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Tear-jerking moment brave cancer survivor surprises heroic donor who saved her life

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Tear-jerking moment brave cancer survivor surprises heroic donor who saved her life

WATCH the moment a blood cancer survivor met the young stranger who provided the stem cell donation that saved her life.

Alison Belsham, from Newport in South Wales, held back tears as she approached her donor, 31-year-old Rachel Rees, and invited her in for a hug.

Alison Belsham and donor Rachel Rees meet for the first time at surprise get-together

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Alison Belsham and donor Rachel Rees meet for the first time at surprise get-togetherCredit: SWNS
Alison held back tears as she approached Rachel

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Alison held back tears as she approached RachelCredit: SWNS

“There can never be enough thank yous,” the 57-year-old told her.

Alison was diagnosed with leukaemia for the second time in 2017, prompting a worldwide search to find a bone marrow donor.

”The news was absolutely devastating for me and my family as the future, once again, became uncertain,” she said.

Her doctor said a donor stem cell transplant was the “last hope” of saving her life.

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Despite over 40million stem cell volunteers across the world, three in ten patients will not find a suitably matched donor.

Medics eventually found a match on the other side of the world in Australia, where Rachel, originally from Llanelli, also in South Wales, was living at the time.

Now, a video revealing the pair’s emotional meeting has been published online and is sure to trigger goosebumps.

The clip shows Alison expressing her appreciation to Rachel, as she said: “I now get the chance to live a full life, spend precious time with my children and see my grandson grow up.”

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Rachel had flown home from Australia expecting to visit friends and loved ones in her hometown.

The most common symptoms of pancreatic cancer – as patients share their stories

But unbeknown to her, her family and stem cell recipient arranged a surprise get-together for the pair to meet.

The transplant Alison received used Rachel’s healthy donor stem cells to replace her own cancer-causing cells.

She has since been cancer-free. 

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The women are hoping their story will encourage more people to sign up to the register and help in the fight against blood cancer.

 “My initial treatment involved five rounds of chemotherapy, which appeared to be successful,” Ms Belsham said, speaking of her illness.

“After a year and a half in remission, however, I had a phone call to say that my cancer had returned.”

The women are hoping their story will encourage more people to sign up to the register

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The women are hoping their story will encourage more people to sign up to the registerCredit: SWNS
Rachel and Alison with their family members

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Rachel and Alison with their family membersCredit: SWNS

Around a quarter of a million people are living with blood cancer in the UK, with over 40,000 being diagnosed every year. 

While some can be successfully treated with chemotherapy and surgery, for other patients, this treatment can wreck the body’s ability to make new and healthy blood cells.

How do I donate?

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Every 14 minutes someone in the UK is diagnosed with a blood cancer.

A stem cell transplant from a stranger can be their only hope. 

To become a donor, you need to join the stem cell register.

Complete the online form to request a swab pack. This will be posted to you, you complete it and post it back.

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It could take years before you are identified as a ‘match’ with a patient. And you may never be called on at all. 

If you are, you must undergo a thorough examination to make sure there are no medical reasons you cannot donate.

There are two types of donation:

  1. Blood stem cell donation: The most common process is where you receive injections for four days to boost your stem cells. On the fifth day, you are connected to a machine which collects the extra stem cells, it’s sort of like giving blood.
  2. Bone marrow donation: Stem cells are removed from your hip bones while under a general anaesthetic in the hospital.

It is important to point out that no medical procedure is risk free, but experts say 16 or 17-year-old donors are at no more risk than an adult.

In these cases, patients will need a stem cell transplant – special cells produced by the bone marrow that can turn into different types of cells.

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“I am so proud of her, proud of her recovery, proud of her tenacity and I am just so thankful that she reached out to meet me,” Rachel said.

“I am so glad to see Alison happy and healthy, having our families meet has been so, so special.”

Help people in their ‘greatest time of need’

Christopher Harvey, head of the Welsh Bone Marrow Donor Registry, said: “Blood cancer patients around the world face a daily, and increasingly urgent, search for a suitable stem cell match.

“The requirements for matching a patient with a donor are very specific, but the opportunity to find a life-saving match increases as more volunteers sign up.

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“If you’re 16-30 from a caucasian background or 16-45 from a black, Asian, mixed race or minority ethnic background, you could be the one person in the world who could be the match.

“That’s why we are urging more people to sign up to our Registry and help people like Alison in their greatest time of need.”

Leukaemia: Everything you need to know

LEUKAEMIA is a type of blood cancer that affects cells in bone marrow and attacks the immune system.

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There are several types of leukaemia but what are the symptoms and is it treatable?

What causes leukaemia?

In most cases of leukaemia, there is no obvious cause.

It is a cancer that leads to the body making too many abnormal white blood cells which means the body is less likely to be able to defend itself against infection.

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These blood cells are not fully developed and are called leukaemia cells.

The disease is often classified as the type of cell affected (myeloid or lymphatic) and how it progresses (acute or chronic).

What are the symptoms of leukaemia?

There are no specific signs or symptoms which would allow a doctor to make a diagnosis without lab tests.

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In all types of leukaemia, symptoms are more commonly caused by a lack of normal blood cells than by the presence of abnormal white cells.

As the bone marrow becomes full of leukaemia cells, it is unable to produce the large numbers of normal blood cells which the body needs.

This can lead to:

  • Anaemia
  • Weakness and tiredness
  • More frequent infections
  • Fever
  • Bleeding and bruising

What are the different types of leukaemia?

There are four main types of leukaemia.

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They are:

Acute Lymphocytic Leukaemia (ALL) – A rapidly progressing form of the disease. More common in children.

Acute Myeloid Leukaemia (AML) – Rapidly progressive. More common in adults.

Chronic Lymphocytic Leukaemia (CLL) – Slowly progressing form and more common in adults.

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Chronic Myeloid Leukaemia (CML) – Progresses slowly and is more common in adults.

Can leukaemia be treated?

Currently, there are five ways leukaemia can be treated.

They are:

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Chemotherapy: These are cell-killing drugs which kill and/or stop them from dividing. Chemotherapy is often given in blocks or cycles of treatment. One cycle of treatment will consist of a series of doses of chemotherapy followed by a break for the healthy cells to recover.

Radiation therapy: This treatment uses high-energy radiation to kill cancer cells. It is not used to treat all types of leukaemia.

Targeted therapy: Drugs which specifically recognise and kill leukaemia cells.

Biological therapy: A treatment which uses the immune system to destroy leukaemia cells.

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Stem cell transplant: Younger patients may be given a stem cell transplant (bone marrow transplant). This may be done using your own healthy stem cells or stem cells from a donor. This is most commonly done for acute leukaemia if chemotherapy does not cure the disease.

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Horrifying reality of ‘rogue’ funeral directors laid bare at inquiry into NHS morgue monster who raped corpses

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Horrifying reality of 'rogue' funeral directors laid bare at inquiry into NHS morgue monster who raped corpses

FUNERAL directors must be regulated to stop rogue operators, warn experts investigating the NHS morgue monster David Fuller.

Fuller was sentenced to life in prison for murdering two women and sexually abusing the bodies of more than 100 at hospitals in Kent.

David Fuller was jailed for murder and sexually abusing dead women's bodies at the hospital where he worked

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David Fuller was jailed for murder and sexually abusing dead women’s bodies at the hospital where he workedCredit: PA
The Fuller Inquiry warned current rules mean anyone can set up a funeral home (stock image)

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The Fuller Inquiry warned current rules mean anyone can set up a funeral home (stock image)Credit: Alamy

Sir Jonathan Michael, chair of the inquiry into his crimes, said the funeral industry needs urgent reform.

He said he has sped up his work due to “recent distressing reports”.

Three people were arrested in the summer in connection with a funeral home in Hull, East Yorks, after families found loved ones’ remains had been mixed up or lost.

Past incidents have seen bodies treated inappropriately or left to rot in funeral parlours.

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Read more on David Fuller

NHS hospital mortuaries have also been found to be too small, too warm or not properly secured.

Anyone can set themselves up as a funeral director and keep the bodies in their garage without anybody being able to stop them. That cannot be right

Sir Jonathan Michael Chair of the Fuller Inquiry

The Fuller inquiry found funeral directors do not need a licence, qualifications or training, and described the sector as an “unregulated free-for-all”.

Sir Jonathan said: “It is clear to me that many people believe or assume that the sector is already regulated, and they are shocked to find this is not the case. 

“The fact is that anyone can set themselves up as a funeral director. 

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“They could do it from their home and keep the bodies of the deceased in their garage without anybody being able to stop them. 

“That cannot be right.

“My hope is that publishing this interim report now will assist both the Government and the funeral sector itself to take steps that assure the public that care in the funeral sector is fit for purpose. 

“We need a regulatory regime that will not tolerate any form of abuse or any practices that compromise the security and dignity of the deceased.”

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Health Secretary Wes Streeting said: “The Government is committed to preventing any similar atrocities happening again and ensuring
that the deceased are safeguarded and treated with dignity.”

FULLER ‘FREE TO OFFEND’ DUE TO HOSPITAL FAILINGS

MORGUE monster David Fuller was free to assault dead women for 15 years due to “serious failings” at the hospitals where he worked, a report found.

The double killer abused at least 101 women while working at mortuaries in Tunbridge Wells Hospital and at the former Kent and Sussex Hospital.

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A probe found there were “missed opportunities” to stop the necrophiliac’s 15-year rampage.

His youngest victim was a nine-year-old girl and the oldest was 100 years old, with Fuller sometimes violating the bodies more than once.

Inquiry chairman Sir Jonathan Michael said: “Failures of management, of governance, of regulation, failure to follow standard policies and procedures, together with a persistent lack of curiosity, all contributed to the creation of the environment in which he was able to offend, and to do so for 15 years without ever being suspected or caught.

“Over the years, there were missed opportunities to question Fuller’s working practices.

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“Had his colleagues, managers and senior leaders been more curious, it is likely that he would have had less opportunity to offend.”

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Women are having their pain dismissed more than men at almost EVERY stage of their lives, research reveals

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Women are having their pain dismissed more than men at almost EVERY stage of their lives, research reveals

WOMEN are having their pain dismissed more than men at almost every stage of their lives, according to research.

A study of 5,000 adults examined how everyday pain is poorly understood and mistreated, with 81 per cent of 18-24-year-old women feeling their pain is ignored or dismissed.

The majority of young women feel their pain is ignored or dismissed

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The majority of young women feel their pain is ignored or dismissedCredit: Getty – Contributor

This compares to just 73 per cent of men of the same age.

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While more than half of women aged 45 and over feel they have been ignored or dismissed, this drops to 49 per cent of men.

In addition, four in 10 women with menopause-related pain had it dismissed or ignored, and one in six women over 45 claimed it took longer than a year for the cause of their suffering to be diagnosed.

Overall, 19 per cent of all women felt their pain was dismissed by healthcare professionals for more than five years compared to 16 per cent of men.

Read more on women’s health

As a result, one in five said their career has been impacted because of their pain.

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The research was commissioned by Nurofen and its parent company Reckitt, as part of its latest Gender Pain Gap Index Report, which has been tracked annually since 2022.

Gabby Menezes-Forsyth, 25, suffered extreme period pain as a teenager before an endometriosis diagnosis.

She said: “I felt from an early age that the extreme period pain I was experiencing seemed to be worse than others, but I didn’t have a frame of reference for what was normal.

“I felt dismissed as ‘dramatic’ by everyone – from loved ones to teachers. In frequent trips to the GP, their dismissal never appeared cruel or to suggest that I wasn’t in pain, but rather that there was nothing they could do.

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“Ultimately, it was only after suffering a miscarriage at age 22 that I was diagnosed with a biconcave uterus and endometriosis.

“Even with the clarity that the diagnosis offered, it was a difficult realisation to come to, understanding that this would always be something that would impact my life.”

The research shows that the average Gap stands at seven per cent, indicating that more women than men have had their pain ignored or dismissed.

While this year’s Gap has narrowed (two per cent in 2024 vs 11 per cent in 2023), a higher number of women felt their pain was ignored or dismissed (62 per cent in 2024, 49 per cent in 2023 and 56 per cent in 2022.

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A third of women felt it has impacted their mental health – up from a quarter in the 2023 report.

And one in four even started to question their own sanity, believing their pain wasn’t real after having it dismissed.

Clare Knox, founder and CEO of See Her Thrive, said: “So much is talked about the Gender Pay Gap – a similar issue, which needs fixing.

“But this report shows the Gender Pain Gap is also holding so many women back from reaching their true potential and climbing the career ladder.

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“We need to start supporting women to thrive in every aspect of their lives, whether that’s helping them manage pain so they can carve out the career they want, or working with organisations to create environments which empower women’s health in the workplace.”

It also emerged the workplace was found to be one of the most common places for pain to have been overlooked for 40 per cent of women.

And only a fifth are comfortable talking about their pain to HR or their manager in the workplace.

But the dismissal by a health care professional is happening as young as between 10 and 15 for one in 10 girls.

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Dr Bill Laughey, senior medical scientist at Reckitt, which has also announced a partnership with Plan International UK to support girls’ health literacy, said: “With three years of data, we can now start to see the nuances of how women’s pain is dismissed and, crucially, use this insight to help address gender biases for those who experience it the most. 

“This complements our wider commitments to our research programmes, working with Imperial Consultants, London to identify what education the next generation of HCPs want to see while supporting the Royal College of GPs in providing training around gender bias in primary care settings.”

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35 MIN Full Body Workout: Vier Runden Intervalltraining mit Kaya Renz 💥 | ohne Geräte

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35 MIN Full Body Workout: Vier Runden Intervalltraining mit Kaya Renz 💥  | ohne Geräte



Hier kommt ein Full Body Workout, das es in sich hat! Zusammen mit Fitness-Coach Kaya kannst du in 35 Minuten deinen ganzen Körper trainieren und deinen Puls ordentlich nach oben treiben.

Dich erwarten vier Runden Intervalltraining, ein Tabata und eine kleine, schweißtreibende Überraschung am Schluss. Bist du bereit? Auf geht’s!

Hier findest du mehr Videos von Kaya Renz:

YouTube: https://www.youtube.com/channel/UCN_hKvlq5WuakrFDoOA-Ipw *
Instagram: https://www.instagram.com/kaya_renz/ *
Web: https://www.kayarenz.de/ *

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Für dieses Training brauchst du keine Geräte, eine Matte und dein eigenes Körpergewicht reichen vollkommen aus. Viel Spaß!

Du willst noch mehr trainieren? Hier sind noch ein paar Vorschläge für dich:

16 MIN Workout: Oberkörper-Training mit Kaya Renz | ohne Geräte 💥

17 MIN Faszientraining: Das Blackroll-Workout gegen Muskelkater | mit Kaya Renz 🧘‍♀️

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4 MIN Tabata: Intensives Ganzkörper-Workout mit Kaya Renz 🧭 | mit Miniband

00:00 Intro
00:29 Warm-up
07:27 Zirkel Nr. 1
12:20 Zirkel Nr. 2
16:57 Zirkel Nr. 3
21:49 Zirkel Nr. 4
26:19 Tabata
30:49 kleine Überraschung
32:00 Cool Down
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Mass rollout of fat jabs to unemployed will ‘overwhelm’ the NHS – as clinics already struggle with demand

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Mass rollout of fat jabs to unemployed will ‘overwhelm’ the NHS - as clinics already struggle with demand

Weight loss jabs are a hot media topic at the moment, with hundreds of success stories from people who shed the pounds.

In March 2023, the NHS announced it would make Wegovy, a drug made by Danish firm Novo Nordisk, available on prescription to thousands of obese Brits.

It contains the drug semaglutide, which is said to have helped reality star Kim Kardashian and Twitter boss Elon Musk lose weight.

Wegovy, which helped a third of people reduce their weight by 20 per cent in trials, is now available from pharmacies like Boots.

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How do they work?

The jabs work by suppressing your appetite, making you eat less and therefore lose weight.

To do this, semaglutide mimics the role of a natural hormone, called GLP-1.

GLP-1 is part of the signalling pathway that tells your body you have eaten, and prepares it to use the energy that comes from your food.

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London GP and founder of wellgoodwellbeing.com, Dr Zoe Watson, said: “Your body naturally produces an appetite regulating hormone called glucagon-like peptide-1.

“These jabs work by regulating your appetite, which can lead to eating fewer calories and losing weight.”

Aren’t they diabetes drugs?

Semaglutide, the active drug in Wegovy, was originally sold under the name Ozempic specifically for diabetes patients.

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But people started noticing it helped suppress their appetites, stopping them eating as much and helping them shed the pounds.

Novo Nordisk then developed Wegovy, which contains the same chemical but at higher doses specifically to aid weight loss.

Wegovy is not prescribed for diabetes patients.

Can I get them?

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Wegovy is offered on prescription to obese adults given specialist weight loss treatment.

The NHS currently also offers a similar drug called Saxenda, or liraglutide.

Both are only available throught specialist weight management services, which means you have to be referred to clinics led by experts.

GPs can’t prescribe them on their own, Dr Watson said. 

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The jabs have to be taken as part of an overall programme to help with lifestyle changes and psychological support to get the best effect from the medication prescribed. 

Are there any risks?

Like all medicines, the jabs do not come without side effects.

Around half of people taking the drug experience gut issues, including sickness, bloating, acid reflux, constipation and diarrhoea.

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Dr Sarah Jarvis, GP and clinical consultant at patient.info, said: “One of the more uncommon side effects is severe acute pancreatitis, which is extremely painful and happens to one in 500 people.”

Other uncommon side effects include altered taste, kidney problems, allergic reactions, gallbladder problems and hypoglycemia.

What other options are there?

Mounjaro (brand name for tirzepatide) also came onto the market in early 2024.

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Like Wegovy, tirzepatide stems from a drug originally designed to treat diabetes.

The weekly injection helped overweight people drop more than two stone in 18 months.

It is available with to order with a prescription online from pharmacies including Superdrug and LloydsPharmacy Online Doctor.

It works in a similar way to Wegovy and Saxenda, but is more effective.

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Dr Mitra Dutt from LloydsPharmacy says: “Based on clinical trials, 96 per cent of people were able to lose more than five per cent of their body fat using Mounjaro. In similar trials, 84 per cent of people lost more than five per cent of their body weight on Wegovy, and 60 per cent on Saxenda.

“Mounjaro works by activating two hormonal receptors (GIP and GLP-1), which enhance insulin production, improve insulin sensitivity, and work to decrease food intake.”

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WORKOUT FOR PREGNANT WOMEN

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WORKOUT FOR PREGNANT WOMEN

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Bake Off star slammed for ‘trivialising’ serious health condition with ‘offensive’ comments

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Bake Off star slammed for 'trivialising' serious health condition with ‘offensive’ comments

GREAT British Bake Off star Ravneet Gill has issued an apology after making “harmful” comments on spinoff show An Extra Slice.

The chef and author, 33, appeared on the Channel 4 programme alongside host Jo Brand and guests Jonathan Ross and Josh Pugh on October 10.

Ravneet Gill 'made light' of coeliac disease on The Great British Bake Off: An Extra Slice

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Ravneet Gill ‘made light’ of coeliac disease on The Great British Bake Off: An Extra SliceCredit: Channel 4 / The Great British Bake Off: An Extra Slice
She has since apologised for her 'harmful' comments

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She has since apologised for her ‘harmful’ commentsCredit: Instagram / @ravneeteats

While discussing the Bread Week challenges, Gill told the panel: “Well, I love bread, but my mum’s coeliac so she shouldn’t eat bread, but she still loves it, she still eats it.”

Her remarks were criticised by the Coeliac UK, and hundreds of viewers with the autoimmune condition, which requires a strict gluten free diet and affects one in 100 people.

In an open letter to the Bake Off producers, charity CEO Hilary Croft said Gill had “trivialised” coeliac disease, which can lead to severe pain, recurrent miscarriage and even bowel cancer if not properly managed, and “sent a harmful message to the public”.

In response, the Junior Bake Off judge said on Instagram: “I want to make it really clear that my intention was not in any way to cause any misinformation about the severity of coeliac disease or to downplay it at all.

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READ MORE ON COELIAC DISEASE

“For that, I hold my hands up and that was really never my intention.”

She added: “For those of you that don’t know me, I thought I’d provide a bit of context to my work and what I do.

“When I was in my 20s, I worked in London’s first gluten-free restaurant, long before platforms like YouTube and Instagram were as big, and I spent a lot of time educating myself.

“I also have spent the last year writing a lot more gluten free recipes for the community, and that’s because I get asked about them a lot.

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“I just want to circle back and let you know that I didn’t intend for those comments to cause harm, and the fact that they did really upset me, and I’m sorry about that.”

She insisted that her mum isn’t upset, and that “in a fast-moving panel show, sometimes it’s hard and you can’t get your words out, and I should have provided more context”.

Coeliac Disease suffers tell how it effects them and how it is different for everyone

Brand saw the funny side, saying of Gill’s mum: “Good for her.”

“And good for whoever cleans up after her,” Ross joked, followed by laughter from the studio audience.

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Croft “expressed concern” over the interaction, as did several influencers and hundreds of social media users.

One person wrote on X, formerly Twitter: “Her comments were ridiculous.

“Eating gluten when you have coeliac disease is extremely damaging and you should not be encouraging this.”

While another said: “It was unbelievable. Ravneet is a Junior Bake Off judge!

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“I can’t believe how ill-informed she is and how coeliac disease was trivialised.”

And gluten free blogger Becky Excell said: “This is so frustrating when we are all working so hard to raise awareness of coeliac disease in the right ways, and especially with it not being too far from the festive season when we really need everyone to understand more than ever.

“It’s especially frustrating when a programme isn’t even live as itcould have been stopped from being aired.

“Following a gluten free diet isn’t for fun or enjoyment, it’s not a choice.”

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Gill appeared on the show with Jo Brand, Josh Pugh and Jonathan Ross

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Gill appeared on the show with Jo Brand, Josh Pugh and Jonathan RossCredit: Channel 4 / The Great British Bake Off: An Extra Slice
Gill's mum has coeliac disease

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Gill’s mum has coeliac diseaseCredit: Instagram / @ravneeteats
Jonathan Ross also made jokes about the condition

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Jonathan Ross also made jokes about the conditionCredit: Channel 4 / The Great British Bake Off: An Extra Slice

In a public letter to the producers of An Extra Slice, Croft said: “We are writing to you as Coeliac UK, the national charity representing the interests of people living with coeliac disease.

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“We would like to express our concern regarding the comments made by Ravneet Gill during the latest episode of An Extra Slice (series 15, episode 3), which aired on October 10 at 8pm.

“During the show, Gill made light of coeliac disease when discussing her mother’s condition.

“The comments [made by Gill, Brand and Ross] trivialise coeliac disease and send a harmful message to the public.

“Coeliac disease is a serious autoimmune condition where the ingestion of gluten triggers an immune response that damages the gut lining, leading to nutrient malabsorption and a host of potential health complications.

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“Even the smallest crumb of gluten can cause severe symptoms, including debilitating pain, prolonged suffering and even recurrent miscarriage, as well as long-term health risks such as osteoporosis and, in rare cases, small bowel cancer.

My view, as someone with coeliac disease

By Alice Fuller, Senior Health Reporter

WE all know that Ravneet Gill, Jo Brand and Jonathan Ross were joking.

And it was funny, as eating gluten when you have coeliac disease really can make a mess!

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But while I can laugh, it is also incredibly disappointing.

As someone with the condition, I can’t tell you how frustrating it is when people just don’t get it.

I have my own toaster, butter and jam, I use a separate chopping board, and I avoid anything labelled ‘may contain gluten’ or ‘made in a factory that handles gluten’.

I also have to do extensive research when going out for dinner and I always carry a cereal bar in my bag in case I can’t find anywhere safe to eat.

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It’s a nightmare, and when people make light of eating bread when it could make you seriously ill, it only adds to the misunderstanding.

Coeliac disease is serious, and it needs to be taken seriously.

“It is crucial to emphasise that coeliac disease is not a food preference or an allergy; it is a serious medical condition that requires lifelong adherence to a strict gluten free diet.

“We are particularly disheartened by Gill’s comments given her previous role as a judge on the Junior Bake Off, where she displayed compassion for those that have been diagnosed.

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“The remarks made during An Extra Slice perpetuate a narrative that dismisses the severity of this condition.

“They suggest that individuals with coeliac disease and the physical and mental health implications of adhering to a gluten free diet.

I want to make it really clear that my intention was not in any way to to downplay coeliac disease at all

Ravneet GillChef

“Discussions around gluten free diets should promote accurate understanding, respect, and accommodation for dietary needs rather than downplaying their significance.

“We are hopeful that this incident will encourage your team to engage in respectful conversations regarding coeliac disease and its impact on individuals and families.

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“We would appreciate the opportunity to discuss this matter further and provide accurate information about coeliac disease to ensure a more informed dialogue in future broadcasts.

“We kind request that you consider issuing an apology to people with coeliac disease on air to address the dismissive and inaccurate portrayal of coeliac disease presented in your programme.

“Thank you for your attention to this important matter. We look forward to your response.”

Gill said she will try to “think more carefully” before speaking on TV again.

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Channel 4 has been approached for comment.

Gill is a pastry chef, author and Junior Bake Off judge

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Gill is a pastry chef, author and Junior Bake Off judgeCredit: Getty

Vanessa Feltz faced similar backlash after comments she made on This Morning last year.

More than 2,000 complaints were made to Ofcom after saying a caller’s mother-in-law not allowing them to bring their own food to a gluten free Christmas dinner was “completely unreasonable”.

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“She’s treating coeliac disease as if it’s a potentially fatal peanut allergy and they can’t have anything with gluten in the house,” Feltz added.

The 61-year-old later apologised on her TalkTV show, saying she was “very sorry”.

What is coeliac disease and what are the main symptoms?

COELIAC disease is an autoimmune condition that affects one in 100 people in the UK – though many remain undiagnosed.

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When someone who has it eats gluten, their immune system attacks their own tissues, which damages their gut.

The symptoms vary from person to person and can range from very mild to severe.

But the most common signs include:

  • Severe or occasional diarrhoea, excessive wind and/or constipation
  • Persistent or unexplained nausea and vomiting
  • Recurrent stomach pain, cramping or bloating
  • Any combination of iron, vitamin B12 or folic acid deficiency
  • Anaemia
  • Tiredness
  • Sudden or unexpected weight loss
  • Mouth ulcers
  • Skin rash (dermatitis herpetiformis)
  • Tooth enamel problems
  • Liver abnormalities
  • Unexplained subfertility
  • Repeated miscarriages
  • Neurological (nerve) problems such as ataxia (loss of coordination, poor balance) and peripheral neuropathy (numbness and tingling in the hands and feet)

There is no cure. The only way to manage coeliac disease is with a strict gluten free diet.

This means eating no wheat, rye, barley and oats.

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Potential long-term complications include osteoporosis, iron deficiency anaemia, vitamin B12 or folate deficiency anaemia, bowel cancer and fertility issues.

Source: Coeliac UK and NHS

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