and a dimple.
"When I explained it on the phone, they referred me straight to the hospital.
I have no choice just to get on with it and keep fighting
Lea
"I went for a mammogram and an ultrasound, then a biopsy.
"When it came back as cancer, they did a breast MRI scan and noticed a shadow on my liver in the corner.
"So they did full body scans - MRIs, PETs and bone scans - and learned it had spread to my liver and bones.
"I was diagnosed with stage four incurable cancer in a matter of weeks in April 2018 on Friday 13th, of all days."
13
Lea receiving cancer treatment in hospital
Credit: SWNS
13
Lea wearing a cold cap during chemotherapy treatment
Credit: SWNS
13
The 38-year-old had to have her lung drained in hospital, after the cancer spread to her lung
Credit: SWNS
Lea was put on several treatments at St. Bartholomew's Hospital in a bid to stabilise and contain the cancer.
In June 2022, she had a single mastectomy.
Then one of the oral therapies made her so unwell that she ended up hospitalised in August 2023.
She said: "I had hypercalcaemia - high calcium levels in the blood - and needed multiple blood transfusions.
"It felt very real - I realised that this illness really could take me out."
What are the signs of breast cancer?
BREAST cancer is the most common type of cancer in the UK.
The majority of women who get it are over 50, but younger women and, in rare cases, men can also get breast cancer.
If it's treated early enough, breast cancer can be prevented from spreading to other parts of the body.
Breast cancer can have a number of symptoms, but the first noticeable symptom is usually a lump or area of thickened breast tissue.
Most breast lumps aren't cancerous, but it's always best to have them checked by your doctor. You should also speak to your GP if you notice any of the following: a change in the size or shape of one or both breasts
discharge from either of your nipples (which may be streaked with blood)
a lump or swelling in either of your armpits
dimpling on the skin of your breasts
a rash on or around your nipple
a change in the appearance of your nipple, such as becoming sunken into your breast
Source: NHS
Instead, Lea went on IV chemo for 10 months, which got the cancer under control.
But a routine scan in August 2024 showed her liver tumours had began to progress.
Doctors did a full-body scan to see if she would be eligible to join a new trial, but it found that the cancer had spread to her brain too.
Lea said: "It's one of those things, with stage four breast cancer, you know it can spread to the brain and you do worry.
"But I didn't expect it then, because I had no symptoms at all."
'Not giving in'
In September 2024 she started whole-brain radiotherapy, followed by another round of IV chemotherapy.
Then she had radiotherapy on her spine - but her body was so weak that it started to "give up" in December 2024.
She said: "I'm 5ft 10ins and I went down to 7st.
"I was too weak to hold myself up - I was watching myself waste away.
"I had to shave my head when I started losing my hair too.
"I didn't recognise myself and seeing those changes was very confronting."
Lea began having breathing issues in March this year. The cancer had spread to her lungs and she had 4.5 litres of fluid drained from them.
Now Lea is on her sixth course of chemotherapy.
She is fundraising to pay for Enhertu - which is available on the NHS for some breast cancers, but not Lea's.
13
This is because her cancer has spread extensively, including to her brain.
But she believes it could potentially be effective for her brain cancer too, because Enhertu crosses the blood-brain barrier - which not many chemotherapies do.
In a trial undertaken by its developers - AstraZeneca and Daiichi Sankyo - six in 10 women with incurable cancer saw their tumours shrink after being given Enhertu.
However, without NHS funding, it can cost over £10,000 per cycle.
Lea said: "I always try to lean into the positive - accepting how sh***y this is, but also not giving in.
"But it does feel very real when things don't work.
"I can't believe everything I've been through - you don't realise until you sit back and reflect.
"But I have no choice just to get on with it and keep fighting."
You can contribute to Lea's fundraiser here.
13
Lea has now exhausted all NHS funded options
Credit: SWNS
13
She's fundraising to access the drug Enhertu privately
Credit: SWNS

Try Our AI Features
Explore what Daily8 AI can do for you:
Comments
No comments yet...
Related Articles


Telegraph
40 minutes ago
- Telegraph
I'm a palliative care doctor – the new assisted dying Bill puts the vulnerable at risk
Prof Mark Taubert is a palliative medicine hospital consultant and clinical director at Velindre University NHS Trust. He is also a professor at Cardiff University School of Medicine and chair of the advance and future care planning group at NHS Wales. As I watched the Terminally Ill Adults Bill on Friday, one moment struck me very hard. An amendment was being voted on by MPs. This amendment would ensure that someone 'substantially motivated' by feelings of being a burden, a mental disorder, a disability, financial considerations, lack of access to treatment, or suicidal ideation would not qualify for assisted dying. It was voted down. At this point, I knew the House of Commons would vote with a majority for this assisted dying legislation. Legislation I do not feel is good enough. And it was a slim victory, but passed it was. The reality of my patients Perhaps I should explain with some practical examples, regarding people whose details I have substantially changed to preserve anonymity. I have a patient who is his mid-40s. He has suffered from alcoholism and substance abuse for much of his adult life and is facing a custodial sentence. He has attempted suicide on four occasions, and he now has prostate cancer. In addition, he has Type 2 diabetes, and also a chronic lung condition which makes it harder for him to breath. Another patient has stage 4 breast cancer and is 25 weeks pregnant; she is facing being evicted from her home, has an abusive partner and also a history of self-harm and anorexia nervosa. Offering these individuals assisted suicide (even amongst many other potential other options) does not feel like the right approach; in fact, it will very likely be misconstrued. Assisted dying may to some seem like a solution to all their challenges. A form of treatment, although many would contend that it is anything but. If we as clinicians start approaching it from such an angle, and mention this option as one amongst many 'treatment' options, will they just assume that 'doctor knows best', and go ahead? Not all patients are strong independent people Those working in politics in recent weeks seem to have been working under an assumption that patients have an advanced cancer in isolation from other conditions, that they are all strong, independent people, like those appearing in the advertisements by the pressure group Dignity in Dying. In Kim Leadbeater's proposed assisted dying legislation, the premise appears that the issue is simple – just give people the choice! Much of the assisted dying debate we have heard focusses on patients with advanced cancer, with 'less than six months to live', who wish to die early. But clinicians like me have been frustrated at the lack of understanding about the complexity our patients face; for example, the ones I have just mentioned. They often live with multiple conditions and separate issues. Six months or less is, more often than not, guesswork. In the real world outside of Westminster, which I see daily in hospitals, outpatient clinics and in the community, patients have multiple long term illnesses and other morbidities simultaneously. I regularly see patients who have a stage 4 cancer, but are also in a wheelchair; have had severe mental health issues including bipolar disorder and severe depression in the past; have attempted to take their own lives multiple times well before their cancer diagnosis; live in poverty; are facing homelessness and often feel devalued, due to a co-existing disability. An additional diagnosis like prostate cancer or breast cancer may then become their 'key to access' the assisted suicide clinic; or may be used by a person controlling them as a way to gain access, and rid themselves of the individual. What we have is a complex patchwork of patients with various, distinct needs, yet politicians are still debating this as though we can compartmentalise and separate these conditions neatly, quite separate from the patient. It's simply not the case. Promises to make the Bill bulletproof and safe don't seem to have happened Despite evidence from other areas of the world where assisted dying is legal, our political class – seemingly to honour a promise to a celebrity – blunder ahead with a pass-it-now-and-we'll-sort-out-difficulties-later attitude. Don't worry, the House of Lords can fix any of the flaws and then the Secretary of State can add on bits later, too. It seems to me that at its second reading, back in November, similar promises were made to make the Bill bulletproof and safe by its third reading, but that does not appear to have happened. Clinicians like myself struggle to understand how amendments to this Bill, that might protect vulnerable groups – such as those with dementia or Down's Syndrome, or those suffering from eating disorders – have been rejected one by one. Establishing why someone wishes to take their own life, and asking whether an advanced cancer diagnosis really is the main trigger, and whether or not someone might change their mind, will be hard, even for the most experienced clinicians. What exactly is going on? There is a blinkered mentality among some who do not wish to see the issues in anything but simple terms, with columnist and peer Lord Finkelstein being a prominent example, but you also wonder how much influence extremely well-funded pressure groups like Dignity in Dying have exerted in all of this. I would hazard a guess that Assisted Dying clinics of the future will have pink signage. This Bill promises to make very difficult decisions much more straightforward and clear. But life is not straightforward and it is the vagueness of the Bill – with its huge number of unanswered questions – that concerns those at the coalface of the end of life like me. Without very significant changes and improvements from the House of Lords, we face the all too real prospect of the system provided for by this Bill failing our patients. The complex needs of many of the families I serve require a network of support, not, as the Bill allows, physicians bringing up the possibility of assisted dying to those who are already vulnerable and suicidal.

Leader Live
an hour ago
- Leader Live
NHS should act as ‘engine of local economic growth', Streeting says
It comes as Wes Streeting announced a new pilot scheme which will aim to recruit an extra 1,000 NHS staff from areas worst affected by unemployment. Mr Streeting was in Blackpool on Wednesday to deliver a speech unveiling plans to divert more than £2 billion in NHS spending to working class communities. He also announced changes to the NHS App, with new features that will aim to give patients access to more information and tackle what he described as 'one of the starkest health inequalities'. Speaking of the new programme, Mr Streeting told the PA news agency: 'The pilot we've announced will trial a programme benefiting 1,000 people, including disabled people, people with conditions like autism, carers and people over the age of 50, who, for reasons I cannot understand, are often written off when it comes to being able to go back to work or to get a different job. 'This is the NHS walking the talk. We know that what makes for good health isn't just good treatment, but is a society which creates good health, and that involves employers. 'So this is me and the NHS putting our money where our mouth is, to show that we're going to be good employers providing great opportunities as well as great healthcare.' The pilot will also offer support with job applications and work placements. It comes amid sweeping welfare reforms by the Labour Government which have split the party. In his speech, Mr Streeting said the 'health service should also act as an engine of local economic growth, giving opportunities in training and work to local people'. He told PA: 'The NHS got really important role to play, not just as a provider of public services, but as a provider of great job opportunities. 'I've seen first hand what can happen when the NHS acts as a good local employer and provides opportunities, particularly for people who can often get overlooked and not recognised for their talents.' Mr Streeting also announced that, under reforms included in the Government's upcoming 10-year plan, around £2.2 billion previously set aside to plug financial holes will now be spent on resources in deprived areas. This year, deficit support funding will not go to systems that fail to meet their agreed financial plans and is being phased out entirely from 2026/27, with NHS England chief executive Jim Mackey behind the drive. Struggling NHS trusts will now be required to set out activity and costs in a transparent way. The Government also plans to review GP funding and the GP contract so working-class areas receive their 'fair share' of resources. Mr Streeting told the PA his own experiences of poverty as a child influenced the announcement. 'I'm in politics because I want to make sure that more people from working class backgrounds like mine have the same sorts of choices and chances in life as those from the wealthiest backgrounds,' he said. 'I think the state has a really powerful role to play in making sure that people have those opportunities and security in life. 'But I'm also aware from some of my family's experiences about where the state sometimes lets people down and needs to change and genuinely listen to people and do things with people, rather than to them. 'I don't resent sharp elbowed, middle-class professionals exercising their voice – and I'm obviously one of them now – but we've got to make sure that working class people, people from underprivileged backgrounds, have the same voice, the same choice, the same power and control over their lives as everyone else.' During his speech, Mr Streeting described unequal access to information and choice as 'one of the starkest health inequalities'. To address this, he announced that new features will be introduced on the NHS App as part of the 10 year plan, adding that technology can 'empower patients with choice and control'. A tool known as My Companion will use artificial intelligence to give patients direct access to information. 'It will provide all patients with information about their health condition, if they have one, or their procedure, if they need one,' Mr Streeting added. 'It will get patients answers to questions they forgot to ask or felt too embarrassed to ask in a place that makes appointment. 'So the next time you're at appointment and you're told something doesn't sound right, you'll have at your fingertips the information you need to speak up confidently with the other expert in the room.' Mr Streeting said another feature, known as My Choices, will 'show patients everything from their nearest pharmacy and its opening hours to the best hospital for heart surgery across the country, with patients able to choose based on their preference'.


Sky News
an hour ago
- Sky News
Patient death linked to cyber attack on NHS, hospital trust says
The death of a person has been linked to last year's cyber attack on the NHS. The attack saw 1,100 cancer treatments delayed, 2,000 outpatient appointments cancelled and more than 1,000 operations postponed when cyber criminals attacked two major NHS trusts. Now, the first death of a patient linked to the attack has been confirmed by King's College Hospital NHS Foundation Trust. "One patient sadly died unexpectedly during the cyber attack," said a spokesperson. "The patient safety incident investigation identified a number of contributing factors that led to the patient's death. "This included a long wait for a blood test result due to the cyber attack impacting pathology services at the time. "We have met with the patient's family, and shared the findings of the safety investigation with them." Synnovis, which provides services primarily in southeast London, was the victim of a ransomware attack, understood to be carried out by Russian group Qilin, on 3 June last year. Sensitive data stolen from an NHS provider in a cyber attack was apparently published online. NHS England said a criminal group claimed it has released patient information hacked from Synnovis, which provides pathology services on blood tests. Please refresh the page for the fullest version.