
'GP said my girl had anxiety - real diagnosis is every parent's worst nightmare'
When she took her 'bubbly and active' daughter to the doctor with a pain in her side, mum-of-two Christina Harris knew there was something seriously wrong - but it took multiple trips to get to the bottom of her illness
After complaining about having a sharp pain in her side as well as a fever and breathlessness that came out of nowhere, Christina Harris did what any parent would do and took her daughter to the GP.
However she was not prepared for what was about to come. Doctors told her that her Skye, 10, was suffering from anxiety, but Christina, 46, from Essex, knew that it was unlike her 'bubbly and active' daughter and that there was more to it.
Acting on her mother's instinct, Christina saw that Skye was still in pain, while the fever continued, so she took her to A&E a few days later.
"Sometimes you just have to go with your instincts when you know something is wrong," Christina told The Mirror. Determined to know what was causing her daughter to be in pain, doctors then did several scans, including an X-ray and noticed shadowing on Skye's ribcage.
"They initially thought it may be an infection or something and gave her some antibiotics to clear it up," Christina recalled. "I hoped this was the case, and we went home with antibiotics."
But after a few days, and still unsure, Christina rushed her daughter back to A&E after Skye had another temperature in the middle of the night, and she knew deep down her daughter wasn't getting any better. "You just go into a pilot mode, I was blocking out any type of negative thoughts I was having, and just wanted what was best for my daughter."
During this visit, doctors then found Skye's lungs full of mucus. She was diagnosed with pneumonia, which was the reason for her excruciating pain, and after further investigation and more blood tests, it turned out to be something much worse.
On December 7, 2021, the keen dancer was diagnosed with Acute Lymphoblastic Leukaemia (ALL), a rare type of blood cancer and was blue-lighted to Great Ormond Street Hospital to begin her chemotherapy treatment. "I knew something wasn't right, she kept complaining of this pain, even in her sleep, it wasn't normal," the worried mum reflected.
"It was scary when they told me she had pneumonia. Obviously I did not anticipate what was to come. It's every parent's worst nightmare."
Christina, a mother of two, sadly lost her job as an estate agent because she needed to support her daughter and became a full-time carer. Her son Marley, 13 at the time, was able to spend time at his dad's house more frequently as Christina cared for Skye.
"You just know deep down when something isn't right, but I never thought it would be that Skye had leukaemia, you just have to go with your instincts in these moments and I am so glad I did. When we got the news, I just went into flight mode and I couldn't think of anything other than the fact my daughter had cancer.
READ MORE: 'Entitled mum approached me in restaurant with demanding request for her son'
"I cried so much when we got to Great Ormond Street, but in a strange way, I finally felt safe. I was just so pleased that they had found out what was wrong." Skye then spent 11 days in Great Ormond Street, where she began her chemotherapy treatment.
"We were at Great Ormond Street multiple times a week, as well as appointments at our local hospital too. She was having such aggressive chemotherapy which went on for six months.
"I had to also make sure I was keeping an eye on her temperature, as if it went to 38 degrees I'd need to rush her to hospital. I knew when she wasn't right."
Skye was put on strong antibiotics every time she had a high fever due to her weakened immune system and was having chemotherapy given in multiple ways, including into her thigh, as well as into her spine.
"This type of leukaemia is one of the longest cancer treatments for children and it made Skye really poorly." Skye finished her treatment after a year, and then moved on to maintenance chemotherapy, designed to help keep cancer from coming back after it has disappeared following the initial therapy.
While she felt extremely unwell during her treatment, Skye said she enjoyed going to Great Ormond Street as she had become friends with all of the doctors and nurses. She was also treated to takeaways and feasted on food when she felt up to it.
Skye said: "I wasn't at school and I wasn't making any friends so it was hard, but I got to know all of the nurses and they were really nice to me. It wasn't a nice experience but I managed to find some joys in between and my mum let me have any kind of food I wanted so we would always get a Nando's or a Pizza Express."
Recalling the time spent in hospital, Chrisina said it was "horrendous" and detailed: "It was really hard. You never want this for anyone, let alone your own children and it was really difficult.
"I think you just sort of switch off from everything else and just go into this type of pilot mode. You have to give her everything she needs and I got to a point where I had this diary where I'd tick off hour by hour which medication I was giving her.
"She needed certain medications at exact times so it was a lot to do - I was basically a nurse looking after her. I was trying to just block out any negative thoughts and just focus on giving her what she needed. "The first nine months, when she was having the most intensive part of the treatment, we couldn't leave the house and the only people that could come in were the nurses.
"My parents live in Denmark so I was doing it all alone, and my son Marley had to get dropped at his dad's a lot of the time, especially when Skye needed to be rushed into hospital quickly - even in the middle of the night."
Skye was finally able to ring the bell on March 30 last year and has been in remission since. She also celebrated with an end of treatment party, something she had been looking forward to for the past three years.
Now 13, Skye is doing really well and says she wants to be a nutritionist at GOSH. She said: "I really want to be a nutritionist, my time in treatment has really inspired me to help others like the way the doctors and nurses have helped me.
GOSH Charity is currently raising £300m to build a new Children's Cancer Centre at Great Ormond Street, which will help thousands of children like Skye. Skye and her mum Christina say the new centre will be "amazing" for patients like her.

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Daily Mirror
6 hours ago
- Daily Mirror
'I was being pushed towards heaven and hell - it was a near death experience'
When a tube train failed to stop and crashed into the tunnel at Moorgate, in London killing 43 people and injuring 74 more in 1975 survivor Javier Gonzalez had what he describes as a near death experience For half a century pensioner Javier Gonzalez has believed he is one of the luckiest men alive - after surviving the Moorgate tube crash that killed 43 people and injured 74 others on February 28, 1975. Fifty years ago he sat in the first carriage - which was crushed down from 16 metres long to just 6.1 metres - as it crashed into the wall at 8.46am. It was a miracle he survived and he told The Mirror how he had a near-death experience where he remembers being pushed towards heaven and hell. 'I could see underneath me a valley with a river, trees and people and it felt full of love. I wanted to go there but I also wanted to tell everyone about it,' Javier says, describing the moment when he thinks he had a near death experience. 'The next minute I was being pushed down into a very dark area where I could hear screams, I could smell rotten smells, it was dark and hot. I now know it wasn't what was happening in the tunnel because everyone was either dead or rescued except for me and the two other people, who were trapped who had already passed.' Just after the accident, when people were more sceptical about near death experiences, he says people listened to his story as if he had gone mad. He even heard someone in hospital say, 'poor man, he's gone nuts.' He's since written a book about his experience called A Ticket to Eternity, despite being plagued with medical problems since the accident - including blood clots, a brain tumour and recurring pain in his head. Even neurologists, he says, have not ruled out that his medical issues could be related to the crash. The Moorgate tube crash was the worst peacetime accident on the London Underground, crushing the first carriage, leaving the second folded at the front, as it collided with the first, with the third riding over the rear of the second. Rescuers had to walk over dismembered limbs and dead bodies and a number of people who were decapitated to find survivors. Describing the scene as 'worse than in a horror movie', it took the emergency services 13 hours to remove the injured, many of whom had to be cut free from the wreckage. One rescuer said the front carriage that Javier was sitting in was 'an indescribable tangle of twisted metal' where 'the living and the dead were heaped together, intertwined among themselves and the wreckage.. writhing in agony.' Javier was trapped there for five hours and is now thankful he passed out, as he didn't have to witness the horrific carnage around him. The next thing he remembers was being pulled to safety. 'A man asked if I could move and when I replied that I couldn't, he told me to cover my face as he pulled me out of the wreckage,' he says. 'I was slipping in and out of consciousness and I remember someone injecting something into my hand." What happened next will stay with him for a lifetime. 'I didn't gain full consciousness until the following morning, the Saturday when I woke up in intensive care at St Bartholomew's Hospital with splatters of other people's blood on my clothes, covered in soot and with bits of broken glass in my hair. There was a nurse standing next to me and after asking me how I was feeling she passed me a newspaper. I remember there were images of the accident and my name was on the front page. 'I had amnesia and was confused and I was reading about an accident that was being described as worse than a warzone or a horror movie. Then I just remember feeling really thankful that God had not let me see it.' Javier's hip was fractured into 100 pieces and he had to have a steel rod inserted inside his leg. For the next six months, he relied on crutches to walk, but he considers himself one of the lucky ones. And he was not left traumatised about using the tube, as he knew the chances of anyone having a second accident on the underground like that were extremely unlikely. The near death experience has also left him unafraid of dying. No fault was found with the train after an investigation. The brakes were not applied, and the dead man's handle was still depressed when it crashed. The inquiry by the Department of the Environment concluded that the accident was caused by the actions of Leslie Newson, the 56-year-old driver.


Scottish Sun
7 hours ago
- Scottish Sun
Our ‘fit' dad died weeks after we got his diagnosis – his Apple Watch alerted us & a simple question could've saved him
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Advertisement 9 Lucy with her dad Alan, who could've had longer with them if one simple question was asked by medics, the family believes Credit: Joel Goodman/Pancreatic Cancer UK 9 'Fit and healthy' Alan died four weeks after being diagnosed with pancreatic cancer Credit: Joel Goodman/Pancreatic Cancer UK 9 Alan's children David and Lucy believe their dad could have been saved Credit: Joel Goodman/Pancreatic Cancer UK 'If the doctors had asked about dad's family history, they'd have found out his sister Judy died of pancreatic cancer 12 years before when she was 60,' David, 35, from Preston, Lancashire, tells Sun Health. 'It could have changed everything.' Advertisement Instead, it took 13 months for the retired council project manager to get a cancer diagnosis from the onset of his first symptoms. And when it finally came, it was too late - Alan died just four weeks later, aged 68. Lucy, 33, says: 'The medics never connected the dots despite the fact it felt strange because he was such a healthy person suddenly having issues. 'I find those 'what ifs' really hard to deal with now. 'Had the doctors known about his sister when investigating these sudden health issues in 2023, things may have been so different. Advertisement 'That knowledge, combined with the pre-diabetes and heart issues, should have been three massive red flags. 'We might have had a chance to explore chemo or an operation, or to go private to speed things up. 'Instead, when it did finally get diagnosed, dad's rate of decline was like going from 0 to 100 in no time at all.' I'm a doctor, NEVER ignore these pancreatic cancer symptoms Alan had lived his life by the book, alongside his loving wife Julie, 69, a retired school bursar. 'He was so fit, so healthy,' David says. 'He was cycling 20 to 30 miles four or five days a week. Advertisement 'He'd never had a day off work in his life.' In May 2023, during a regular cycle with his club, Alan felt faint. His Apple Watch showed an erratic heartbeat and Julie rushed him to A&E. Doctors discovered Alan was dehydrated and suffering from atrial fibrillation - an irregular heart rhythm. By August, blood tests flagged pre-diabetes. He was told to start taking up to 10 tablets a day. Advertisement Beauty business owner Lucy, also from Preston, says: 'He was absolutely mortified. 'He was a really proud man who, like mum, took good care of himself but he actually got quite tearful because the doctor suggested he may be eating the wrong things.' 9 Alan's Apple Watch showed an erratic heartbeat and wife Julie rushed him to A&E Credit: Joel Goodman/Pancreatic Cancer UK 9 If the doctors had asked about Dad's family history, they'd have found out his sister Judy died of pancreatic cancer 12 years before, David tells Sun Health Credit: Joel Goodman/Pancreatic Cancer UK Alan carried on taking holidays in his beloved motor home with Julie and trying to stay active. Advertisement He became increasingly conscious of what he was eating. On May, 26, 2024, Alan saw a cardiologist for the irregular heartbeat, atrial fibrillations, that were still bothering him. His heart issues remained, and he was told he'd likely need cardioversion to shock his heart back into rhythm. But the very next day, on the May Bank Holiday, he took a turn for the worse. TURN FOR THE WORSE Lucy says: 'I looked at dad that day and I just cried. He looked grey. He'd lost weight. Advertisement 'We had walked into the village that day to watch my nephew [David's son] in a parade, and I ended up having to link arms with dad and he was propping himself up on a wall as he was tired and had a pain in his upper stomach. 'I was such a daddy's girl, I became obsessive from that day on. 'I think because we were so close, I just knew he had cancer and I was terrified.' Alan returned to the GP on May 31, following the sudden decline in his health. That week, he had numerous doctor's appointments. Advertisement He was told he now had type 1 diabetes and started having to inject insulin. But alarm bells rang when blood tests showed abnormalities in his liver and pancreas. 9 Alan with his grandson George Credit: Joel Goodman/Pancreatic Cancer UK 9 Alan's wife Julie Credit: Joel Goodman/Pancreatic Cancer UK 'The GP said he suspected pancreatic cancer and was referring Dad on the two-week cancer pathway,' says David. Advertisement 'I had taken that day off and, when I heard, I Googled it on the beach while my son played. It was terrifying. 'It said he could have months - maybe a year at best so from that day on, until after he died, I chose not to look again because I wanted to remain positive and hopeful for Dad.' A day later, Alan began to notice his vision worsening. He was rushed to Lancaster Hospital by ambulance. His insulin was increased which helped with his sudden diabetes diagnosis, but over the next week, he found it increasingly hard to eat without experiencing huge discomfort. Advertisement Lucy, who had moved back into the family home, admits: 'I was obsessive, thinking I could heal him with juices. 'One of my friends made some for us and I bought a juicer. 'I'd buy all organic vegetables and fruit and leave several options for him next to a little note that said 'I love you'.' The gastro consultant confirmed pancreatic cancer and that it had spread to his liver but it was all very fast. David Alan's weight loss, pain and weakness continued. On June 10, a full-body CT scan was carried out. Advertisement A week later, a doctor called Alan to say he had looked at the scan results and found blood clots on Alan's lungs and he needed to make his way to the hospital urgently. What you need to know about pancreatic cancer AS with most cancers, the earlier you detect pancreatic cancer the better a patient's chance of survival. That's why it's so important to know the signs and symptoms, and to act and seek your GP if you're worried. Here, Nicci Murphy, a specialist nurse who staffs Pancreatic Cancer UK's Support Line, reveals what you need to know. How common is pancreatic cancer? Around 10,700 people are diagnosed with pancreatic cancer each year in the UK. Are there different types? There are different types of pancreatic cancer, the most common being pancreatic ductal adenocarcinoma, which accounts for around 95 per cent of cases. However, there are other, less common types of pancreatic cancer, such as pancreatic neuroendocrine tumours (PNETs). What are the early warning signs and symptoms you should look out for? Pancreatic cancer often doesn't cause symptoms in the early stages which makes it incredibly difficult to detect. As the cancer grows, it may start to cause symptoms, but they are often vague and associated with common, less serious conditions. Common symptoms of pancreatic cancer include: tummy (abdominal) and/or back pain unexplained weight loss and indigestion. Other symptoms include: loss of appetite changes to bowel habits – including steatorrhoea (pale, smelly poo that may float), diarrhoea (loose watery poo) or constipation (problems emptying your bowels) jaundice (yellow skin and eyes, dark urine, pale-coloured stools and itchy skin) recently diagnosed diabetes or sudden, uncontrolled blood sugars in diabetics problems digesting food – such as feeling full quickly when eating, bloating, burping or lots of wind feeling and being sick (nausea and vomiting) and difficulty swallowing. If a person has any of these symptoms and they don't know why they have them, they should contact their GP or call NHS 111. If they have jaundice, they need to go to their GP or A&E straight away. What's the treatment and survival rate? Pancreatic cancer is the deadliest common cancer: more than half of people die within three months of diagnosis. Research into the disease has been underfunded for decades, resulting in survival rates that have barely improved in the last 50 years – in stark contrast to other cancers. Due to the vague symptoms associated with the disease and a lack of early detection test, 80 per cent of people aren't diagnosed until after the cancer has spread, meaning they are unable to have lifesaving treatment. Surgery is the only potentially curative treatment for pancreatic cancer yet just 10 per cent of people are eligible for it. It was that day, on June 17, 2024 that he finally got a diagnosis. 'The gastro consultant confirmed pancreatic cancer and that it had spread to his liver but it was all very fast,' David says. 'They booked a biopsy for June 27, but Dad was already deteriorating rapidly.' Lucy, who was waiting with David in her car outside the hospital, recalls: 'I was beside myself when I saw them both. Advertisement 'They were walking slowly towards the car clearly distressed and Mum said, 'it's not good.' 'They could barely speak because of the emotion of it all and then dad just gave me a massive hug and we were all just crying. It's something I'll never, ever get over.' Alan grew sicker by the day. He suffered violent hiccups, caused by the tumour blocking his duodenum - part of the small intestine. His first oncology appointment was set for July 9. 'It felt like everything was too slow,' David says. Advertisement 'Every day matters with this type of cancer. It's one of the most aggressive out there. We kept being told there were processes to follow. But it felt like no one was in a rush.' Alan suddenly took a serious turn. 9 Alan suffered violent hiccups, caused by the tumour blocking his duodenum - part of the small intestine Credit: Joel Goodman/Pancreatic Cancer UK 9 You can't turn a blind eye to any symptoms, says Lucy Credit: Joel Goodman/Pancreatic Cancer UK Because he was so dehydrated, medics gave him an IV drip, not realising at this point his tumour had caused a blockage. Advertisement When Alan returned home, he started being violently sick because of all the fluids he'd been given, and his hiccups were so severe, Lucy says, 'it was like he was fitting'. After returning to hospital, on July 15, in agonising pain doctors fitted a stent to unblock his duodenum, in the hope that if it was successful he could begin chemotherapy. The next day, it was the Euro Cup final which will forever remain a bittersweet memory for David. David says: 'England were playing Spain, and I watched it with Dad in hospital but it was a very surreal experience for me because I was driving through my town watching people going to the pub to watch it but I was going to hospital to watch it with my dad, who was dying.' The stent operation appeared to go well. Advertisement 'He came out of theatre with a smile and a thumbs up and said, 'I'm ready for the chemo now,'' David remembers. But just like his sister Judy, Alan deteriorated within days. Lucy says: 'The last few hours, when dad was in hospital, were just awful because he was in so much pain he couldn't even speak. 'I was just holding his hand and saying 'Dad, just picture yourself on your bike, and you're going to get a massive 99 ice-cream' because that's what he loved.' FINAL HOURS Finally, after the help from his sister-in-law, Alan was taken to the hospice to see out his final hours in peace with Julie, David and Lucy by his side. Advertisement He died in the early hours of July 18, just nine hours after arriving at the hospice. 'It was peaceful. The hospice staff were incredible,' David says. 'Absolutely nothing can prepare you for the loss of a parent,' Lucy says. 'Every day you wake up and it hits you, like, 'oh my gosh, did that actually happen?'.' David, who runs a cheese export business, says doctors need better training to ask about simple risk factors. Advertisement 'A year earlier, if they'd looked at Dad's family history, if they'd joined the dots - it could've been a totally different outcome,' he says. The siblings are now backing calls for more investment in early detection, including a breath test in development, that could flag pancreatic cancer in its early, silent stages. Absolutely nothing can prepare you for the loss of a parent. Lucy 'If you catch it early, there are more options - like being able to operate, chemotherapy, and survival rates change dramatically,' David says. 'But once it's late, it's too aggressive. Dad never stood a chance. 'We were told things had changed since Auntie Judy died. But with pancreatic cancer, nothing has changed.' Advertisement 'You can't turn a blind eye to any symptoms,' Lucy adds. 'Detecting pancreatic cancer is so difficult and there's just not enough awareness about it. 'We're coming up to the first of everything. I know the first anniversary will be difficult. 'But I will always remember dad as the most incredible, caring person who was so much fun. 'We were so lucky to have him.'


Daily Mirror
14 hours ago
- Daily Mirror
Everything you should do if you believe someone is missing
Having a loved one go missing is difficult to deal with so having clear idea of what steps to take is important. Guidance from police and the charity Missing People helps Someone is reported missing every 90 seconds in the UK, which is more than 170,000 people a year. Of these, about 75,000 are children, and nearly 96,000 are adults. When a loved one goes missing, it can be difficult to know what to do. Earlier this year, The Mirror teamed up with the charity Missing People to launch the Missed campaign, raising awareness of every publicly-listed missing person in the UK. The police and Missing People provide advice on how to cope when someone you know goes missing, as well as what steps need to be taken - and we've used this to put together a simple guide outlining each important part of the process, from making the report to searching for your loved one. How can you report a missing person? If someone goes missing, you should contact anyone you think may know their whereabouts, and if you're still concerned, contact your local police. It is a common misconception that you have to wait 24 hours before contacting the police. If you are concerned, report it straight away. The police may ask you for a photo of the missing person, details of their friends and relatives, places they often visit, whether they have a medical condition, and for a sample of their DNA (such as from a toothbrush). The person will be recorded as missing and their details made available to other UK police forces within 48 hours. If someone goes missing abroad, you should contact your local police, who will then contact the force in the relevant country through Interpol, as well as the Foreign, Commonwealth and Development Office. You can do this by calling 020 7008 5000 and asking for 'Consular Assistance'. DEMAND ACTION FOR MISSING PEOPLE Too many missing people are falling through the cracks - harmed while away, and ignored when they return. We need a proper government strategy led by the Home Office, Education, and Health departments to stop this crisis. Right now, there's no real support. People go missing again and again - yet no one's asking why. We're calling for: A new national strategy for missing children and adults Proper support for missing people when they return Investment to stop people going missing in the first place At 10,000 signatures, the government has to respond. At 100,000, it will be debated in Parliament. That's our goal - real action. What will the police do during a missing person case? The police will sometimes allocate a Family Liaison Officer (FLO) to a missing person case, who will act as a consistent point of contact for the family, and provide support and information about the investigation. After 72 hours, the police working on the case have to tell the UK Missing Persons Unit, which is part of the National Crime Agency. The unit carries out enquiries on behalf of local forces, keeps a database of missing and found people, and manages the forensic database of DNA profiles and fingerprints. The police will also have to decide if a case is high risk, medium risk, low risk, or no apparent risk, after a person is reported missing. They will take into account factors like age and health - but the risk level can change during the investigation if new information comes to light or circumstances change. How can you find a missing person? As well as reporting the missing person to the police, you can call the person, search the places where you think they could be, and speak to people that may know where they are, the Missing People charity explained. You could try ringing around hospitals to see if they have had any recent unidentified individuals admitted. You should ask family and friends to help you as this can 'speed things up and make you feel more supported and less alone'. It is also a good idea to make a note of all the things you have done, places you have searched, and the people you have spoken to, as this may be helpful later. If the person is still missing after several weeks, you should make sure to know who your point of contact is in the police and what is happening in the search. You should also think about publicity and can share posts on social media to raise awareness. Missing People said: 'When sharing our appeal, if you feel comfortable to do so, you could try targeting useful agencies such as local newspapers and asking them to share it.' You could also reach out to your loved one's favourite sports team, if they have one, to ask them to help share the appeal. If Missing People has launched a public posted campaign for your loved one, you will receive a copy via email. You can hand this out to places like pubs, nature reserves, and cafes, as well as other places where they have lots of connections such as a town they used to live in. Talking to family and friends about how you're feeling, or seeking professional support, is a good idea if they remain missing after several months. There are many ways to keep the media interested in your appeal after a long time, such as by making a page or group on social media, launching Facebook fundraisers, and getting in touch with media outlets as you reach notable timelines. Missing People advised: 'If you have any photographs of your loved one which you have not yet shared publicly, consider if you would like to share them online and with the media. Sometimes having a new photograph, or even an alternative such as them with a beard or without, can help to create more interest in the appeal. It can also jog peoples' memories.' It may be worth considering whether Age Progression would be useful if your loved one has been missing a long time. This method involves changing a photo of the person to show how they would look after aging or maturing. The police warn against putting yourself in danger while searching for your loved one. It says: 'Let police deal with any specialist searches in places like mountains or water.' However, there are things you can do to help with the search, which includes leaving the missing person's bedroom and things alone, and not touching their hairbrush or toothbrush, as this could be used to collect a DNA sample. When is a missing person case closed? A missing person case is only closed when the person is found. However, when it has been 12 months, the investigation will be reviewed to consider if it can become a 'Long Term Missing' case. During the process, there will likely be several reviews held by the police. Guidance states that reviews should be completed at the latest after 28 days, three months, six months, and 12 months, then annually thereafter. It explains: 'If significant information comes to light, this should trigger an immediate review. Consideration may also be given to cold case reviews of outstanding missing person cases.' Families should be 'given reasonable expectations about ongoing contact during long-term cases' and be told about the review process and updated on the outcomes. Missing People said: 'If you do not feel like these expectations are being followed by your police force you should ask to speak to the responsible officer and explain your concerns. If you still feel that they are not communicating reasonably regularly you can consider making a complaint.'