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How to cope with an eating disorder at Christmas – Herald Planet

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Katie Scott

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Katie Scott, bottom left, celebrates Christmas in 2017 with mum Hazel, brother Ben, and grandparents, Anne and John

Christmas celebrations in the UK often centre on food, drink and family gatherings, but campaigners warn that the party season can place additional strain on those living with eating disorders.

“It’s tricky even years down the line to watch the happiness and festivities at Christmas,” says Katie Scott, 21, who is in recovery from an eating disorder.

“I have always loved [the time of year] – I love the food, I love being with my family. But now it’s difficult because of the eating disorder.”

She adds: “No matter how hard I try or want it to be carefree or eating-disorder free I know that it can’t be – it’s bittersweet.”

Her comments come as new guidance is published to help those living with eating disorders over the festive season.

Katie first became unwell at the age of 14, restricting her food intake and falling into depression. She was initially diagnosed with eating disorder not otherwise specified (EDNOS), and later with anorexia aged 16.

She describes her first diagnosis as the beginning of a “long and ongoing struggle” with eating and her weight, mood and self-harm, straining her relationships with her family and friends.

“It left me feeling desperate and isolated,” she says. “It was a life-threatening situation.”

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Katie Scott

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Katie, who is in recovery, is now in her third year at university

Katie dropped out of school for periods of time, undergoing inpatient treatment. She was finally discharged from hospital aged 18, joining the year below her at school to finish her education before going to university.

“I had to rebuild my life from rock bottom,” she says.

Katie explains that she has found Christmas “an especially difficult time” both while unwell and in recovery, often feeling unable to get fully involved with the festivities.

“The celebrations are obviously very focused around food,” she says. “I love food, but I’m scared of it so I have this contradiction – the fear factor.

“I’ve found Christmas quite hard to deal with in the past because I wanted to look forward to it, but all of the elements that I love [about it] became stressful and scary.”

She adds: “I think anorexia might be an extreme version of losing the magic of Christmas. It’s still a lovely time of year but it’s not quite the same.

“I kid myself each year that it will be but it’s never as easy as it was before. It can be disappointing.”

The charity Beat estimates 1.25 million people in the UK have an eating disorder, with anorexia known to have the highest mortality rate of any mental illness.



Offering support at Christmas

The NHS and eating disorder charity Beat have published new guidance on how to support people with eating disorders and their families at Christmas.

The advice aims to help friends and family of those of any age with such an illness navigate the festive period – while continuing to manage a condition.

Some of the suggested techniques, based on experience from clinicians, patients and parents, include:

  • Serving food as a buffet rather than as sit-down meals
  • Minimising the social expectations of people with eating disorders over the festive season
  • Treating meals on and around Christmas Day as routinely as possible
  • Planning well ahead and thinking about how food features in the day
  • Once dinner is over, shifting the focus on to other activities such as playing games
  • Making loved ones aware to avoid questions about weight or appetite

For Katie, planning the structure of the day is key, including what she will do if she is feeling stressed – whether that is stepping outside or going for a walk.

She also advises finding someone to confide in. “Try and have one person who is at least aware that you might struggle,” she says.

Beat has also published advice on how to spot the signs of an eating disorder on its website.



Katie says the Christmas period can also be a hard time for her mother, who, she notices, is focused on keeping her safe and feeling OK amid the celebrations.

“She’s had a few very difficult Christmases with me,” Katie says. “It’s almost worse for mum because she has to deal with me and can’t anticipate how I’m going to react.”

Dr Prathiba Chitsabesan, NHS associate clinical director for children and young people’s mental health, says supporting families to manage eating disorders at home is “crucial”.

She adds that the “added pressure of New Year’s resolutions and the bombardment of weight loss messaging” so close to Christmas can prove challenging for those living with an eating disorder.

“Hopefully these tips will really make a difference,” she says.

‘Added pressures’

Caroline Price, Beat’s director of services, has warned that the pressure to eat large amounts at Christmas “can be triggering” for people with binge-eating disorder and bulimia, as well as causing anxiety for people with anorexia.

She says: “People with eating disorders often try to hide their illness and at Christmas when eating is a social occasion – often with people who they do not see frequently – they may feel ashamed and want to isolate themselves from others.

“At the same time, Christmas can be a source of distress for families who are caring for someone with an eating disorder.

“All these pressures can be made more difficult as the normal support networks are often not available at Christmas, as friends may be away, and regular social activities close for the holidays.”

Anyone worried about their own or someone else’s health is urged to contact Beat’s helplines, which are open year-round and every day from 16:00 to 20:00 GMT from 24 December to 1 January.

Those in need of support can get in contact via phone, email, anonymous one-to-one webchat or social media messaging.

  • Beat’s adult helpline can be reached on 0808 801 0677, or there is a dedicated Youthline for under-18s on 0808 801 0711. The online support groups and one-to-one webchat can be accessed here.

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Canada to donate up to 200,000 vaccine doses to combat mpox outbreaks in Africa

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The Canadian government says it will donate up to 200,000 vaccine doses to fight the mpox outbreak in Congo and other African countries.

It says the donated doses of Imvamune will come from Canada’s existing supply and will not affect the country’s preparedness for mpox cases in this country.

Minister of Health Mark Holland says the donation “will help to protect those in the most affected regions of Africa and will help prevent further spread of the virus.”

Dr. Madhukar Pai, Canada research chair in epidemiology and global health, says although the donation is welcome, it is a very small portion of the estimated 10 million vaccine doses needed to control the outbreak.

Vaccine donations from wealthier countries have only recently started arriving in Africa, almost a month after the World Health Organization declared the mpox outbreak a public health emergency of international concern.

A few days after the declaration in August, Global Affairs Canada announced a contribution of $1 million for mpox surveillance, diagnostic tools, research and community awareness in Africa.

On Thursday, the Africa Centres for Disease Control and Prevention said mpox is still on the rise and that testing rates are “insufficient” across the continent.

Jason Kindrachuk, Canada research chair in emerging viruses at the University of Manitoba, said donating vaccines, in addition to supporting surveillance and diagnostic tests, is “massively important.”

But Kindrachuk, who has worked on the ground in Congo during the epidemic, also said that the international response to the mpox outbreak is “better late than never (but) better never late.”

“It would have been fantastic for us globally to not be in this position by having provided doses a much, much longer time prior than when we are,” he said, noting that the outbreak of clade I mpox in Congo started in early 2023.

Clade II mpox, endemic in regions of West Africa, came to the world’s attention even earlier — in 2022 — as that strain of virus spread to other countries, including Canada.

Two doses are recommended for mpox vaccination, so the donation may only benefit 100,000 people, Pai said.

Pai questioned whether Canada is contributing enough, as the federal government hasn’t said what percentage of its mpox vaccine stockpile it is donating.

“Small donations are simply not going to help end this crisis. We need to show greater solidarity and support,” he said in an email.

“That is the biggest lesson from the COVID-19 pandemic — our collective safety is tied with that of other nations.”

This report by The Canadian Press was first published Sept. 13, 2024.

Canadian Press health coverage receives support through a partnership with the Canadian Medical Association. CP is solely responsible for this content.

The Canadian Press. All rights reserved.

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How many Nova Scotians are on the doctor wait-list? Number hit 160,000 in June

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HALIFAX – The Nova Scotia government says it could be months before it reveals how many people are on the wait-list for a family doctor.

The head of the province’s health authority told reporters Wednesday that the government won’t release updated data until the 160,000 people who were on the wait-list in June are contacted to verify whether they still need primary care.

Karen Oldfield said Nova Scotia Health is working on validating the primary care wait-list data before posting new numbers, and that work may take a matter of months. The most recent public wait-list figures are from June 1, when 160,234 people, or about 16 per cent of the population, were on it.

“It’s going to take time to make 160,000 calls,” Oldfield said. “We are not talking weeks, we are talking months.”

The interim CEO and president of Nova Scotia Health said people on the list are being asked where they live, whether they still need a family doctor, and to give an update on their health.

A spokesperson with the province’s Health Department says the government and its health authority are “working hard” to turn the wait-list registry into a useful tool, adding that the data will be shared once it is validated.

Nova Scotia’s NDP are calling on Premier Tim Houston to immediately release statistics on how many people are looking for a family doctor. On Tuesday, the NDP introduced a bill that would require the health minister to make the number public every month.

“It is unacceptable for the list to be more than three months out of date,” NDP Leader Claudia Chender said Tuesday.

Chender said releasing this data regularly is vital so Nova Scotians can track the government’s progress on its main 2021 campaign promise: fixing health care.

The number of people in need of a family doctor has more than doubled between the 2021 summer election campaign and June 2024. Since September 2021 about 300 doctors have been added to the provincial health system, the Health Department said.

“We’ll know if Tim Houston is keeping his 2021 election promise to fix health care when Nova Scotians are attached to primary care,” Chender said.

This report by The Canadian Press was first published Sept. 11, 2024.

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Newfoundland and Labrador monitoring rise in whooping cough cases: medical officer

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ST. JOHN’S, N.L. – Newfoundland and Labrador‘s chief medical officer is monitoring the rise of whooping cough infections across the province as cases of the highly contagious disease continue to grow across Canada.

Dr. Janice Fitzgerald says that so far this year, the province has recorded 230 confirmed cases of the vaccine-preventable respiratory tract infection, also known as pertussis.

Late last month, Quebec reported more than 11,000 cases during the same time period, while Ontario counted 470 cases, well above the five-year average of 98. In Quebec, the majority of patients are between the ages of 10 and 14.

Meanwhile, New Brunswick has declared a whooping cough outbreak across the province. A total of 141 cases were reported by last month, exceeding the five-year average of 34.

The disease can lead to severe complications among vulnerable populations including infants, who are at the highest risk of suffering from complications like pneumonia and seizures. Symptoms may start with a runny nose, mild fever and cough, then progress to severe coughing accompanied by a distinctive “whooping” sound during inhalation.

“The public, especially pregnant people and those in close contact with infants, are encouraged to be aware of symptoms related to pertussis and to ensure vaccinations are up to date,” Newfoundland and Labrador’s Health Department said in a statement.

Whooping cough can be treated with antibiotics, but vaccination is the most effective way to control the spread of the disease. As a result, the province has expanded immunization efforts this school year. While booster doses are already offered in Grade 9, the vaccine is now being offered to Grade 8 students as well.

Public health officials say whooping cough is a cyclical disease that increases every two to five or six years.

Meanwhile, New Brunswick’s acting chief medical officer of health expects the current case count to get worse before tapering off.

A rise in whooping cough cases has also been reported in the United States and elsewhere. The Pan American Health Organization issued an alert in July encouraging countries to ramp up their surveillance and vaccination coverage.

This report by The Canadian Press was first published Sept. 10, 2024.

The Canadian Press. All rights reserved.

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