P.E.I. announces Children's Summer Food Program
Minister of Social Development and Seniors Barb Ramsay (centre), joins (from left to right) Chef Kevin Bottrill, Betsy Cormier, Duke Cormier, and Chef Steve Gallant from Fiveeleven West in Summerside. (Source: Government of P.E.I.)
Prince Edward Island announced it will support the Children's Summer Food Program for 2025.
The Children's Summer Food Program, established in 2021, is primarily intended for families currently receiving financial support through social assistance or assured income programs.
The program delivers five nutritious frozen meals each week through July and August to children in households facing food insecurity, to fill the gap in between school food programs.
'We know there are Island families struggling to put food on the table in this time of high inflation and high food prices, and this program is an important part of our efforts to support them. As mandated by the Poverty Elimination Strategy Act, our government remains committed to addressing food insecurity in P.E.I. and we have made substantial efforts in this area,' said Barb Ramsay, minister of Social Development and Seniors.
With a budget investment of $600,000, the program prepares meals sourced from local restaurants and catering companies and delivers them to homes across the province, a release from the province said.
'We value our community, and all the support we've received over the years, so we strive to make a positive impact where we can,' said Duke Cormier, owner of Fiveelevenwest in Summerside, one of the food suppliers for the program. 'Knowing that we are helping families who are struggling, and giving kids the nutrition they need to be healthy makes us proud to be a part of this effort.'
Families not currently enrolled in social assistance or assured income programs but experiencing financial difficulties can apply through the registration form. Registration for the program begins Tuesday and will remain open for the duration of the program.
For more P.E.I. news, visit our dedicated provincial page.
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Globe and Mail
32 minutes ago
- Globe and Mail
To boost productivity, more young Canadians must go into the skilled trades
Interested in more careers-related content? Check out our new weekly Work Life newsletter. Sent every Monday afternoon. The spotlight is now on skilled trades and with good reason. Looking at the trends, the demand for workers will be high and the supply will be constrained, meaning potential shortages in many occupations for years to come. And, unlike the situation in traditional white-collar positions, jobs in the trades aren't likely to be replaced by artificial intelligence. Workers can't be trained overnight to fill needs, however, so the real question might be whether we will have enough skilled workers to meet the needs of a Canadian economy facing some major economic challenges. A May report on Canada by the Organisation for Economic Cooperation and Development (OECD) outlined some of the economic issues at stake in Canada. At the top of the list is Canadian productivity, which is close to the OECD average but well below that of many advanced nations including the United States. Added to that, similar to other countries, Canada will have to deal the reality of a changing climate, which will mean a need for 'green skills'. More specific for Canada is the need to build a substantial amount of new housing. For all of these challenges, the report sees having the right workers in place as being vital and that means having enough workers in the skilled trades. At the moment, however, the skilled trades are under-represented in the Canadian workforce. According to a 2024 report from Statistics Canada, the country leads the G7 in having the most educated workforce as measured by college and university graduates, but the same cannot be said for those in the trades. In fact, the number of working age apprenticeship certificate holders is falling. In 2021 (the last year for which data is available) there were 1.62 million tradespeople employed in Canada, a drop of 5.7 per cent from 2016. Although some of this was because of pandemic closures, the pandemic also caused record declines in those registering for training in the trades, which does not bode well for supply. With baby boomers and Gen Xers rapidly exiting the workforce, the number of vacancies in the trades is rising, suggesting any current skill shortages will only be amplified over time. The OECD estimates that between retirements and new demand Canada will have about 1.2 million job openings in the trades over the next decade, which will account for about 15 per cent of all job openings. The timing is right for young workers to take a good look at the trades. The May Labour Force Survey showed that the Canadian unemployment rate for youth aged 15 to 24 was 14.1 per cent, more than twice the 6.9 per cent rate for the overall labour force. The weakness in the market suggests that many young workers should be open to the idea of acquiring training in the trades. The OECD report lists that benefits of doing so include the fact that in Canada young adults with vocational secondary or post-secondary non-tertiary education out-earn their peers with a general education by about 25 per cent. An added bonus is that apprenticeships are typically paid, which means young workers can start their careers without student debt. As for AI, for the moment, it doesn't seem likely it will have a huge immediate effect on employment in the trades. To be sure there are many applications of AI that will change the nature of trades, from using AI software to diagnose plumbing problems to utilizing it for training. Completely replacing workers with robots or any kind of technology does not seem to be practical however and any impact would likely be more muted than for many other professions. If traditional white-collar jobs appear to be the ones most at risk of being replaced, skilled trades would be at the bottom of the list. Policy is slowly shifting to deal with the need for workers in the skilled trades although it might not be shifting quickly enough. In one of his first policy acts after taking office, Prime Minster Mark Carney announced a plan to support apprenticeship training with the release accompanying the announcement to say that 'The work of bricklayers, crane operators, welders and others are essential in building the future of Canada'. The OECD report recommends that Canada go much further to increase the supply of workers, starting with eliminating the differences between provincial regulations that make it difficult for workers to move between provinces. None of the concerns around the trades are actually new and we have known for decades that the demographics would mean a wave of retirements and the need for workers. Interestingly, that was supposed to happen for a wide range of occupations but technological shifts are changing that story in many cases. With the trades bucking that trend and with the economic need for skills so high, now would be the perfect time for the public and private sectors to do what it takes and entice the labour market to shift in the right direction.
CBC
32 minutes ago
- CBC
Hard to swallow
ALS patients and their families say they wasted tens of thousands of dollars and some of their last months on a Moose Jaw-based treatment program that failed to deliver what it promised Don Somers/CBC Geoff Leo Senior Investigative Journalist Jun. 13, 2025 Geoff Sando learned of his death sentence through an annoying conversation with his wife. In the summer of 2023, he and Teresa were out for a walk near their home south of Los Angeles. 'I started noticing that he was walking kinda strange,' Teresa told CBC. She mentioned it to Geoff. 'I was actually getting a little upset, if I'm being honest, that she was pointing it out,' Geoff recalled. But she was right. From that moment, his condition just got worse. For the next few months, he underwent tests, spoke with specialists and received treatments. Then, on March 15, 2024, his neurologist called him in for a meeting. The doctor told Geoff he has amyotrophic lateral sclerosis — ALS. 'It was pretty devastating when he tells you you have something that there is no cure for,' Geoff said. 'And you're just slowly going to die.' Eighty per cent of ALS patients die within five years. Just 10 per cent survive a decade. The ALS Society of Canada says there's no known cure, adding that while there are treatments available, 'most focus on symptom relief and do not significantly alter the progression of the disease.' 'Their plan of action was for you to go home and get your affairs in order because you're going to die in the next two to five years,' Geoff told CBC, breaking into tears. The news launched him on a desperate search for a cure that would lead him to a small facility in Moose Jaw, Sask., run by a man making stunning claims. Dayan Goodenowe, whose website refers to him as a world-renowned neuroscientist, says his supplements and treatment program can halt the progression of ALS symptoms and set patients on the path to recovery. 'There was no hesitation,' Geoff said. 'There was no other treatment that claimed it stopped progression that we could ever find.' Geoff and dozens of other ALS patients have spent tens of thousands of dollars and months of their time receiving Goodenow's treatment in Moose Jaw — treatment experts say is unsubstantiated, expensive and troubling. 'Here is a clinic in Canada offering an unproven — completely unproven — scientifically questionable therapy,' said Timothy Caufield, a University of Alberta law professor who specializes in the legal and ethical issues surrounding medical research. 'We absolutely need to have the regulatory mechanisms of policy levers to stop this kind of thing.' Goodenowe's claims spark hope Geoff was filled with fear and hopelessness after his diagnosis. But Teresa, who's a nurse, wasn't ready to concede. 'I told Geoff, 'Don't even say you have ALS. Don't own it. Something caused it. Let's figure out what triggered this,'' she said. That inspired hope and a hunt for a solution. 'There's got to be something out there that the FDA or medical science hasn't approved,' he said. 'When it's the alternative of just sitting around waiting to die, you are willing to try just about anything.' Geoff, a CEO of several companies in his mid-60s, was an active golfer and wakeboarder before his diagnosis. He devolved rapidly, from limping to a cane to a walker to a wheelchair. He lost his ability to type, feed himself or go to the bathroom without help. One day last summer, Teresa came across a YouTube video featuring Dayan Goodenowe. Geoff instantly recognized something different in his tone and his claims. In one video, Goodenowe says, "ALS is a serious disease, but it can be beaten.' In another, he says, 'Stopping the progression of ALS actually isn't that hard. It really is just biochemical math.' Goodenowe is not a medical doctor, but he does have a PhD in medical science with a focus on psychiatry. He's a listed author on dozens of academic papers on a range of topics, from Alzheimer's to cancer screening to mass spectrometry. Geoff decided to reach out. 'I got to try something and this guy seems to have the best idea out there.' The sales pitch Late last summer, Geoff and Teresa met with Goodenowe and his chief business officer, Tracy Zimmerman, on a series of video calls. Teresa recorded the calls and provided them to CBC. 'Geoff, we expect you to get stronger,' Zimmerman said. 'We have a 100 per cent success rate in stopping the progression and in restoring function of people with ALS.' Goodenowe echoed those claims, saying, 'It's clearly, unambiguously possible to get better.' 'How exciting is that?' Teresa asked Geoff. 'That is very exciting because if you go to the doctors here, you just get nothing but bad news,' Geoff replied. Goodenowe agreed with Geoff's critique of the medical industry, saying, 'They really do fail on diseases like ALS.' Michael Gieselman and his wife Shannon, also from Southern California, were checking out Goodenowe's program last summer as well. Michael, a 57-year-old sales director and former U.S. Navy pilot, was diagnosed with ALS in April 2022. His condition was quickly deteriorating. He had difficulty breathing, swallowing and speaking, and was unable to walk. Goodenowe offered hope. 'Even if you take a look at some individuals that were in worse case than you with loss of full hand movements, we get their muscle function back, we get their lung function back,' he told them in a video call. 'You are not going to die of ALS in our care,' Goodenowe told Michael. 'That's just the God's honest truth.' Zimmerman told them that the fix for ALS is actually well known in the scientific community. 'It's sad, but the scientists have actually known how to reverse ALS for decades,' she said. 'I'm not putting down pharma in any way, but … the same companies that profit off of you being sick are not going to be the companies that are going to bring you a cure, and anyone who believes that is deluding themselves.' 'There's been no progression whatsoever' The most persuasive part of the pitch for Michael was the testimonial offered by Corey Mitchell in a video on Goodenowe's website. It features the bearded 49-year-old telling his story of ALS recovery and saying the disease had completely stopped progressing. 'I'm starting to feel like time is on my side,' he says in the video, with a scratchy voice. Michael was sold, but Shannon was skeptical. She asked to speak with Mitchell and his partner Jennifer about the treatment, but after the phone call, she remained unpersuaded. 'I didn't believe any of it,' she told CBC. She said she was frustrated by Michael's gullibility. 'I could barely restrain myself. How can my husband believe?' she asked herself. 'My husband is the most skeptical person on the planet. But this is what's so sad about the whole thing. That's how desperate these poor people with this disease are.' Michael signed up for Goodenowe's home delivery program: four months of supplements shipped to his house, supported by staff who conducted regular testing and provided advice. On the call, Shannon and Michael explained that they weren't certain he would survive until the end of the four-month program. They asked if the price could be pro-rated on a month-by-month basis. Goodenowe said no. 'The reality is we have more people than we can take care of right now,' he told them. 'I'm sorry.… It's not what we do.' So they paid the full amount up front — $90,000 US. A trip to Moose Jaw Goodenowe offered Geoff Sando a different solution: three months living in Goodenowe's Restorative Health Centre in Moose Jaw, about 60 kilometres west of Regina, followed by a final month back in Geoff's home in Southern California. Goodenowe has converted a two-storey former drug rehab centre on the edge of town into a wellness centre for people with neurodegenerative diseases. 'It's not a fancy place. Like we call this place boot camp,' Goodenowe said as he toured CBC around the facility. 'You're not here for us to pamper you. We're here to get you out of here. Like this is rehab.' His clients, mostly ALS patients, live in dorm-like rooms and eat cafeteria-style food. Goodenowe says the program offers occasional lectures, testing services, physiotherapy and opportunities to interact with other clients. Geoff said the centre was billed as 'a place for healing' where you could 'just rest, relax, and recover.' This facility is just the beginning of Goodenowe's plans for his hometown. In April, he announced the Moose Jaw Vitality Project, which his website describes as 'a $100 million community health initiative providing free access to cutting-edge health services and monitoring technologies for all residents of Moose Jaw, Saskatchewan.' Goodenowe says this program will transform Moose Jaw into 'Canada's next 'Blue Zone' — a place where living past 100 is the norm, not the exception.' The project is planned to involve five facilities including the restorative health center, a cafe and a facility that will manufacture Goodenowe's patented plasmalogen supplements, which he has manufactured in the United States until now. 'The time has come though to incorporate these advanced technologies into routine care and into public health,' he said in a video on his website. 'Our goal is to use Moose Jaw as a beacon to the rest of the world to say 'Here's what a community who engages with each other, can actually achieve.'' Plasmalogen supplements are at the core of Goodenowe's ALS program. He says they are 'special fats' that are crucial for building cell membranes in the body — 'essential molecules for brain and heart health.' Goodenowe says people with neurological diseases like Alzheimer's, autism and ALS have a plasmalogen deficit that he can fix. 'It's basically human biochemical engineering,' he said on Dr. Amy Novotny's Reawaken Your Health Podcast late last year. 'If you actually provide the cells of the human body with the ingredients that they need and then put yourself in an environment that stimulates that adaptability, the body will fix itself.' The total cost of the four-month live-in program is $75,000 US. Geoff and Teresa were sold. 'I was really going to work hard to be the most improved,' he said. Questions emerge The couple arrived in Moose Jaw in early September 2024. It didn't take long for questions to emerge. To them, the facility didn't seem set up for people with serious degenerative diseases and mobility issues. For example, the only way to get to the second floor (where the kitchen is) is a staircase, making it inaccessible for many residents like Geoff. Goodenowe acknowledged that issue. 'We always laugh about the stairs,' Goodenowe said. 'People say, 'Dayan, when are you going to put an elevator in your facility?'' He said you can look at the stairs as part of the program. 'They'll come in not being able to walk or basically [not] being able to get out of a wheelchair. And the goal is, within three months, is to get them walking up stairs,' Goodenowe said. Teresa said that once, during an assessment, the staff left Geoff standing for too long and he fell. 'He didn't go backward or forward. He just crumpled,' she said. 'And neither of [the staff] caught him. And his legs were completely underneath him and he was screaming in pain. And they couldn't get him up.' 'That's when I became a little skeptical that, OK, they might not have the right personnel here to deal with ALS patients,' Geoff said. He said he was surprised to learn that there were no doctors or nurses on staff. Goodenowe told CBC he shouldn't have been surprised because 'we are not a medical facility. We do not provide medical care." Despite Geoff's concerns, he reminded himself that his primary reason for being there was the supplements. He still had great hope that they would work as promised. 'Self-directed research' Goodenowe provided Geoff and the other clients with a detailed day-by-day list of supplements to take at 8 a.m., noon, 4 p.m. and bedtime. The protocol includes many familiar products like creatine powder, collagen, magnesium and zinc. It also included regular doses of Goodenowe's patented plasmalogen-based products like NeuroPC+ and GliaPC+. At the bottom of the sheet, there was a footnote. 'This is a self-directed program. This protocol may be modified to suit your lifestyle and/or preferences.' In an interview with CBC, Goodenowe reiterated that point. 'We're here as a self-directed research process. People come in of their own voluntary will and they develop programs for themselves,' Goodenowe said. CBC asked Geoff about this 'self-directed research' idea. He said this was the first it had been brought to his attention and he never would have gone to Moose Jaw if he had known that was the deal. 'That's exactly the opposite of why I went to him. I went to him because he's the, supposedly, neuroscientist. I don't know anything about what to include. How am I going to self-direct?' he asked. 'You tell me this is what I need to get better, I'm going to take it.' Geoff said at no point did he develop his own program. 'The only thing I can figure out as a business person is that he's trying to limit his liability and try to claim, 'Well this is self-directed. It's not really designed by me. It's designed by the patient,'" said Geoff Timothy Caufield, the U of A law professor who specializes in legal and ethical issues in medical research, agrees. ' He wants to avoid the claim that he's providing medicine, right? That he's acting as a physician,' Caufield said. 'And his defence will be … 'I'm just providing these people with information and they're doing it themselves.'' For decades, Caufield has studied and written about what he regards as dubious medical claims. He's written academic and mainstream books like Is Gwyneth Paltrow wrong about everything? and The Cure For Everything: Untangling the Twisted Messages about Health, Fitness and Happiness. He reviewed Goodenowe's website and said he's seeing familiar patterns. 'We've studied this space for decades, and this is the go-to strategy. Heavily, heavily imply that you can cure the condition without explicitly saying you can cure the condition,' Caufield said. Caufield said if Goodenowe could really do what he's claiming, 'he should be publishing this in leading biomedical journals, having his claims and his data peer-reviewed by experts in the field, because it would be absolutely extraordinary.' He said the fact that hasn't happened is telling. 'If this individual really could do this, I promise you we would hear about it, right? This secret treatment would not be secret,' Caufield said. 'And there's no evidence that I'm aware of that would support those claims.' What's the evidence? Earlier this year, CBC asked Dayan Goodenowe for an interview about the evidence that backs up his extraordinary contention that his plasmalogen-based program can halt the progression of ALS symptoms and set patients on the path to recovery. CBC asked if he could point to any published scientific studies that back up his claim. 'Not published at this point in time,' he said. CBC asked why those studies hadn't been done. 'We're actually starting them right now,' he said. 'I'm just in negotiations with them.' Then he added that these sorts of studies are, 'not necessary for our clientele and our doctor network. This is a nutritional supplement. It's food, basically, OK? It's restoring food.' When pressed for evidence of his claims, Goodenowe points to people that seem to improve while taking his supplements. While touring the Moose Jaw facility, CBC spoke with 65-year-old Scott Myers, who had arrived from Akron, Ohio, just a few weeks earlier. 'Within the first week, I don't know if it was psychosomatic, but I had recovered the last movements that I had lost a couple weeks prior to that,' Myers said. Goodenowe also points to Corey Mitchell. In the video posted on Goodenowe's website, the 49-year-old former race car driver says, 'The disease has completely stopped. There's been no progression at all.' Goodenowe said the conclusion is clear. 'The actual progression of the disease can be stopped, OK, fundamentally unambiguously, his progression stopped,' Goodenowe said. 'It only takes one person to get better to falsify the hypothesis that this is a disease that cannot be reversed.' David Taylor, the chief scientific officer at the ALS Society of Canada, said this sort of claim is not convincing. He points out that ALS does not take a linear path. He said it's well known that patients can hit plateaus where the disease can appear to stop progressing or even improve. He adds that sometimes improvement can be attributed to placebo effects. 'It is well known that in any form of medicine, people who spend a lot of money, who go through a regimen that is more invasive, who have any kind of promises associated with a particular therapy, that those individuals do better with their disease,' Taylor said. He said he has seen no scientific evidence that plasmalogens can do what Goodenowe has claimed. 'If it were something that had a good, viable piece of information around it, we would all be looking at it. The world would go there because there'd be a lot of incentive to want to learn more about it, publish on it, make people's careers on it, and make money off of it as a pharmaceutical company,' Taylor said. 'You have an individual person's hypothesis versus an entire field of people who are spending every moment of every day trying to find that thing that's going to fix the disease.' 'You're saying Corey is a lie' Corey Mitchell's partner Jennifer Hoff said she did see improvement in his condition after he began Goodenowe's treatment program in Moose Jaw in the fall of 2023. She said his speech and ability to walk seemed to improve. She said it's possible that Goodenowe's plasmalogens helped, but also pointed out that Mitchell's stress levels dropped and his diet significantly improved while at the Moose Jaw facility. 'We changed his diet completely,' she said. 'Of course changing your diet and getting your inflammation down in your body, your body's going to respond.' Mitchell left Moose Jaw in early 2024 and his condition remained stable. Hoff said Goodenowe was clear regarding his view of Mitchell's improvement. 'He literally told him, 'You've beat ALS. You're in recovery phase. Now we just have to work on building your muscles,'' she said. In the summer of 2024, months after Mitchell shot his testimonial video, he and Hoff agreed to help Goodenowe promote the program by speaking with potential clients about the changes Mitchell had experienced. Goodenowe agreed to pay a stipend of $2,000 a month. 'We were getting bombarded with phone numbers of all these people. Hey, can you talk to so-and-so about Moose Jaw?' Hoff said. Then Mitchell's condition began to deteriorate once again. Hoff said he was no longer able to speak and so couldn't promote Goodenowe's program. Hoff reached out to Goodenowe for help. 'Not even a phone call back. And that's when I started to be like, something's not right here,' she said. Mitchell died on Oct. 21, 2024. 'What he died from wasn't from ALS progression,' Goodenowe told CBC. 'His disease did not progress to his death. He died from other causes.' When asked how he knew that, Goodenowe said, 'because he was functionally better last time I saw him. He was walking around.' Goodenowe last saw Mitchell in the summer of 2024. Hoff said Goodenowe's contention that Mitchell didn't die from ALS-related complications is 'a flat-out lie. I was there when he died. I held his hand. I watched him die.' According to Goodenowe, Mitchell's testimonial video remains on his website 'because he's still a symbol of hope, because he defied the odds.' 'His caregiver [Jennifer] said he declined and died of ALS. All of Corey's improvements, all of the work that he put through to make himself better was all bullshit, that's what you're saying to me right now,' Goodenowe said. 'You're saying Corey is a lie.' 'Sold a bill of goods' Corey Mitchell's story was instrumental in persuading Michael Giesleman to sign up for Goodenowe's ALS program. Michael died on Dec. 19, 2024, about four months after he began the program. 'He was just being sold a bill of goods and I just had to let him,' his wife Shannon said. 'That's how he chose to spend his last days.' She said she watched Michael become a different person after learning of his diagnosis. She said the desperation to find a cure consumed him. 'It took away his whole spirit. It took away everything,' she said. 'ALS is a no-win situation. The best thing you can do is just accept it and be happy right now and just live your life right now.' Geoff Sando is now back in California. His condition has deteriorated. 'Really didn't experience any halting of the progression while I was there or anytime since,' Geoff said. 'Actually it seemed like it was picking up pace, not slowing down." He added that he became friends with several through the program and they have stayed in touch. 'And it wasn't just me," he said. 'Everybody had declined pretty significantly.' Becky Bader is one of them. She was diagnosed with ALS in April 2024 and began attending Goodenowe's Moose Jaw program in early September — one day before Geoff and Teresa arrived. According to her husband Eric, she was losing about a point a month on the 48-point ALS functional rating scale, a questionnaire that helps to keep track of a patient's decline in speech, movement and breathing. Then she began Goodenowe's program. 'She lost two points the first month, two points the second month, three points the third month,' said Eric, who attended the program with her. 'So her functionality decrease accelerated.' Eric said he knows the disease is not linear, so he doesn't attribute her worsening condition to Goodenowe's treatment. However, 'we definitely did not see any improvement… Absolutely not.' Becky died last month — May 18, 2025. When CBC pointed out to Goodenowe that some of his clients said they had declined while on his program, he expressed doubt. 'So how documented is that decline? Do they have evidence of their decline or is it just their opinion?' he asked. 'We do document every single person that comes through our centre, OK? They leave that centre better than they came in, OK? And that's just simply a fact, OK?' Health Canada steps in Geoff and Teresa wonder how a facility like this is allowed to operate in Canada. They have filed complaints with Saskatchewan's College of Physicians and Surgeons and the Moose Jaw Police Service. They don't know where else to turn. Timothy Caufield said this story highlights a real problem. Goodenowe is not a medical doctor, so he's not under the jurisdiction of the College of Physicians and Surgeons. 'We need as a society to be able to transparently and appropriately stop individuals like this from doing what I think is clear and real harm,' Caufield said. 'The fact that we can't easily do it is really problematic.' Some action has been taken. In January, Health Canada began investigating Goodenowe's company. 'Following an onsite inspection on March 20, 2025, Health Canada found the company was importing, advertising, and selling unauthorized natural health products,' Health Canada said in a statement. All natural health products must be assessed by the government for safety before they can be legally sold in Canada. Health Canada says that since the inspection, 'the company confirmed they had stopped importing and selling unauthorized NHPs. They also committed to not promoting unauthorized health products and corrected their website.' Goodenowe said Health Canada's concerns were based on a misunderstanding. He said individual clients are able to import up to a 90-day supply of the plasmalogen supplements for personal use. He said some of those supplements had, instead, been shipped to his Moose Jaw company. 'What that meant was, we had accepted shipment on behalf of a client that wasn't directly labelled,' Goodenowe said. 'The Health Canada inspector said, 'Hey, you need to make sure that these things are properly labelled for the client that's receiving them,' and we said, 'Thank you, we'll fix that.'" Hopes dashed Geoff Sando is now spending as much time as he can with his family. His adult children live in his house and help with his care. When he started this process, he had visions of coming home to a hero's welcome. 'I thought I was going to come home and walk up those stairs from my garage in here,' he said. He justified the expense and the time away from family as an investment. 'Instead of two years with my kids, I would have 15, 20 years with my kids,' he said. 'Get to see my grandchildren. Be able to walk my daughter down the aisle. I don't know if I'll get to do any…' He trailed off, overtaken by emotion. Geoff said maybe Goodenowe has the nugget of a promising idea, but 'he hasn't developed something that stops progression in ALS… he's at best trying to figure it out.' 'We are part of an experiment. And that's not what I signed up to be and paid him a lot of money for — to be part of a trial.' About the Author Footer Links My Account Profile CBC Gem Newsletters Connect with CBC Facebook Twitter YouTube Instagram Mobile RSS Podcasts Contact CBC Submit Feedback Help Centre Audience Relations, CBC P.O. Box 500 Station A Toronto, ON Canada, M5W 1E6 Toll-free (Canada only): 1-866-306-4636 TTY/Teletype writer: 1-866-220-6045 About CBC Corporate Info Sitemap Reuse & Permission Terms of Use Privacy Jobs Our Unions Independent Producers Political Ads Registry AdChoices Services Ombudsman Public Appearances Commercial Services CBC Shop Doing Business with Us Renting Facilities Accessibility It is a priority for CBC to create a website that is accessible to all Canadians including people with visual, hearing, motor and cognitive challenges. Closed Captioning and Described Video is available for many CBC shows offered on CBC Gem. About CBC Accessibility Accessibility Feedback © 2025 CBC/Radio-Canada. All rights reserved. Visitez
CTV News
an hour ago
- CTV News
Clinton emergency department closing for part of the weekend
Clinton Public Hospital as seen in August 2021. (Source: Huron Perth Healthcare Alliance) Officials with the Huron Perth Healthcare Alliance (HPHA) say due to ongoing staff shortages, the emergency department (ED) at the Clinton Public hospital will run on reduced hours this weekend. The ED will close at 8 p.m. Friday, and it won't reopen until 8 a.m. Sunday. Anyone requiring immediate medical attention should contact 911. First responders will transport you to the nearest available ED. The closest hospitals to Clinton include the Seaforth Community Hospital, Goderich's Alexandra Marine and General Hospital, and Exeter's South Huron Hospital.
