Latest news with #ALS
The Citizen
5 hours ago
- The Citizen
Man killed in Pinetown head-on collision
A MAN believed to be in his 30s was died following a head-on collision on the M7 last night, Friday, June 27. The accident, which left two other people injured, happened on the Durban-bound lane near the Winston Churchill offramp in the Pinetown area. Also read: Man dies in early morning Westville accident ALS Paramedics spokesperson Garrith Jamieson said paramedics arrived on the scene just before 21:30 to find the badly damaged vehicles on the busy roadway. According to Jamieson, it is alleged that the one vehicle crossed the centre median and collided head-on into a bakkie. 'The bakkie then rolled, coming to rest on its side. Paramedics quickly assessed the scene and found that the light motor vehicle driver was entrapped in the wreckage. 'Paramedics assessed the man, however he showed no signs of life and was declared deceased on the scene. The two occupants from the bakkie had left the scene to hospital before paramedics' arrival,' said Jamieson. He added that police will investigate the cause of the accident. For more from the Highway Mail, follow us on Facebook , X and Instagram. You can also check out our videos on our YouTube channel or follow us on TikTok. Click to subscribe to our newsletter here At Caxton, we employ humans to generate daily fresh news, not AI intervention. Happy reading!
Hamilton Spectator
17 hours ago
- Politics
- Hamilton Spectator
Canada's national anthem is 45 years old today
OTTAWA - While the country will celebrate it's birthday next week, O Canada got a head start on Friday, celebrating its 45th year as the official national anthem. While it was often used as the de facto national anthem for years, O Canada was officially adopted through the National Anthem Act on June 27, 1980. A few days later, on Canada Day, the Act was proclaimed by Gov. Gen. Edward Schreyer at a public ceremony on Parliament Hill in front of thousands of Canadians, making O Canada an official national symbol. The song actually has existed for more than a century, though its lyrics have changed several times over the decades. Commissioned to mark Saint-Jean-Baptiste Day celebrations in Québec on June 24, 1880, O Canada's music was composed by Calixa Lavallée and its French lyrics were written by Adolphe-Basile Routhier. While many different English versions of the song emerged as it grew in popularity across the country, the most well-known English lyrics were written in 1908 by Robert Stanley Weir, a lawyer and judge. The Government of Canada website says the lyrics of the official French version have remained unchanged since 1880. Weir's English lyrics underwent several modifications over the decades on their way to becoming the official English version. Previous versions of the song included closing lines like 'Defend our rights, forfend this nation's thrall' and 'Bless our dear land this day and evermore.' Some lines were changed more than once. In 1913 the original line 'True patriot love thou dost in us command' became 'True patriot love in all thy sons command.' In 2018 that line changed again to 'in all of us command.' The Canadian Encyclopedia says discussions about discriminatory aspects of the anthem, including the gender-exclusive use of the word 'sons,' began in the 1950s. Former Liberal member of Parliament Mauril Bélanger, who pushed to drop 'sons' from the lyrics for years while battling ALS, introduced a private member's bill in 2016 to change the line. It was approved in the House of Commons as Bill C-210 a month later by a vote of 225 to 74. It wasn't until 2018 — after several debates in the Senate and after Bélanger had passed away — that the change became official when the bill became law. The new gender-neutral lyric received mixed reviews and Conservative senators abstained from the final vote in 2018. While the original manuscript of 'O Canada' no longer exists, there are two copies of the first edition. One is held in the archives of the Séminaire de Québec and the other is at the Université de Montréal. This report by The Canadian Press was first published June 27, 2025. Error! Sorry, there was an error processing your request. There was a problem with the recaptcha. Please try again. You may unsubscribe at any time. By signing up, you agree to our terms of use and privacy policy . This site is protected by reCAPTCHA and the Google privacy policy and terms of service apply. Want more of the latest from us? Sign up for more at our newsletter page .
Winnipeg Free Press
17 hours ago
- Politics
- Winnipeg Free Press
Canada's national anthem is 45 years old today
OTTAWA – While the country will celebrate it's birthday next week, O Canada got a head start on Friday, celebrating its 45th year as the official national anthem. While it was often used as the de facto national anthem for years, O Canada was officially adopted through the National Anthem Act on June 27, 1980. A few days later, on Canada Day, the Act was proclaimed by Gov. Gen. Edward Schreyer at a public ceremony on Parliament Hill in front of thousands of Canadians, making O Canada an official national symbol. The song actually has existed for more than a century, though its lyrics have changed several times over the decades. Commissioned to mark Saint-Jean-Baptiste Day celebrations in Québec on June 24, 1880, O Canada's music was composed by Calixa Lavallée and its French lyrics were written by Adolphe-Basile Routhier. While many different English versions of the song emerged as it grew in popularity across the country, the most well-known English lyrics were written in 1908 by Robert Stanley Weir, a lawyer and judge. The Government of Canada website says the lyrics of the official French version have remained unchanged since 1880. Weir's English lyrics underwent several modifications over the decades on their way to becoming the official English version. Previous versions of the song included closing lines like 'Defend our rights, forfend this nation's thrall' and 'Bless our dear land this day and evermore.' Some lines were changed more than once. In 1913 the original line 'True patriot love thou dost in us command' became 'True patriot love in all thy sons command.' In 2018 that line changed again to 'in all of us command.' The Canadian Encyclopedia says discussions about discriminatory aspects of the anthem, including the gender-exclusive use of the word 'sons,' began in the 1950s. Former Liberal member of Parliament Mauril Bélanger, who pushed to drop 'sons' from the lyrics for years while battling ALS, introduced a private member's bill in 2016 to change the line. It was approved in the House of Commons as Bill C-210 a month later by a vote of 225 to 74. It wasn't until 2018 — after several debates in the Senate and after Bélanger had passed away — that the change became official when the bill became law. The new gender-neutral lyric received mixed reviews and Conservative senators abstained from the final vote in 2018. While the original manuscript of 'O Canada' no longer exists, there are two copies of the first edition. One is held in the archives of the Séminaire de Québec and the other is at the Université de Montréal. This report by The Canadian Press was first published June 27, 2025.
The Star
a day ago
- Entertainment
- The Star
Eric Dane, who famously bathed with 2 women, now appears tangled up with 3
US actor Eric Dane and filmmaker Janell Shirtcliff attend Prime Video's 'Countdown' premiere at the Harmony Gold theatre in Los Angeles on June 18, 2025. Photo: AFP Eric Dane and filmmaker Janell Shirtcliff looked to be in full couple mode Wednesday (June 18) at the premiere of Prime Video's Countdown , a new series he stars in with Jensen Ackles. Hands were held; smiles and admiring glances were exchanged. He was definitely not with Rebecca Gayheart, whom he married in October 2004 and just said – on national news, no less – is the person he reaches out to daily for 'stalwart' support. Nope, even though Gayheart in early March requested the dismissal, without prejudice, of the 2018 divorce petition she had filed against Dane. Dane revealed in April that he had been diagnosed with amyotrophic lateral sclerosis, aka ALS, or Lou Gehrig's disease. Earlier last week, he revealed that he had lost function in his right arm due to the neuromuscular disease and felt his left arm failing. So who's dating whom? Dane's relationship status is a bit fuzzy. The Grey's Anatomy alum, 52, has been 'in an on-and-off relationship' with Shirtcliff for more than three years, Entertainment Tonight reported Wednesday. The two 'care deeply for each other,' the outlet said, citing a source who added, 'Eric asked Janell to be there for him during this time, and she wanted to show up for him.' Shirtcliff, who is a photographer and director, is in preproduction on the film Generation Angst and postproduction on the horror flick Triton , according to IMDb. But – Dane's alleged girlfriend, actor Priya Jain, 27, was 'blindsided' by his appearance at the event with Shirtcliff, 41, a source told Page Six on Thursday. Jain and Dane met last summer and became 'exclusive' in November 2024, the source said. 'They never broke up.' The two have been photographed arm-in-arm in public and have matching tattoos, and she has spent 'almost every night' at his house since they coupled up, Page Six said. They reportedly were together last weekend. This three-way confusion is a tiny bit reminiscent of Dane and Gayheart's nude 2009 bathtub video with actor Kari Ann Peniche, which Dane discussed in 2019 with Glamour. In the leaked video, the three could be seen bathing together naked – not having sex – and discussing their potential porn names about 15 years into the Gayheart-Dane marriage. 'I don't necessarily think I was breaking any laws and corrupting anybody. We were just three people taking a bath,' he told the magazine. He added, referring at the time to the entirety of his past – including the bathtub video and his addiction to prescribed painkillers – 'I have no regrets nor do I make any apologies for my life experience. It's my life experience and I am at peace with all of it.' As for Gayheart, she and Dane remain estranged as husband and wife even though she called off the divorce and they are in frequent contact as co-parents of their two daughters. 'I call Rebecca. I talk to her every day,' Dane said on a recent episode of Good Morning America , fighting back tears as he talked about battling ALS. 'We have managed to become better friends and better parents. And she is probably my biggest champion, my most stalwart supporter, and I lean on her.' – Los Angeles Times/Tribune News Service
The Advertiser
a day ago
- Health
- The Advertiser
How Graham is tackling life, one year after he was diagnosed with an incurable disease
A year ago, Graham Lancaster received news that could have completely upended his life. The well-known regional lawyer was told he had the incurable degenerative condition motor neurone disease (MND). It's something he is conscious of every day, and he is proactive in taking steps to try and slow the disease's progression. But generally, life has rolled on: he continues to work, indulge in his interests, and maintain his sense of humour, although he admits it can slant a little dark sometimes. "The concept of the one-year anniversary coming up is significant because, in that time, I haven't had a lot of symptoms and my progression has been very slow, and the doctors have confirmed that," Mr Lancaster said. There are reminders of the illness: the morning he spoke to the Mercury, his tricep started twitching, a symptom of MND. "I went, 'Alright, you're reminding me you're still there', " he said. Mr Lancaster received a provisional diagnosis of MND, an incurable degenerative illness, on June 24, 2024, after he pushed for tests when he realised he had muscle wasting in his right hand. That blow came just days after Global MND Awareness Day, which is marked annually on June 21. Ten days after the provisional diagnosis, doctors confirmed Mr Lancaster had sporadic amyotrophic lateral sclerosis (ALS), a form of the disease for which the cause is not known. Mr Lancaster is receiving treatment from his doctors, including a trial of a drug called Ambroxol, and has appointments every three months to track the progression of his illness. But he is also on a regimen of vitamin supplements and other therapies, which he has found through online communities and his own searches, which he hopes will inhibit the disease's progression. Mr Lancaster said the number of people who died of MND within a year or two of diagnosis suggested to him that "late diagnosis is a very real problem". MND Australia says the average survival time after diagnosis is two and a half years. "I was lucky to get diagnosed early, so I got on to doing things early, and you know, I do believe that has helped to slow the progression," Mr Lancaster said. "If you get diagnosed late, you're already on a pathway of cascading issues and problems, and it's hard to turn all of that back and climb your way back up from that." Mr Lancaster plans to beat the expected survival period of two to five years. Not only has he taken steps to slow the MND, but he has put more energy into improving his general health. Unfortunately, he had to give up cheer - at one point, he was Australia's oldest male cheerleader - because he doesn't want to let his team down should he become unable to attend competitions. But as a dedicated supporter of the Illawarra Hawks, Mr Lancaster has remained a prominent sight at the basketball team's home games since his diagnosis, always sporting his distinctive double-horned red-and-black Vikings hat. "I will be going to the Hawks games for as long as I can," he said. "The seat we have at the stadium, if I've got to crawl down to that seat, I will crawl down to that seat and crawl back up the steps." "As far as purpose, I think that having a job that I love means that I get in, I get things done, and that keeps me going as well," Mr Lancaster said. He also has another very special motivating factor: he and his wife, Cath, will become grandparents for the first time later this year when their daughter Sarah (they also have a son, Patrick) welcomes her first child with husband Jordan. Mr Lancaster said Cath had supported his efforts to slow his disease - but added that she didn't let him get out of jobs around the house just because he had MND. His goal is not just to live as long as he can, but to live well and help others. To that end, he shares information he's learnt with others experiencing MND and offers support. "I've come to embrace the ALS," he said. "I don't want to spend a lot of energy fighting it, per se. I think I'm working with it, and it's just something that's part of the day now." A year ago, Graham Lancaster received news that could have completely upended his life. The well-known regional lawyer was told he had the incurable degenerative condition motor neurone disease (MND). It's something he is conscious of every day, and he is proactive in taking steps to try and slow the disease's progression. But generally, life has rolled on: he continues to work, indulge in his interests, and maintain his sense of humour, although he admits it can slant a little dark sometimes. "The concept of the one-year anniversary coming up is significant because, in that time, I haven't had a lot of symptoms and my progression has been very slow, and the doctors have confirmed that," Mr Lancaster said. There are reminders of the illness: the morning he spoke to the Mercury, his tricep started twitching, a symptom of MND. "I went, 'Alright, you're reminding me you're still there', " he said. Mr Lancaster received a provisional diagnosis of MND, an incurable degenerative illness, on June 24, 2024, after he pushed for tests when he realised he had muscle wasting in his right hand. That blow came just days after Global MND Awareness Day, which is marked annually on June 21. Ten days after the provisional diagnosis, doctors confirmed Mr Lancaster had sporadic amyotrophic lateral sclerosis (ALS), a form of the disease for which the cause is not known. Mr Lancaster is receiving treatment from his doctors, including a trial of a drug called Ambroxol, and has appointments every three months to track the progression of his illness. But he is also on a regimen of vitamin supplements and other therapies, which he has found through online communities and his own searches, which he hopes will inhibit the disease's progression. Mr Lancaster said the number of people who died of MND within a year or two of diagnosis suggested to him that "late diagnosis is a very real problem". MND Australia says the average survival time after diagnosis is two and a half years. "I was lucky to get diagnosed early, so I got on to doing things early, and you know, I do believe that has helped to slow the progression," Mr Lancaster said. "If you get diagnosed late, you're already on a pathway of cascading issues and problems, and it's hard to turn all of that back and climb your way back up from that." Mr Lancaster plans to beat the expected survival period of two to five years. Not only has he taken steps to slow the MND, but he has put more energy into improving his general health. Unfortunately, he had to give up cheer - at one point, he was Australia's oldest male cheerleader - because he doesn't want to let his team down should he become unable to attend competitions. But as a dedicated supporter of the Illawarra Hawks, Mr Lancaster has remained a prominent sight at the basketball team's home games since his diagnosis, always sporting his distinctive double-horned red-and-black Vikings hat. "I will be going to the Hawks games for as long as I can," he said. "The seat we have at the stadium, if I've got to crawl down to that seat, I will crawl down to that seat and crawl back up the steps." "As far as purpose, I think that having a job that I love means that I get in, I get things done, and that keeps me going as well," Mr Lancaster said. He also has another very special motivating factor: he and his wife, Cath, will become grandparents for the first time later this year when their daughter Sarah (they also have a son, Patrick) welcomes her first child with husband Jordan. Mr Lancaster said Cath had supported his efforts to slow his disease - but added that she didn't let him get out of jobs around the house just because he had MND. His goal is not just to live as long as he can, but to live well and help others. To that end, he shares information he's learnt with others experiencing MND and offers support. "I've come to embrace the ALS," he said. "I don't want to spend a lot of energy fighting it, per se. I think I'm working with it, and it's just something that's part of the day now." A year ago, Graham Lancaster received news that could have completely upended his life. The well-known regional lawyer was told he had the incurable degenerative condition motor neurone disease (MND). It's something he is conscious of every day, and he is proactive in taking steps to try and slow the disease's progression. But generally, life has rolled on: he continues to work, indulge in his interests, and maintain his sense of humour, although he admits it can slant a little dark sometimes. "The concept of the one-year anniversary coming up is significant because, in that time, I haven't had a lot of symptoms and my progression has been very slow, and the doctors have confirmed that," Mr Lancaster said. There are reminders of the illness: the morning he spoke to the Mercury, his tricep started twitching, a symptom of MND. "I went, 'Alright, you're reminding me you're still there', " he said. Mr Lancaster received a provisional diagnosis of MND, an incurable degenerative illness, on June 24, 2024, after he pushed for tests when he realised he had muscle wasting in his right hand. That blow came just days after Global MND Awareness Day, which is marked annually on June 21. Ten days after the provisional diagnosis, doctors confirmed Mr Lancaster had sporadic amyotrophic lateral sclerosis (ALS), a form of the disease for which the cause is not known. Mr Lancaster is receiving treatment from his doctors, including a trial of a drug called Ambroxol, and has appointments every three months to track the progression of his illness. But he is also on a regimen of vitamin supplements and other therapies, which he has found through online communities and his own searches, which he hopes will inhibit the disease's progression. Mr Lancaster said the number of people who died of MND within a year or two of diagnosis suggested to him that "late diagnosis is a very real problem". MND Australia says the average survival time after diagnosis is two and a half years. "I was lucky to get diagnosed early, so I got on to doing things early, and you know, I do believe that has helped to slow the progression," Mr Lancaster said. "If you get diagnosed late, you're already on a pathway of cascading issues and problems, and it's hard to turn all of that back and climb your way back up from that." Mr Lancaster plans to beat the expected survival period of two to five years. Not only has he taken steps to slow the MND, but he has put more energy into improving his general health. Unfortunately, he had to give up cheer - at one point, he was Australia's oldest male cheerleader - because he doesn't want to let his team down should he become unable to attend competitions. But as a dedicated supporter of the Illawarra Hawks, Mr Lancaster has remained a prominent sight at the basketball team's home games since his diagnosis, always sporting his distinctive double-horned red-and-black Vikings hat. "I will be going to the Hawks games for as long as I can," he said. "The seat we have at the stadium, if I've got to crawl down to that seat, I will crawl down to that seat and crawl back up the steps." "As far as purpose, I think that having a job that I love means that I get in, I get things done, and that keeps me going as well," Mr Lancaster said. He also has another very special motivating factor: he and his wife, Cath, will become grandparents for the first time later this year when their daughter Sarah (they also have a son, Patrick) welcomes her first child with husband Jordan. Mr Lancaster said Cath had supported his efforts to slow his disease - but added that she didn't let him get out of jobs around the house just because he had MND. His goal is not just to live as long as he can, but to live well and help others. To that end, he shares information he's learnt with others experiencing MND and offers support. "I've come to embrace the ALS," he said. "I don't want to spend a lot of energy fighting it, per se. I think I'm working with it, and it's just something that's part of the day now." A year ago, Graham Lancaster received news that could have completely upended his life. The well-known regional lawyer was told he had the incurable degenerative condition motor neurone disease (MND). It's something he is conscious of every day, and he is proactive in taking steps to try and slow the disease's progression. But generally, life has rolled on: he continues to work, indulge in his interests, and maintain his sense of humour, although he admits it can slant a little dark sometimes. "The concept of the one-year anniversary coming up is significant because, in that time, I haven't had a lot of symptoms and my progression has been very slow, and the doctors have confirmed that," Mr Lancaster said. There are reminders of the illness: the morning he spoke to the Mercury, his tricep started twitching, a symptom of MND. "I went, 'Alright, you're reminding me you're still there', " he said. Mr Lancaster received a provisional diagnosis of MND, an incurable degenerative illness, on June 24, 2024, after he pushed for tests when he realised he had muscle wasting in his right hand. That blow came just days after Global MND Awareness Day, which is marked annually on June 21. Ten days after the provisional diagnosis, doctors confirmed Mr Lancaster had sporadic amyotrophic lateral sclerosis (ALS), a form of the disease for which the cause is not known. Mr Lancaster is receiving treatment from his doctors, including a trial of a drug called Ambroxol, and has appointments every three months to track the progression of his illness. But he is also on a regimen of vitamin supplements and other therapies, which he has found through online communities and his own searches, which he hopes will inhibit the disease's progression. Mr Lancaster said the number of people who died of MND within a year or two of diagnosis suggested to him that "late diagnosis is a very real problem". MND Australia says the average survival time after diagnosis is two and a half years. "I was lucky to get diagnosed early, so I got on to doing things early, and you know, I do believe that has helped to slow the progression," Mr Lancaster said. "If you get diagnosed late, you're already on a pathway of cascading issues and problems, and it's hard to turn all of that back and climb your way back up from that." Mr Lancaster plans to beat the expected survival period of two to five years. Not only has he taken steps to slow the MND, but he has put more energy into improving his general health. Unfortunately, he had to give up cheer - at one point, he was Australia's oldest male cheerleader - because he doesn't want to let his team down should he become unable to attend competitions. But as a dedicated supporter of the Illawarra Hawks, Mr Lancaster has remained a prominent sight at the basketball team's home games since his diagnosis, always sporting his distinctive double-horned red-and-black Vikings hat. "I will be going to the Hawks games for as long as I can," he said. "The seat we have at the stadium, if I've got to crawl down to that seat, I will crawl down to that seat and crawl back up the steps." "As far as purpose, I think that having a job that I love means that I get in, I get things done, and that keeps me going as well," Mr Lancaster said. He also has another very special motivating factor: he and his wife, Cath, will become grandparents for the first time later this year when their daughter Sarah (they also have a son, Patrick) welcomes her first child with husband Jordan. Mr Lancaster said Cath had supported his efforts to slow his disease - but added that she didn't let him get out of jobs around the house just because he had MND. His goal is not just to live as long as he can, but to live well and help others. To that end, he shares information he's learnt with others experiencing MND and offers support. "I've come to embrace the ALS," he said. "I don't want to spend a lot of energy fighting it, per se. I think I'm working with it, and it's just something that's part of the day now."
