Podcasts about Beaton

The PLZ panel have sympathy for John Beaton as the ref for Sunday's 'Old Firm' fixture. The race for the title. VAR revamp. The problems at 'New Firm'. Just a few of the topics discussed on the Journos, as well as the search for the Hibs fan who apparently wants Hearts to win the League!

The Go Radio Football Show: 24th of February 2026. PLAY and HIT SUBSCRIBE, and NEVER miss an episode! A weekend where controversy overshadowed quality, tempers flared on and off the pitch, and the title race somehow became even tighter. This episode is a full‑throttle dive into the most controversial refereeing weekend of the season — and the decision to hand John Beaton the whistle for Rangers v Celtic. With VAR dominating headlines, Paul Cooney, Mark Guidi and Darren O'Dea unpack a catalogue of officiating errors, the psychology of referees under scrutiny, and the growing sense that the title race is being shaped as much by the men in the middle as the players on the pitch. The Beaton Appointment Shock Darren O'Dea admits he's “surprised he's been picked” for the derby. Mark Guidi goes harder: Beaton's “off‑form this season” and hasn't earned this fixture. The panel question whether Willie Collum has chosen form — or simply rotation. VAR: From Safety Net to Circus Multiple examples of VAR interventions that still produced the wrong outcome. Mark blasts the “cosiness” between refs and VAR officials — no one wants to overrule a colleague. Darren: the real anger comes from refs having all the angles… and still getting it wrong. The Trusty Red Card & Scales Penalty Debate O'Dea: Trusty's action was “idiotic” but not the kind of thing you want to see red cards for. Guidi: Scales' jersey pull happens at every set piece — not a penalty for him. Celtic's appeal? Dismissed. Three‑match ban stands. Rangers' Stumble at Livingston Danny Röhl praises the “character” to come back from 2–0 down. Fans furious at dropped points against a side winless since August. Caller Paul questions John Souttar's form — and whether he's costing Rangers. Hearts & Motherwell: The Real Title Disruptors Hearts keep grinding out results; Guidi says they're “playing with no pressure.” Motherwell's defensive record is elite — only 18 conceded in 27 games. Caller Hugh claims they could go unbeaten in the final 11 games. Darren doesn't dismiss it. Celtic's Form Crisis O'Dea: Celtic “don't look like Celtic” and will need to scrap their way through the run‑in. Guidi: despite everything, the title is still in Celtic's hands — win out, and they're champions. The Old Firm Showdown Looms Rangers favourites at Ibrox — but neither side convincing. Guidi: Rangers haven't won a meaningful derby in years. O'Dea: the winner on Sunday gets the psychological spark they've both been missing. Follow us @thisisgoradio on Instagram, Facebook, LinkedIn and Tik Tok The Go Radio Football Show, weeknights from 5pm-7pm across Scotland on DAB, YouTube, Smart Speaker - launch Go Radio - and on the Go Radio App. IOS: https://apps.apple.com/gb/app/go-radio/id1510971202 Android: https://play.google.com/store/apps/details?id=uk.co.thisisgo.goradio&pcampaignid=web_share In Association with Burger King. Home of the Whopper, home delivery half time or full time, exclusively on the Burger King App  https://www.burgerking.co.uk/download-bk-app. Watch the Replay on YouTube: https://www.youtube.com/live/PdDgYNnDw7I?si=g8XsmaQp4qWAqaYx   For more Podcasts from Go Studios, head to: https://thisisgo.co.uk/podcasts/ Facebook: https://www.facebook.com/share/1ATeQD... 

Hi! My name is Terry J. Aman, marking my 107th episode of VideoFuzzy titled "Persons Unknown," reporting the progress I've made in cataloging thousands of VHS transfers and digital recordings. "Persons Unknown" was a short-run summer series in 2010 on NBC, archived across now three binders in my collection, including an episode that never aired, archived to my current collection, as well as a home-burned disc set I crafted while watching them for this feature, which has also been posted to VideoFuzzy's YouTube channel as my 15th ever VideoFuzzy the Video: https://youtu.be/X0j2mMfjFng In Cross Connections, I track connections through the cast of "Persons Unknown" as well as Barry Bostwick, Chi McBride, Aldis Hodge, Chris Gaultier, Colin Mochrie, Danny Strong, John Billingsley, Erik Charles Nielsen and Charissa Barton. Under Fond Reflection, I celebrate the life and work of Catherine O'Hara as a Golden Thread in my collection. In my Classic Collection [VHS-to-DVD transfers], this set covered discs 1951-1975. An extension of strange coincidence I outlined last time, this was just the craziest set of circumstances, a search for a couple of ads that turned up in my collection came up empty so they ended up on VideoFuzzy's Instagram. That search, however, did turn up the final two episodes of "Strange Luck," a mid-'90s FOX production, these two on the YouTube channel @OASMovies-gw5tz and also posted within the past year. Wild! Also, Isabella Rossellini explored the sex lives of bedbugs on the Sundance channel, which showed up as a clip and some commentary on "The Daily Show with Jon Stewart," a staticky copy of "The Rocky Horror Picture Show," and Jensen Ackles lip-syncing to Survivor's "Eye of the Tiger" in the credit sequence for a fourth-season episode of "Supernatural." https://bit.ly/3MkLSmd In my Current Collection [direct to digital], I added the two episodes of "Strange Luck" that I found, along with a classic production of Agatha Christie's "The Seven Dials Mystery" from 1981 on AcornTV as well as the three-part Netflix adaptation. Also, comments on "Wake Up Dead Man: A Knives Out Mystery," issues with tubi's production of "Doctor Who," and Jack Smith's testimony to the House Judiciary Committee and comments from there. In Book Reports, I've been walking a lot more and reading a lot of authors through my audible account. I've read three by Sophie Hannah, a short story collection by Agatha Christie and one each by Riley Sager, Marthe Jocelyn, Maureen Johnson and this one I'll recommend highly, "Agatha Raisin and the Quiche of Death" by M.C. Beaton, which was absolutely delightful. Finally, in What I've Been Watching, my husband, Ralph, and I just finished watching "My Hero Academia," I've encountered a few episodes of "Miss Fisher's Murder Mysteries," and over new year's I took in "Marty Supreme." Fun! SPREADING THE WORD! "VideoFuzzy: The Video - Celebrating 100 Episodes!" is posted at https://youtu.be/eWfcCDiOZ2I. Please share as you're able to with anyone you feel might enjoy this production. For PROMOS, scroll all the way down at https://videofuzzy.libsyn.com. Also, there's a "Top Fifteen" episode guide for people looking for a quick read-in on this blog and podcast effort at: https://videofuzzy.libsyn.com/about. Enjoy!

In this special episode, recorded live at the 2025 Genomics England Research Summit, host Adam Clatworthy is joined by parents, clinicians and researchers to explore the long, uncertain and often emotional journey to a genetic diagnosis. Together, they go behind the science to share what it means to live with uncertainty, how results like variants of uncertain significance (VUS) are experienced by families, and why communication and support matter just as much as genomic testing and research. The panel discuss the challenges families face when a diagnosis remains out of reach, the role of research in refining and revisiting results over time, and how collaboration between researchers, clinicians and participants could help shorten diagnostic journeys in the future. Joining Adam Clatworthy, Vice-Chair for the Participant Panel, on this episode are: Emma Baple – Clinical geneticist and Medical Director, South West Genomic Laboratory Hub  Jamie Ellingford – Lead genomic data scientist, Genomics England  Jo Wright – Member of the Participant Panel and Parent Representative for SWAN UK  Lisa Beaton - Member of the Participant Panel and Parent Representative for SWAN UK  Linked below are the episodes mentioned in the episode:  What is the diagnostic odyssey?  What is a Variant of Uncertain Significance?  Visit the Genomics England Research Summit website, to get your ticket to this years event. You can download the transcript, or read it below. Sharon: Hello, and welcome to Behind the Genes. My name is Sharon Jones and today we're bringing you a special episode recorded live from our Research Summit held in June this year. The episode features a panel conversation hosted by Adam Clatworthy, Vice-Chair of the Participant Panel. Our guests explore navigating the diagnostic odyssey, the often-complex journey to reaching a genetic diagnosis. If you'd like to know more about what the diagnostic odyssey is, check our bitesize explainer episode, ‘What is the Diagnostic Odyssey?' linked in the episode description. In today's episode you may hear our guests refer to ‘VUS' which stands for a variant of uncertain significance. This is when a genetic variant is identified, but its precise impact is not yet known. You can learn more about these in another one of our explainer episodes, “What is a Variant of Uncertain Significance?” And now over to Adam. -- Adam: Welcome, everyone, thanks for joining this session. I'm always really humbled by the lived experiences and the journeys behind the stories that we talk about at these conferences, so I'm really delighted to be hosting this panel session. It's taking us behind the science, it's really focusing on the people behind the data and the lived experiences of all the individuals and the families who are really navigating this system, trying to find answers and really aiming to get a diagnosis – that has to be the end goal. We know it's not the silver bullet, but it has to be the goal so that everyone can get that diagnosis and get that clarity and what this means for their medical care moving forwards.    So, today we're really going to aim to demystify what this diagnostic odyssey is, challenging the way researchers and clinicians often discuss long diagnostic journeys, and we'll really talk about the vital importance of research in improving diagnoses, discussing the challenges that limit the impact of emerging research for families on this odyssey and the opportunities for progress. So, we've got an amazing panel here. Rather than me trying to introduce you, I think it's great if you could just introduce yourselves, and Lisa, I'll start with you. Lisa: Hi, I'm Lisa Beaton and I am the parent of a child with an unknown, thought to be neuromuscular, disease. I joined the patient Participant Panel 2 years ago now and I'm also a Parent Representative for SWAN UK, which stands of Syndromes Without A Name. I have 4 children who have all come with unique and wonderful bits and pieces, but it's our daughter who's the most complicated. Adam:  Thank you. Over to you, Jo. Jo:  Hi, I'm Jo Wright, I am the parent of a child with an undiagnosed genetic condition.  So I've got an 11-year-old daughter. 100,000 Genomes gave us a VUS, which we're still trying to find the research for and sort of what I'll talk about in a bit.  And I've also got a younger daughter. I joined the Participant Panel just back in December. I'm also a Parent Rep for SWAN UK, so Lisa and I have known each other for quite a while through that. Adam:  Thank you, Jo.  And, Jamie, you're going to be covering both the research and the clinician side and you kind of wear 2 hats, so, yeah, over to you. Jamie:  Hi, everyone, so I'm Jamie Ellingford and, as Adam alluded to, I'm fortunate and I get to wear 2 hats. So, one of those hats is that I'm Lead Genomic Data Scientist for Rare Disease at Genomics England and so work as part of a really talented team of scientists and engineers to help develop our bioinformatic pipelines, so computational processes. I work as part of a team of scientists and software engineers to develop the computation pipelines that we apply at Genomics England as part of the National Health Service, so the Genomic Medicine Service that families get referred to and recruited to, and we try to develop and improve those. So that's one of my hats. And the second of those is I am a researcher, I'm an academic at the University of Manchester, and there I work really closely with some of the clinical teams in the North West to try and understand a little bit more about the functional impact of genomic variants on kind of how things happen in a cell. So, we can explore a little bit more about that but essentially, it's to provide a little bit more colour as to the impact that that genomic variant is having. Adam: Great, thank you, Jamie. Over to you, Emma. Emma: My name's Emma Baple, I'm an academic clinical geneticist in Exeter but I'm also the Medical Director of the South West genomic laboratory hub, so that's the Exeter and Bristol Genomics Laboratory. And I wear several other hats, including helping NHS England as the National Specialty Advisor for Genomics. Adam: Thank you all for being here. I think it's really important before we get into the questions just to ground ourselves in like those lived experiences that yourself and Jo and going through. So, Lisa, I'm going to start with you. The term ‘diagnostic odyssey' gets bandied around a lot, we hear about it so many times, but how does that reflect your experience that you've been through and what would you like researchers and clinicians to understand about this journey that you're on, essentially? Lisa: So I think ours is less an odyssey and more of a roller-coaster, and I say that because we sort of first started on a genetic journey, as it were, when my daughter was 9 weeks of age and she's now 16½ – the half's very important – and we still have no answers. And we've sort of come a bit backwards to this because when she was 6 months old Great Ormond Street Hospital felt very strongly that they knew exactly what was wrong with her and it was just a case of kind of confirmation by genetics. And then they sent off for a lot of different myasthenia panel genes, all of which came back negative, and so having been told, “Yes, it's definitely a myasthenia, we just need to know which one it is,” at 4 years of age that was removed and it was all of a sudden like, “Yeah, thanks, sorry.” And that was really hard actually because we felt we'd had somewhere to hang our hat and a cohort of people with very similar issues with their children, and then all of a sudden we were told, “No, no, that's not where you belong” and that was a really isolating experience. I can remember sort of saying to the neuromuscular team, “Well is it still neuromuscular in that case?” and there was a lot of shrugging of shoulders, and it just…  We felt like not only had we only just got on board the life raft, then we'd been chucked out, and we didn't even have a floaty. And in many ways I think I have made peace with the fact that we don't have a genetic diagnosis for our daughter but it doesn't get easier in that she has her own questions and my older children – one getting married in August who's already sort of said to me, you know, “Does this have implications for when we have children?”  And those are all questions I can't answer so that's really hard. Adam:  Thank you, Lisa. Yourself, Jo, how would you describe the odyssey that you're currently experiencing? Jo: So my daughter was about one when I started really noticing that she was having regressions. They were kind of there beforehand but, I really noticed them when she was one, and that's when I went to the GP and then got referred to the paediatrician. So initially we had genetic tests for things like Rett syndrome and Angelman syndrome, which they were all negative, and then we got referred on to the tertiary hospital and then went into 100,000 Genomes. So we enrolled in 100,000 Genomes at the beginning of 2017, and we got our results in April of 2020, so obviously that was quite a fraught time. Getting our results was probably not as you would want to do it because it was kind of over the phone and then a random letter. So, what I was told in that letter was that a variant of uncertain significance had been identified and they wanted to do further research to see if it might be more significant. So we were to be enrolled into another research project called Splicing and Disease, which wasn't active at the time because everything had been put on hold for COVID, but eventually we went into that. So, I didn't know what the gene was at that point, when I eventually got the form for going to get her bloods done…  So that went off and then that came back and the geneticist said, “That gives us some indication that it is significant.” So, since that point it's been trying to find more information and research to be able to make it a diagnosis. There have been 2 sort of key things that have happened towards that but we're still not there. So one of the things is that a research paper came out earlier this year so that's kind of a little bit more evidence, it's not going to give us a diagnosis but it kind of, you know, sits there. And the other thing is that my geneticist said, “Actually, yeah, it looks like it's an important change.”  That's as far as we've got. So we've still got work to do to make it a diagnosis or not.  Obviously if it is a diagnosis, it is still a one-of-a-kind diagnosis, so it doesn't give me a group to join or that kind of thing. But now I've got that research paper that I've read and read, and asked ChatGPT to verify that I've understood it right in some places, you know, with the faith that we put into ChatGPT (laughs), I've got a better understanding and I've got something now that I can look back on, the things that happened when my daughter was one, 2, 3, 4 and her development was all over the place and people thought that I was slightly crazy for the things I was saying, that “Actually, no, I can see what's happening.” So, it's like the picture's starting to come into focus but there's work to do. I haven't got a timeframe on that, I don't know when it's going to come together. And I always say that I'm a prolific stalker of the postman; ever since our first genetic tests you're just constantly waiting for the letters to drop through the door. So a diagnostic odyssey to me is just waiting for random events. Adam: I think what you've both kind of really clearly elaborated on is how you're the ones that are having to navigate this journey, you're the ones that are trying to piece this puzzle together, and the amount of time you're investing, all whilst navigating and looking after your child and trying to cope with the daily lived experience as well. And something you've both touched on that I'd love to draw out more is about how exactly was the information shared with you about the lack of diagnosis or the VUS or what's going on, because in our case you get this bit of paper through the post that has all these numbers and it's written in clinical speak and we had no conversation with the geneticist or the doctors. You see this bit of paper and you're reading it, scared for what the future will hold for your child, but I'd love to know like how were you communicated whilst all this is going on, how did you actually find out the next steps or any kind of future guidance. Lisa: So I think in our case we kept sort of going onto neuromuscular appointments, and I think for probably the first 5 years of my daughter's life I kind of had this very naïve thought that every time we turned up to an appointment it would be ‘the one' and then…   I think it would've been really helpful actually in those initial stages if they had said to us, “Actually, we don't know when this is going to happen, if it's even going to happen, you need to kind of prepare yourself for that.” It sounds fairly obvious to say but you don't know what you don't know. And in some ways we were getting genetic test results back for some really quite horrible things and they would tell us, “Oh it's good news, this mitochondrial disorder hasn't come up,” and so part of you is like, “Yay!” but then another part of you is thinking, “Well if it's not that what is it?” And we've very much kind of danced around and still don't really have an answer to whether it's life-limiting. We know it's potentially life-threatening and we have certain protocols, but even that is tricky. We live in North Yorkshire, and our local hospital are amazing. Every time we go in, if it's anything gastro-related, they say to me, “What's the protocol from Great Ormond Street?” and I say, “We don't have one” (laughs) and that always causes some fun. We try to stay out of hospitals as much as we absolutely can and do what we can at home but, equally, there's a point where, you know, we have to be guided by where we're going with her, with the path, and lots of phone calls backwards and forwards, and then is it going to be a transfer down to Great Ormond Street to manage it. And actually the way I found out that nothing had been found from 100,000 Genomes was in a passing conversation when we had been transferred down to Great Ormond Street and we'd been an inpatient for about 6 weeks and the geneticist said to me, “So obviously with you not having a diagnosis from the 100,000 Genomes…” and I said, “Sorry?  Sorry, what was that?  You've had the information back?”  And she said, “Well, yes, did nobody write to you?” and I said, “No, and clearly by my shock and surprise.” And she was a bit taken aback by that, but it happened yet again 2 years later (laughs) when she said, “Well you know everything's been reanalysed” and I said, “No.”  (Laughs)  And, so that's very much, it still feels an awful lot like I'm doing the heavy lifting because we're under lots of different teams and even when they're working at the same hospital they don't talk to each other. And I do understand that they're specialists within their own right, but nobody is really looking at my daughter holistically, and there are things that kind of interrelate across.    And at one of the talks I attended this morning they were talking about the importance of quality of life, and I think that is something that has to be so much more focused on because it's hard enough living without a diagnosis, but when you're living with a bunch of symptoms that, I think the best way I can describe it is at the moment we've got the spokes of the umbrella but we don't have the wrapper, and we don't know where we're going with it. We can't answer her questions, we can't even necessarily know that we're using the most effective treatments and therapies for her, and she's frustrated by that now, being 16, in her own right, as well as we are. And I'm panicking about the navigation towards Adult Services as well because at the minute at least we have a clinical lead in our amazing local paediatrician but of course once we hit and move into that we won't even have him and that's a really scary place to be, I think. Adam: Jo, is there anything you wanted to add on that in terms of how you've been communicated to whilst all this is going on? Jo: Yeah, so I think part of what makes it difficult is if you're across different hospitals because they're not necessarily going to see the same information. So obviously it was a bit of a different time when I got our results, but I got our results on a virtual appointment with a neurologist in one hospital, in the tertiary hospital, and because he could see the screen because it was the same hospital as genetics, and he said, “Oh you've got this” and then the letter came through later. When I had my next appointment with the neurologist in our primary hospital, or secondary care, whatever it's called, in that hospital, he hadn't seen that, so I'm telling him the results, which isn't ideal, but it happens quite a lot. What I think is quite significant to me is the reaction to that VUS.  I have to give it, the doctors that look after my daughter are brilliant, and I'm not criticising them in any way but their reaction to a VUS is “I'm so grateful for the persistence to get to a diagnosis.” Neurologists are a bit more like “Oh it's a VUS so it might be significant, it might be nothing.” Actually, as a patient, as in a parent, you actually want to know is it significant or not, “Do I look at it or not?” And, I mean, like I said, there were no research papers to look at before anyway until a few months ago so I didn't have anything to look at, but I didn't want to look at it either because you don't want to send yourself off down a path. But I think that collective sort of idea that once someone gets a VUS we need a pathway for it, “What do we do with it, what expectation do we set the patients up with and what is the pathway for actually researching further?” because this is where we really need the research. Adam:  Thank you, Jo. So, Emma, over to you in terms of how best do you think clinicians can actually support patients at navigating this odyssey and what's the difference between an initial diagnosis and a final diagnosis and how do you then communicate that effectively to the patients and their family?   Emma: So I think a key thing for me, and it's come up just now again, is that you need to remember as a doctor that the things you say at critical times in a patient's or parent's journeys they will remember – they'll remember it word for word even though you won't – and thinking about how to do that in the most sensitive, empathetic, calm, not rushed way is absolutely key.   And there are some difficulties with that when you're in a very high-pressure environment but it is absolutely crucial, that when you are communicating information about test results, when you're talking about doing the test in the first place, you're consenting the family, you're explaining what you're trying to do and those conditions, you balance how much information you give people.    So, you were talking earlier about “So you haven't got this diagnosis, you haven't got that diagnosis,” I often think it's…  We're often testing for numerous different conditions at the same time, I couldn't even list them all to the parents of the children or the patient that I'm testing. It's key to try and provide enough information without overwhelming people with so much information and information on specific conditions you are just thinking about as a potential.  Sometimes very low down your list actually but you can test for them.    Because people go home and they use the internet and they look things up and they get very, very worried about things. So, for me it's trying to provide bite-sized amounts of information, give it the time it deserves, and support people through that journey, tell them honestly what you think the chance of finding a diagnosis is. If you think it's unlikely or you think you know, sharing that information with family is helpful.   Around uncertainty, I find that a particular challenge. So, I think we've moved from a time when we used to, in this country, declare every variant we identified with an uncertain significance. Now, if we remember that we've all got 5 million variants in our genome, we've all got hundreds and hundreds… thousands and thousands, in fact, of variants of uncertain significance in our genetic code. And actually, unless you think a variant of uncertain significance genuinely does have a probability of being the cause of a child's or a patient's condition, sharing that information can be quite harmful to people.    We did a really interesting survey once when we were writing the guidelines for reporting variants of uncertain significance a few years ago. We asked the laboratories about their view of variants of uncertain significance and we asked the clinicians, and the scientists said, “We report variants of uncertain significance because the clinicians want them” and the clinicians said, “If the labs put the variant of uncertain significance on the report it must be important.” And of course, if you're a parent, if the doctor's told you the variant is a variant of uncertain significance of course you think it's important.    So, we should only be sharing that information, in my opinion, if it genuinely does have a high likelihood of being important and there are things that we can do. And taking people through that journey with you, with the degree of likelihood, the additional tests you need to do and explaining to them whether or not you think you will ever clarify that, is really, really key because it's very often that they become the diagnosis for the family.  Did I cover everything you think's important, both of you?  Lisa: I think the one thing I would say is that when you are patient- or parent-facing, the first time that you deliver that news to the parent… you may have delivered that piece of news multiple times and none of us sit there expecting you to kind of be overcome with emotion or anything like that but, in the same way that perhaps you would've had some nerves when, particularly if it was a diagnosis of something that was unpleasant, you know, to hold onto that kind of humanity and humility. Because for those patients and parents hearing that news, that is the only time they're ever hearing that, and the impact of that, and also, they're going on about with their day, you don't know what else they're doing, what they're juggling.    We're not asking you all to be responsible for kind of, you know, parcelling us up and whatnot but the way information is imparted to us is literally that thing we are all hanging our hats on, and when we're in this kind of uncertainty, from my personal experience I'm uncomfortable, I like to be able to plan, I'm a planner, I'm a researcher, I like to sort of look it up to the nth degree and that, and sitting in a place without any of that is, it's quite a difficult place to be. And it's not necessarily good news for those parents when a test comes back negative, because if it's not that then what is it, and that also leaves you feeling floundering and very isolated at times.  Adam: Yeah, and you touched upon the danger of like giving too much information or pushing families down a particular route, and then you have to pull them out of it when it's not that.   You talked about the experience you had, you felt like you'd found your home and then it's like, “Well, no, no, sorry, actually we don't think it's that.” And you've invested all of your time and your emotion into being part of that group and then you're kind of taken away again. So it's to the point where you have to be really sure before you then communicate to the families, and obviously in the meantime the families are like, “We just need to know something, we need to know,” and it's that real fine line, isn't it?    But, Jamie, over to you. Just thinking about the evolving nature of genomic diagnosis, what role does research play in refining or confirming a diagnosis over time?  Jamie: So it's really, really difficult actually to be able to kind of pinpoint one or 2 things that we could do as a community of researchers to help that journey, but perhaps I could reflect on a couple of things that I've seen happen over time which we think will improve things. And one of that's going back to the discussion that we've just had about how we classify genetic variants. And so, behind that kind of variant of uncertain significance there is a huge amount of effort and emotion from a scientist's side as well because I think many of the scientists, if not all, realise what impact that's going to have on the families.   And what we've tried to do as a community is to make sure that we are reproducible, and if you were to have your data analysed in the North West of England versus the South West that actually you'd come out with the same answer. And in order to do that we need guidance, we need recommendations, we need things that assist the scientists to actually classify those variants.  And so, what we have at the moment is a 5 point scale which ranges from benign to likely benign, variant of uncertain significance, unlikely pathogenic variant and pathogenic variant. It's objective as to how we classify a variant into one of those groups and so it's not just a gut feeling from a scientist, it's kind of recordable measurable evidence that they can provide to assist that classification.   So in many instances what that does is provide some uncertainty, as we've just heard, because it falls into that zone of variant of uncertain significance but what that also does is provide a framework in which we can generate more evidence to be able to classify it in one direction or another to become likely pathogenic or to become likely benign. And as a research community we're equipped with that understanding –– and not always with the tools but that's a developing area – to be able to do more about it.   What that doesn't mean is that if we generate that evidence that it can translate back into the clinic, and actually that's perhaps an area that we should discuss more. But kind of just generating that evidence isn't always enough and being able to have those routes to be able to translate back that into the hands of the clinicians, the clinical scientists, etc, is another challenge. Adam:  And how do you think we can drive progress in research to deliver these answers faster, to really try and shorten those diagnostic journeys, like what are the recommendations that you would say there? Jamie:  So being able to use the Genomics England data that's in the National Genomic Reference Library, as well as kind of other resources, has really transformed what we can do as researchers because it enables teams across the UK, across the world to work with data that otherwise they wouldn't be able to work with.   Behind that there's an infrastructure where if researchers find something which they think is of interest that can be reported back, it can be curated and analysed by teams at Genomics England and, where appropriate, kind of transferred to the clinical teams that have referred that family. And so having that pathway is great but there's still more that we can do about this. You know, it's reliant on things going through a very kind of fixed system and making sure that clinicians don't lose contact with families – you know, people move, they move locations, etc. And so, I think a lot of it is logistical and making sure that the right information can get to the right people, but it all falls under this kind of umbrella of being able to translate those research findings, where appropriate, into clinical reporting.   Adam:  Thank you. And, Emma, is there anything you would add in terms of like any key challenges that you think need to be overcome just to try and shorten the journeys as much as possible and find the answers to get a diagnosis?  Emma: I think trying to bridge that gap between some of the new technologies and new approaches that we've got that we can access in a research context and bringing those into diagnostics is a key area to try to reduce that diagnostic odyssey, so I really want to see the NHS continuing to support those sorts of initiatives.   We're very lucky, as Jamie said, the National Genomic Research Library has been fundamental for being able to reduce the diagnostic odyssey for large numbers of patients, not just in this country but around the world, and so trying to kind of look at how we might add additional data into the NGRL, use other research opportunities that we have in a more synergistic way with diagnostics I think is probably key to being able to do that.    We are very lucky in this country with the infrastructure that we've got and the fact that everything is so joined up. We're able to provide different opportunities in genomics for patients with rare conditions that aren't so available elsewhere in the world.  Adam: Great, thank you. I think we're it for time, so thank you very much to the panel. And I'd just say that if you do have any further questions for ourselves as participants then we're only too happy to pick those up. Thank you for lasting with us ‘til the end of the day and hope to see you soon.  -- Sharon: A huge thank you to our panel, Adam Clatworthy, Emma Baple, Jo Wright, Lisa Beaton and Jamie Ellingford, for sharing their insights and experiences. Each year at the summit, the Behind the Genes stage hosts podcast style conversations, bringing together researchers, clinicians and participants to discuss key topics in genomics.  If you're interested in attending a future Genomics England Research Summit, keep an eye out on our socials. If you'd like to hear more conversations like this, please like and subscribe to Behind the Genes on your favourite podcast app. Thank you for listening.    I've been your host, Sharon Jones. The podcast was edited by Bill Griffin at Ventoux Digital and produced by Deanna Barac.

Protect your family with our 1-minute free parent quiz https://www.smartsocial.com/newsletterJoin our next weekly live parent events:  https://smartsocial.com/eventsEpisode Summary:In this episode of the SmartSocial.com Podcast, host Josh Ochs sits down with Andy Beaton, Assistant Superintendent in ISD 622, to discuss the challenges and strategies for keeping students safe online. The conversation covers a range of topics including the implications of AI on student learning, the dangers of social media, and the importance of digital citizenship. With valuable tips for parents, educators, and administrators, Andy shares his extensive experience and insights on how to foster a safe and productive digital environment for young people.Become a Smart Social VIP (Very Informed Parents) Member: https://SmartSocial.com/vipDistrict Leaders: Schedule a free phone consultation to get ideas on how to protect your students in your community https://smartsocial.com/partnerDownload the free Smart Social app: https://www.smartsocial.com/appdownloadLearn about the top 190+ popular teen apps: https://smartsocial.com/app-guide-parents-teachers/View the top parental control software: https://smartsocial.com/parental-control-software/The SmartSocial.com Podcast helps parents and educators to keep their kids safe on social media, so they can Shine Online™

Higher education is shifting toward a connected model where colleges and universities function as one learner ecosystem. The goal is simple: make credentials stackable, transfer predictable, and pathways flexible enough for learners to move in and out of education as their careers evolve.In this episode of The TechEd Podcast, Matt Kirchner speaks with Dr. Katherine Frank (Chancellor, University of Wisconsin–Stout) and Dr. Sunem Beaton-Garcia (President, Chippewa Valley Technical College) about how their institutions have developed streamlined pathways for learners that support lifelong learning.They break down how institutions can design on-ramps and off-ramps, align programs across tech/community college and university systems, expand credit recognition, and keep partnerships active so transfer works in real life (no more "credits to nowhere"). The conversation also expands to what this shift means nationally as technology and workforce needs change faster.In this episode:What a connected model for colleges and universities actually requires in program design and policyHow to make transfer predictable and student-friendly without lowering academic standardsWhy stackable credentials and credit for prior learning matter more as learners move in and out of educationHow to get around the red tape that has traditionally prevented colleges and universities from creating streamlined transfer pathwaysWhat higher education leaders should do next if they want to build the new model in their own region3 Big Takeaways from this Episode:1. A connected model keeps learners moving across colleges and universities. Stackable credentials, credit for prior learning, and predictable transfer reduce the stop-and-start pattern that derails working adults and career-changers. When pathways are designed for entry, exit, and return, education becomes a long-term system learners can use throughout their careers.2. Transfer works at scale when it becomes an operating habit, not a one-time agreement. The UW–Stout and CVTC alignment shows what changes when institutions treat pathway design as ongoing work with shared ownership and recurring check-ins. That consistency is what makes transfer feel clear to students and sustainable for faculty and staff.3. This model makes it easier to keep programs aligned as technology and jobs change. Modular, competency-aligned pathways let institutions update portions of a program without rebuilding the entire structure. It is a practical way to respond faster to industry signal while protecting rigor and program quality.Resources in this Episode:Read the op-ed co-written by Drs. Frank and Beaton-Garcia: "Reframing Higher Education"➡️ Find more resources on the episode page: https://techedpodcast.com/disruption/We want to hear from you! Send us a text.Instagram - Facebook - YouTube - TikTok - Twitter - LinkedIn

In this episode of the podcast, recorded just before he took office, we speak with the 2026 CII President Callum Beaton FCII. We discuss his theme for his presidential year, his experience and hopes for the future of the profession.

In this video we cover Rheumatic Fever; What is it? Rheumatic Fever Pathophysiology, the signs and symptoms of rheumatic fever as well as the diagnosis of rheumatic fever (including the Jones criteria and a rheumatic fever mnemonic!). We then look at the treatment. PDFs available here: https://rhesusmedicine.com/pages/rheumatologyConsider subscribing (if you found any of the info useful!): https://www.youtube.com/channel/UCRks8wB6vgz0E7buP0L_5RQ?sub_confirmation=1Buy Us A Coffee!: https://www.buymeacoffee.com/rhesusmedicineVideo Timestamps:0:00 What is Rheumatic Fever? 0:30 Rheumatic Fever Pathophysiology1:53 Rheumatic Fever Symptoms / Signs and Symptoms of Rheumatic Fever3:46 Jones Criteria - Rheumatic Fever Criteria Mnemonic6:25 Rheumatic Fever Diagnosis7:15 Rheumatic Fever Treatment / Rheumatic Fever Prophylaxis LINK TO SOCIAL MEDIA: https://www.instagram.com/rhesusmedicine/ReferencesCenters for Disease Control and Prevention (CDC) (2025) Acute rheumatic fever: clinical guidance. Available at: https://www.cdc.gov/group-a-strep/hcp/clinical-guidance/acute-rheumatic-fever.htmlCarapetis, J.R., Beaton, A., Cunningham, M.W., Guilherme, L., Karthikeyan, G., Mayosi, B.M., Sable, C., Steer, A., Wilson, N. and Wyber, R. (2016) ‘Acute rheumatic fever and rheumatic heart disease', Nature Reviews Disease Primers, 2, 15084.MSD Manual Professional Editors (2024) Rheumatic fever. MSD Manual Professional Edition. Available at: https://www.msdmanuals.com/professional/pediatrics/miscellaneous-bacterial-infections-in-infants-and-children/rheumatic-feverNational Institute for Health and Care Excellence (NICE) (no date) Rheumatic fever. NICE Clinical Knowledge Summaries. Available at: https://cks.nice.org.ukStatPearls Authors (2025) Acute rheumatic fever. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing. Available at: https://www.ncbi.nlm.nih.gov/books/NBK594238/Therapeutic Guidelines Limited (2022) ‘Therapeutics for rheumatic fever and rheumatic heart disease', Australian Prescriber, 45(4), pp. 118–123. Available at: https://australianprescriber.tg.org.au/articles/therapeutics-for-rheumatic-fever-and-rheumatic-heart-disease.htmlDisclaimer: Please remember this video and all content from Rhesus Medicine is for educational and entertainment purposes only and is not a guide to diagnose or to treat any form of condition. The content is not to be used to guide clinical practice and is not medical advice. Please consult a healthcare professional for medical advice.

(00:00) The Golden Globe nominees for BEST PODCAST: Who's in? Who got snubbed?(17:39.04) TIM HEALEY from the Boston Globe joins Toucher & Hardy and share the latest from the Winter Meetings(32:18.78) Beaton had the sniffles and took a sick day. So Jorge is here and he chats it up with BLIND SCOTT.Please note: Timecodes may shift by a few minutes due to inserted ads. Because of copyright restrictions, portions—or entire segments—may not be included in the podcast.CONNECT WITH TOUCHER & HARDY: linktr.ee/ToucherandHardyFor the latest updates, visit the show page on 985thesportshub.com. Follow 98.5 The Sports Hub on Twitter, Facebook and Instagram. Watch the show every morning on YouTube, and subscribe to stay up-to-date with all the best moments from Boston's home for sports!See Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

Cecil Beaton fue mucho más que un fotógrafo: fue un arquitecto del glamour, un creador de mundos y un visionario que llevó la fotografía de moda a otro nivel. En este video exploramos su vida, sus influencias, los secretos detrás de sus retratos más icónicos y cómo su estilo sigue inspirando a fotógrafos, cineastas y artistas alrededor del mundo. Descubra cómo Beaton combinó teatralidad, elegancia y una estética única que marcó el rumbo del retrato moderno. Acompáñeme en este viaje visual por la obra del hombre que redefinió lo que es fotografiar belleza, sofisticación y carácter. Si le apasiona la historia de la fotografía, la moda o simplemente el arte de crear imágenes inolvidables, este video es para usted.#CecilBeaton #HistoriaDeLaFotografía #FotografíaDeModa #RetratoFotográfico #FotografíaClásica #FotógrafosLegendarios #ArteVisual #FotografíaVintage #IconosDeLaModa #MaestrosDeLaFotografía

In this episode of The Pet Food Science Podcast Show, Lindsay Beaton, editor of Petfood Industry magazine and host of Trending: Pet Food, unpacks how innovation, sustainability, functionality, and communication are shaping the modern pet food landscape. She explores evolving consumer expectations, the role of technology, and how industry leaders can maintain trust while advancing pet nutrition. Stay ahead of industry change, listen now on all major platforms!“Innovation in the pet food industry isn't just about invention. It's about creating value through new, meaningful ways that connect with modern consumers.”Meet the guest: Lindsay Beaton is the editor of Petfood Industry magazine and host of the Trending: Pet Food podcast, both published by WATT Global Media. With nearly two decades in business-to-business publishing, she brings deep expertise in industry communication and trends. Passionate about transparency and innovation, she connects science, market forces, and consumer behavior shaping global pet nutrition. Liked this one? Don't stop now — Here's what we think you'll love!Maïlys Le Thiec: Ingredient Quality & Palatability | Ep. 117Dr. Sara Martini: Microbiota & Nutrition | Ep. 115Dr. Sara Cutler: Shelf Life Science | Ep. 111Don't miss the chance to be part of the Pet Food Inner Circle!Join now and connect with leading experts in pet nutrition: https://petfoodinnercircle.com/What will you learn:(00:00) Highlight(00:43) Introduction(03:25) Defining innovation(09:58) Major industry trends(18:14) Communication challenges(27:53) Industry evolution(30:19) Longevity opportunities(38:14) Final QuestionsThe Pet Food Science Podcast Show is trusted and supported by innovative companies like:* Kemin* Trouw Nutrition- Biorigin

In this monthly conversation series Grant Scott speaks with art director, lecturer and creative director Fiona Hayes. In an informal conversation each month Grant and Fiona comment on the photographic environment as they see it through the exhibitions, magazines, talks and events that Fiona has seen over the previous weeks. Mentioned in this episode: https://thephotographersgallery.org.uk/whats-on/boris-mikhailov-ukrainian-diary www.npg.org.uk/whatson/exhibitions/2025/cecil-beaton/ https://www.youtube.com/watch?v=rLjkQyp2Bjk www.saatchigallery.com/exhibition/futurespective Fiona Hayes Fiona Hayes is an art director, designer, consultant and lecturer with over 30 years' experience in publishing, fashion and the art world. She has been a magazine art director ten times: on Punch, Company, Eve, the British and Russian editions of Cosmopolitan, House & Garden,GQ India (based in Mumbai), MyselfGermany (in Munich), and Russian Vogue (twice). Between 2013 and 2019, as Art Director of New Markets and Brand Development for Condé Nast International, based in London and Paris, she oversaw all the company's launches – 14 magazines, including seven editions of Vogue. She still consults as Design Director at Large for Vogue Hong Kong. In 2002 she founded independent photography magazine DayFour, publishing it continuously until 2012. She is Co-Author and Art Director of The Fashion Yearbook, and creative director of books for South African media consultancy Legacy Creates. Outside the publishing world, she has been Art Director of contemporary art auction house Phillips de Pury in London and New York, and Consultant Art Director of Russian luxury retail group Mercury/TSUM. (Fiona would like to point out she is not Russian: she is proudly Irish and studied Visual Communication and History of Art and Design at NCAD Dublin.) She currently divides her time between design consultancy for commercial clients, and lecturing at Oxford Brookes University, the Condé Nast College of Fashion and Design, London, Nottingham Trent University, Ravensbourne University, and Leeds University. She lives in West London. @theartdictator Dr.Grant Scott After fifteen years art directing photography books and magazines such as Elle and Tatler, Scott began to work as a photographer for a number of advertising and editorial clients in 2000. Alongside his photographic career Scott has art directed numerous advertising campaigns, worked as a creative director at Sotheby's, art directed foto8magazine, founded his own photographic gallery, edited Professional Photographer magazine and launched his own title for photographers and filmmakers Hungry Eye. He founded the United Nations of Photography in 2012, and is now a Senior Lecturer and Subject Co-ordinator: Photography at Oxford Brookes University, Oxford, and a BBC Radio contributor. Scott is the author of Professional Photography: The New Global Landscape Explained (Routledge 2014), The Essential Student Guide to Professional Photography (Routledge 2015), New Ways of Seeing: The Democratic Language of Photography (Routledge 2019), and What Does Photography Mean To You? (Bluecoat Press 2020). His photography has been published in At Home With The Makers of Style (Thames & Hudson 2006) and Crash Happy: A Night at The Bangers (Cafe Royal Books 2012). His film Do Not Bend: The Photographic Life of Bill Jay was premiered in 2018. Scott's next book is Inside Vogue House: One building, seven magazines, sixty years of stories, Orphans Publishing, is on sale now wherever you buy your books. ©Grant Scott 2025

o tym jak samowspółczucie pomaga mi w utrzymaniu równowagi psychicznej źródła i wykorzystane materiały: książka Kristin Neff: Neff, K., Germer, C. (2022). Samowspółczucie. Wykorzystaj techniki uważności, abyzaakceptować siebie i zbudować wewnętrzną siłę. Gdańskie Wydawnictwo Psychologiczne.książka Paula Gilberta: Gilbert, P., Choden. (2019). Uważne współczucie. Gdańskie Wydawnictwo Psychologiczne.strona Kristin Neff: https://self-compassion.org/ koło emocji: https://streskiler.pl/mapa-emocji-i-kolo-uczuc-powiedz-co-naprawde-czujesz/ badania: Beaton, D. M., Sirois, F., Milne, E. (2020). Self-compassion and perceived criticism in adults with attention deficit hyperactivity disorder (ADHD). Mindfulness, 11(11), 2506- 2518. https://doi.org/10.1007/s12671-020-01464-w Beaton, D. M., Sirois, F., Milne, E. (2021). The role of self-compassion in the mental health of adults with ADHD. Journal of Clinical Psychology, 78, 2497-2512. https://doi.org/10.1002/jclp.23354 Neff, K. D. (2023). Self-Compassion: Theory, Method, Research, and Intervention. Annual Review of Psychology, 74, 193-217.Dzwonkowska, I. (2013). Współczucie wobec samego siebie a inne wymiary osobowości oraz emocjonalne funkcjonowanie ludzi. Czasopismo Psychologiczne, 19(2), 303–312.Gilbert, P. (2014). The origins and nature of compassion focused therapy. The British journal of clinical psychology, 53(1), 6–41. https://doi.org/10.1111/bjc.12043Goetz, J. L., Keltner, D.,Simon-Thomas, E. (2010). Compassion: an evolutionary analysis and empirical review. Psychological bulletin, 136(3), 351–374. https://doi.org/10.1037/a0018807Kocur, D., Flakus, M., Fopka-Kowalczyk, M. (2022). Skala Współczucia dla Samego Siebie (SCS-PL). Przegląd Badań Edukacyjnych (Educational Studies Review), (37). https://doi.org/10.12775/PBE.2022.013Neff, K. D. (2003b). Self-compassion: An alternative conceptualization of a healthy attitude toward oneself. Self and Identity, 2, 85-102. zapraszam was na mojego: instagrama: ⁠⁠⁠⁠https://www.instagram.com/kasia_fatyga/⁠⁠⁠⁠tik toka: ⁠⁠⁠⁠https://www.tiktok.com/@kasiafatyga?lang=pl-PL⁠⁠⁠⁠maila: kasiafatyga.podcast@gmail.com oraz do obserwacji i oceny podcastu a jeśli uważacie moje treści za wartościowe (lub po prostu przydatne) i chcecie mnie w jakiś sposób wesprzeć możecie postawić mi wirtualną kawę na ⁠⁠⁠⁠⁠https://buycoffee.to/moje-adhd⁠ ⁠⁠⁠⁠z góry dziękuję za każdy rodzaj wsparcia ❤️

(00:00) Beaton's ear and Fred's algorithm are the topics during the show opening!(21:11) WHAT HAPPENED LAST NIGHT35:23(PLEASE be aware timecodes may shift up to a few minutes due to inserted ads)CONNECT WITH TOUCHER & HARDY: linktr.ee/ToucherandHardyFor the latest updates, visit the show page on 985thesportshub.com. Follow 98.5 The Sports Hub on Twitter, Facebook and Instagram. Watch the show every morning on YouTube, and subscribe to stay up-to-date with all the best moments from Boston's home for sports!See Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

In this episode of from the helm, Grady Wulff sits down with Cobram Estate Olives (ASX:CBO) Co-CEO, Sam Beaton, to explore the company's impressive FY25 performance, US expansion strategy, and premium olive oil brand growth.Sam shares insights into Cobram Estate's branded product sales, grove development plans, and investment priorities across Australia and California, while discussing how the company maintains its premium brand positioning in competitive markets.In this interview, Sam covers:• (0:41) an overview of Cobram and its core operations in olive farming and extra virgin olive oil production• (3:03) branded product sales growth in Australia and the US• (5:10) timeline and yield expectations for newly acquired California groves• (5:45) main operational risks including climate, water, and labour• (6:55) managing the 15% US price increase and consumer retention• (8:36) key investor news flow to watch over the next 12 monthsNote: This interview was filmed on 24 September 2025.

This is Amanda's experience of Turner SyndromeRelationship with Turner Syndrome[00:20] The Biggest Challenge of having Turner Syndrome[02:30]The Most Positive Experience of Having Turner Syndrome [07:05]How the Society has helped Amanda? [09:15]Whats Amanda's involvement in the society?[10:00]Most important message on Turner Syndrome[11:40]My instagram is https://instagram.com/turnersyndrometalkandtea?utm_medium=copy_linknMy facebook is https://www.facebook.com/EmilySeymour24aMy twitter is https://twitter.com/es_eymour?fbclid=IwAR2_PIoSVi47yeab3xnQFdPv0ae3NSEWwQahTHMIvloXbf_qetPOQPumQ1wIf you want to be a guest on my podcast then message me on any of my socials Want to know more about Turner Syndrome? Go to https://tss.org.uk/ and get more information.

Dr. Stephen Beaton is Co-founder and CEO of Circularity Fuels, which develops compact reactors that turn waste carbon streams into high-value fuels and chemicals. Rather than compete with fossil fuels from the start, Stephen identified high-purity methane for lab-grown diamonds as a beachhead market—where Circularity's product is 80–90% cheaper than incumbents while proving the core technology needed for clean liquid fuels.Stephen earned a chemistry PhD at Oxford and built deep expertise in synthetic fuels during his U.S. Air Force career, including overseeing jet fuel quality control in the Middle East and launching the Air Force's e-fuels program. His insight: build a fuels company that doesn't begin with fuel.Today, Circularity Fuels operates demonstration reactors in diamond facilities and is scaling toward biogas-to-SAF production using the same reactor platform. The company has raised $3M in venture funding, including from DCVC, plus $5M in grants from ARPA-E, NSF, and the California Energy Commission. MCJ is proud to be an investor.Episode recorded on Aug 12, 2025 (Published on Sept 16, 2025)In this episode, we cover: [03:09] Dr. Beaton's background in clean fuels[07:31] His work with Air Force petroleum in the Middle East[10:12] A brief overview of hydrocarbons[13:08] ESAF as resilience for Pacific operations[16:22] What e-SAF really means and why it matters[19:24] Circularity Fuels' origin story[21:20] The company's three principles[23:04] High-purity methane for diamonds as a beachhead[27:46] Recycling diamond exhaust with microwave-sized reactors[30:40] Building a fuel company without fuel as the initial product[34:35] Hardware sales vs metered methane service model[39:05] Biogas-to-SAF pathway via Fischer-Tropsch[42:38] Circularity's progress to date[44:01] Competing with fossil jet and carbon removals[48:41] How Circularity secured non-dilutive funding Enjoyed this episode? Please leave us a review! Share feedback or suggest future topics and guests at info@mcj.vc.Connect with MCJ:Cody Simms on LinkedInVisit mcj.vcSubscribe to the MCJ Newsletter*Editing and post-production work for this episode was provided by The Podcast Consultant

Stevie and Reidzo discuss; Kilmarnock 1-2 Celtic A drab first half A better second half A brave referee An excellent debut from Tounekti Improvement needed in the weeks ahead Music Credit - Instant Remedy Learn more about your ad choices. Visit podcastchoices.com/adchoices

Andrew Beaton joins JR to preview the upcoming NFL season.

With my special guest, Heather Beaton — Soul Psychology Coach, Executive Leadership Coach, and Founder of Illuminate: Unleash Your Inner Leadership Brilliance. ✨In this conversation, we explore two key intentions:That you walk away with a deeper awareness that everything you need to create a rich, thriving, and fulfilling life already lives within you — flowing from the inside out, rather than relying on the outside in.That you recognize self-worth and self-trust as the foundation upon which your Truth and Essence are built.Here's to your journey of self-worth and self-trust — anchored, grounded, and centered in your own inner wisdom, intuition, navigational system, and power. Meet Heather Beaton: Executive Leadership & Soul Care CoachHeather Beaton is an Executive Leadership & Soul Care Coach whose approach is grounded, direct, empathic, courageous, wise, and honest. She creates a sacred space where clients feel safe to gently lower their defenses, allowing their inner light to shine through. With Heather's guidance, individuals are continually invited to embrace the truth of who they are and lead from that place of authenticity.

Crimson Education head Jamie Beaton has set his sights on a new business venture. Concord Visa is an immigration consultancy project designed to streamline how startups and talent access new markets. Beaton explained how this venture would help people reach new oppurtunites. LISTEN ABOVESee omnystudio.com/listener for privacy information.

“Self-care is the beginning of a path to hope.” - Micky Beaton When life feels chaotic, self-care is usually the first thing to go (if it was even there in the first place). But for those of us living with fibromyalgia, that's when you need it the most. Deprioritizing the practices and tools that help you feel your best will lead to fibro flares, more pain, and less energy, making it even harder to keep up. Self-care doesn't have to be complicated, expensive, or time-consuming. It doesn't have to be treating yourself to something extravagant. At the core, self-care is about prioritizing your health and your body and treating yourself the way you'd treat someone you love. It means listening to your body, making small, deliberate choices that support your well-being, and letting go of the guilt that often comes with putting yourself first. When you make yourself one of your “favorite people,” you create the best chance for you to have a better quality of life. Today, Tami is joined by Certified Fibromyalgia Coach® Micky Beaton to talk about how you can create a reliable self-care routine that is sustainable and fits into your life. Micky was diagnosed with fibromyalgia over 20 years ago and spent many of the years since searching for answers. Recognizing that there were many other people out there with fibromyalgia who needed the right support, Micky joined the Certified Fibromyalgia Advisor® and then Certified Fibromyalgia Coach® training programs. In this conversation, Tami and Micky explore Micky's diagnosis experience and early struggles with fibromyalgia, the push-crash cycle she found herself stuck in for a long time, her path to life coaching, further education, and discovering fibromyalgia coaching, why what works for one person may not work for another, finding positives in chronic illness, Micky's ongoing learning and passion for coaching, her experience of mutual growth with clients since becoming a Certified Fibromyalgia Coach®, how coaching helps clients maintain self-care and accountability, creating flexible self-care plans, what self-care really means, myths about self-care, the connection between independence and community, practical tips for delegating and overcoming perfectionism, the importance of building a support team, the pillars of self-care, why you should be having conversations with yourself, how self-care became Micky's passion, how self-care supports medical treatments and calms the nervous system, where to start with self-care without feeling overwhelmed, how to fit self-care into already busy lives, why it's important to begin with easy actions and celebrate small wins, why you should trust in the process and stay hopeful, and more.       Note: This episode is not meant to be medical advice. Every person and every situation is unique. The information you learn in this episode should be shared and discussed with your own healthcare providers. To learn more about the resources mentioned in this episode, visit the show notes. For daily doses of hope, inspiration, and practical advice, join Tami on Facebook or Instagram. Need a good book to read? Download Tami's books for free. Ready to take back control of your life and health? Schedule a complimentary consultation with a Certified Fibromyalgia Coach®.  

Send us a textBack again for our weekly period drama and boy, did they not disappoint. From using children as collateral in card games to gruesome street accidents a la Meet Joe Black this episode had us locked in. So copper your shaft and look both ways because we only have two episodes left!Support the showVisit MummyDearestPodcast.com for merch and more!Follow the podcast on Instagram!Follow Sloane on Instagram!Follow Zach on Instagram!And most importantly, become a Patron and unlock hundreds of bonus episodes!

Saira Baker chats with senior curator of photographs at the Royal Collection Trust and curator of the exhibition, Alessandro Nasini, in The King's Gallery at the Palace of Holyroodhouse, Edinburgh.‘Royal Portraits: A Century of Photography' charts the evolution of royal portrait photography from the 1920s to the present day, revealing the stories behind the creation of some of the most iconic images of the British Monarchy.Bringing together more than 90 photographic prints, proofs and documents from the Royal Collection and the Royal Archives, the exhibition – which follows a successful run in London – will also consider the artistic and technological advances in photography as it evolved into a recognised art form.Visitors will see glamorous images from the first half of the 20th century, taken by some of the most respected photographers of the era. All of the photographs in the exhibition are vintage prints – the original works produced by the photographer – and the earliest works date from the 1920s and 30s, the golden age of the society photographer. In the mid-20th century, no royal photographer had a greater impact on shaping the monarchy's public image than Cecil Beaton. The exhibition will present some of Beaton's most memorable photographs, taken over six decades. These include Queen Elizabeth The Queen Mother's famed 1939 shoot in the Buckingham Palace Gardens, dressed in gowns designed by Norman Hartnell, and Beaton's original Coronation portraits of Queen Elizabeth II – arguably the most prestigious photography commission of the century.The bold and colourful later photographs in the exhibition will demonstrate the extraordinary variety, power, and at times playfulness of royal portrait photography over the past four decades. These works range from Andy Warhol's diamond-dust-sprinkled screen print of Queen Elizabeth II to well-known photographs by David Bailey, Nick Knight, Annie Leibovitz and more. The exhibition runs until 7 September 2025. For more information about the portraits discussed in this podcast, visit the Royal Collection Trust website and visit the exhibition in person. To book tickets and discover the events programme, see: https://www.rct.uk/collection/exhibitions/royal-portraits-a-century-of-photography/the-kings-gallery-palace-of-holyroodhouseTo find out more about visiting the other royal residences and exhibitions mentioned in the episode, see: https://www.rct.ukRoyal Collection Trust is a charity caring for the Royal Collection and welcoming visitors to the royal palaces. We bring our shared history to life through world-class experiences that involve and inspire people, wherever they are. Income from tickets and retail sales helps us to conserve the Collection so that it can be enjoyed by everyone for generations to come.

Today's Mystery: The lovely Ms. Beaton is caught in a lie, and then even more suspects emerge.Original Radio Broadcast Date: 1935 or 1936Originating in Los AngelesStarring: Walter Connolly as Inspector Charlie ChanSupport the show monthly at https://patreon.greatdetectives.netPatreon Supporter of the Day: James, Patreon supporter since October 2022.Support the show on a one-time basis at http://support.greatdetectives.net.Mail a donation to: Adam Graham, PO Box 15913, Boise, Idaho 83715Take the listener survey at http://survey.greatdetectives.netGive us a call at 208-991-4783Follow us on Instagram at http://instagram.com/greatdetectivesFollow us on Twitter @radiodetectivesJoin us again tomorrow for another detective drama from the Golden Age of Radio.

Guests include: Bryce Lance, NDSU senior wide receiver and; Mike Beaton, Fargo South Athletic Director

Heather Beaton: Tired of Being Nothing | The Hopeaholics PodcastIn this emotional episode of The Hopeaholics Podcast, Heather Beaton shares her powerful journey from homelessness and addiction to finding freedom through recovery. She opens up about the trauma that fueled her substance abuse, her struggles with violent relationships, and the repeated suicide attempts that marked her darkest moments. Heather discusses how resentment toward her family drove her addiction, the illusion of control she clung to, and the spiritual awakening that ultimately saved her life. Her story is a raw and inspiring testament to the power of recovery, faith, and the support of a compassionate community.#thehopeaholics    #redemption #recovery #AlcoholAddiction #AddictionRecovery #wedorecover  #SobrietyJourney #MyStory #RecoveryIsPossible #Hope #wedorecover Join our patreon to get access to an EXTRA EPISODE every week of ‘Off the Record', exclusive content, a thriving recovery community, and opportunities to be featured on the podcast. https://patreon.com/TheHopeaholics Follow the Hopeaholics on our Socials:https://www.instagram.com/thehopeaholics https://linktr.ee/thehopeaholicsBuy Merch: https://thehopeaholics.myshopify.comVisit our Treatment Centers: https://www.hopebythesea.comIf you or a loved one needs help, please call or text 949-615-8588. We have the resources to treat mental health and addiction. Sponsored by the Infiniti Group LLC:https://www.infinitigroupllc.com Timestamps:00:01:55 – Emotional Reflection on Her Transformation00:05:01 – Addiction in the Family00:10:12 – Surviving Domestic Violence00:12:15 – Resentment Driving Addiction00:17:29 – Suicide Attempt at 1800:21:52 – First Treatment Experience00:30:32 – Failed Sub-Maintenance Attempt00:33:14 – "God's Hole in the Wall" Metaphor00:35:14 – Accepting Powerlessness00:36:51 – Desperate Prayer in Detox00:43:12 – The Power of Meditation in Recovery00:46:18 – Letting Go of Control and Trusting God00:51:23 – The Turning Point That Led to Sobriety00:56:42 – Healing Through the Recovery Community01:08:25 – Staying Sober by Helping Others

Sarah Beaton is an intuitive coach and sound healer, and she is one of Kailea's most cherished mentors. In this episode Kailea and Sarah talk about: How Sarah helped Kailea through an incredibly difficult period of life Sarah's use of astrology as a coaching tool   What Kailea most needs to let go of The shadow side of coaching or of trying to ‘help' others Bridging the gap between millennials and baby boomers You can find Sarah's work on Instagram @sarahbeatoncoach or by visiting www.sarahssoundtuary.com    We are so grateful to our incredible sponsors. This episode is brought to you by:  Wild Kitchen: www.wildkitchen.ca Blossoming Heart Yoga: www.blossomingheartyoga.com Nature Space Resort:  www.naturespaceresort.com Infrared Fitness: www.infraredfit.ca   Join the conversation over on Instagram @inthisnewseason. To find out more about Kailea's practice visit www.kaileaswitzer.com. In This New Season is recorded and produced by Greg Alsop at Don't Wake Baby Studio: www.gregalsop.com  

The CFIB says Newfoundland and Labrador is one of the worst places in the country when it comes to red tape. Adrian Beaton is the owner of Jack Axes. He joined us with his thoughts on the report.

Brendan talks about the books he read in Quarter 3 of 2024. Join us, won't you?Heart-Shaped Box by Joe Hill (2007)Echopraxia (Firefall #2) by Peter Watts, Adam J. Rough (Narrator) (2014)Marple: Twelve New Mysteries by Naomi Alderman et al (2022)Seveneves by Neal Stephenson, Mary Robinette Kowal (Narrator), Will Damron (Narrator) (2015)Edge of the Wire by Scott Kenemore (2024)Dwellings (Dwellings #1-3) by Jay Stephens (2024)Death of a Maid (Hamish MacBeth #22) by M.C. Beaton (2007)This Is How You Lose the Time War by Amal El-Mohtar and Max Gladstone (2019)JAWS by Peter Benchley (1974)What did you read in Q3 of 2024? Share your reading over on Boardgamegeek in Guild #3269.

Brilliant Exiles, American Women in Paris, 1900 - 1939 At the Speed March 29 - June 22, 2025

In a Happier In Hollywood Bonus Book Club Episode, Liz and Sarah dive into their discussion of Richard Osman's new book, We Solve Murders. Does it qualify as a “cozy mystery?” Which character did HIH listeners like the most? And do most of us talk to loved ones who are no longer with us like one of the main characters, Steve, does? Plus so much more.  Get in touch on Instagram: @Sfain & @LizCraft Get in touch on Threads: @Sfain & @LizCraft Visit our website: https://happierinhollywood.com Join our Facebook group: https://www.facebook.com/HappierinHollywood/ Happier in Hollywood is part of ‘The Onward Project,' a family of podcasts brought together by Gretchen Rubin—all about how to make your life better. Check out the other Onward Project podcasts—Happier with Gretchen Rubin, and Side Hustle School . If you liked this episode, please subscribe, leave a review, and tell your friends! LINKS: We Solve Murders by Richard Osman: https://amzn.to/4gbQRzh The Marlow Murder Club: A Novel by Robert Thorogood: https://amzn.to/3ZOctfy The Quiche of Death: The 1st Agatha Raisin Mystery by M.C. Beaton:  https://amzn.to/3Bb44Jz The Charity Shop Detective Agency series by Peter Boland: https://amzn.to/3ZKQ4zw Vera Wong's Unsolicited Advice for Murderers (A Vera Wong Novel) by Jesse Q. Sutanto: https://amzn.to/3D9tgAM Photo by Jaredd Craig on Unsplash To learn more about listener data and our privacy practices visit: https://www.audacyinc.com/privacy-policy Learn more about your ad choices. Visit https://podcastchoices.com/adchoices

This episode is a conversation with Christine Leach of Balevulin, Tiroran. Originally from near Portsmouth, Christine has lived on Mull for many years. Christine runs Pennyghael in the Past Historical Archive. PPHA is a remarkable archive full of the most interesting materials that shines light onto the history of Brolas and its surrounds. I've always found Brolas here on Mull to be a very tricky area to define. There are Macleans of Duart, Lochbuie and Brolas, Duart and Lochbuie are easy enough to locate in your mind, but Brolas less so. It is for that reason and many more, that I wanted to talk with Christine. Christine's book Hebridean Healers, about the medieval Beaton family, who were located at Pennycross is out now and very much worth your while. It's a great resource to explore Mull's past. Christine was joined by Andrea Cameron, Elizabeth Carter and Miek Zwambourn in the writing of the book. We also talk about Christine's journey to coming to live on Mull, what brought her here and how it swiftly began to feel like home. There are many names mentioned from that past that I know many listeners will be delighted to hear again. Christine has given me loads of photos to help illustrate her story, so do have a look at whatwedointhewinter.com for episode links and more info. Thanks for listening!

I interviewed Nancy Beaton, Chief Revenue & Marketing Officer at Uphold, at the Ripple Swell conference.Topics: - Uphold is a RLUSD Exchange partner - USD Interest Accounts - Debit Card and Apple Pay - Upcoming new products - Wall Street's impact on Crypto Show Sponsor -

What’s Trending: Community members near a Tacoma park intended for kids are speaking up about the crime problems after a woman was found dead there. The striking Boeing machinists are slated to lose their healthcare on Tuesday. A mini mart in Shoreline has been robbed several times in just the last couple of months. The New York Times and Associated Press received blistering criticism after they tried to portray the former head of Hezbollah in a positive light. // LongForm: GUEST: Franklin County Auditor Matt Beaton explains why he’s suing the state over the new residency rule for voting. // The Quick Hit: Mitt Romney is under scrutiny for not endorsing Kamala Harris.  

Today Aimee sits down with Mere Beaton, founder of EcoEndurance. EcoEndurance creates meaningful movement experiences around the world that support local and Indigenous communities and highlight community-based conservation.  In 2025, The Running Kind will head to Ecuador with EcoEndurance for our own immersive running experience. The Running Kind group has two spots remaining for January 20-28. If you are interested, please contact Aimee at wearetherunningkind@gmail.com. In addition, Mere has a few spots remaining on her EcoEndurance trip January 6-14 of next year. You can apply to secure a spot for that trip here: https://www.ecoendurance.run/trips For more information on EcoEndurance or to connect with Mere… www.ecoendurance.run @EcoEndurance LinkedIn: EcoEndurance   You can find more information about The Running Kind here. https://therunningkind.net/ https://www.facebook.com/groups/therunningkind/ @therunningkind_ If you are looking for additional ways to support The Running Kind, check out our Patreon page! patreon.com/TheRunningKind Aimee Kohler  Founder of The Running Kind @aimskoh Produced by Aimee Kohler Music Dim Red Light by Don Dilego  

In our latest episode, our guests are The Workforce and Career Development Director Mac Beaton and three of his former electronics students, Andre Dabney, David Hall, and Jonathan Wright. They talk to us about how important career and technical education was for them in high school and what makes CTE even more important for students today.

This episode is replublished from earlier in the season.Jacob Beaton, an Indigenous farmer from British Columbia, shares his experiences and insights on various topics. He discusses his tribal name and the matrilineal society he belongs to. Jacob talks about living in a remote area and the challenges he faced while farming and homeschooling his children. He also shares his vision for an ideal educational system and the importance of problem-solving skills. Jacob highlights the agrarian roots of First Nations people and the impact of colonial policies on Indigenous food systems. Jacob Beaton shares his experience of running a training farm and the challenges faced by Indigenous Canadians. He discusses the stereotypes and misconceptions surrounding Indigenous people and the importance of revitalizing traditions. Jacob also highlights the need for local community resiliency and the impact of systemic racism on Indigenous communities. He shares the success and struggles of his training farm programs and the difficulties in securing funding. Jacob reflects on the benefits of raising children on the farm and the power and creativity of young people. He concludes by expressing his passion for Indigenous crops and his love for potatoes and squash. In this episode, the hosts discuss various topics in their 'Cussing and Discussing' segment. They talk about the annoyance of having boots everywhere during winter, the challenges of funding and business planning in farming, and the friction between white farmers and First Nations farmers.Key TakeawaysIndigenous nations were traditionally matrilineal societies, where names and property rights were passed through the mother's line.Living in remote areas can present unique challenges, but it also offers opportunities for self-sufficiency and a closer connection to nature.An ideal educational system should focus on building confidence, streaming individuals towards their interests, and developing problem-solving skills.First Nations people have a long history of agriculture and food production, which has often been overlooked or misrepresented.Colonial policies have had a lasting impact on Indigenous food systems, and there is a need for policy changes and greater recognition of Indigenous farming practices. Winter brings the challenge of having boots scattered everywhere in the house.Funding and business planning are difficult aspects of farming that require careful consideration.There is a need for better understanding and collaboration between white farmers and First Nations farmers to work towards common goals.Chapters00:00 Introduction and Tribal Name01:17 Matrilineal Society03:03 Location and Remote Living05:35 Growing People and Mixed Vegetable Farm07:01 Healthcare Experience in Mexico08:18 Homeschooling and Life Skills15:36 Ideal Educational System18:42 Background in Computer Science27:24 Transition to Farming35:44 Agrarian Roots of First Nations People46:36 Becoming a Lightning Rod47:17 Mystical Stereotypes48:16 Revitalizing Traditions49:32 Local Community Resiliency51:22 Roots of Racism53:13 Different Realities in the United States and Canada56:37 Challenges Faced by Indigenous Canadians59:10 Training Farm Programs01:05:21 Success and Struggles of the Training Farm01:11:29 Balancing Work and Family01:16:14 Barriers in Government Funding01:20:43 Raising Kids on the Farm01:27:20 Recognizing the Power of Children and Young Adults01:32:22 Dominating the County Fair01:33:17 Cussing and Discussing: Boots Everywhere01:35:16 Cussing and Discussing: Funding and Business Planning01:37:06 Cussing and Discussing: Friction Between White Farmers and First Nations FarmersThank you for...

This edition of Eponymous Foods features a beautiful dessert, some myth busting about a very common food's invention, and a very sweet finish with a much-loved candy.  Research: “160 Years of Neuhaus History.” Neuhaus Chocolates. https://www.neuhauschocolates.com/en_US/history/History.html Beaton, Paula. “The Origin of the Crepe is Shrouded in Mystery.” The Daily Meal. June 3, 2023. https://www.thedailymeal.com/1302745/origin-crepes/ “Belgian Pralines: A sweet but not so short history.” Discover Benelux. https://www.discoverbenelux.com/belgian-pralines-a-sweet-but-not-so-short-history/ Charpentier, Henri and Boyden Sparkes. “Life à la Henri: Being the Memories of Henri Charpentier.” Modern Library. 2001. Fertel, R. “praline.” In “The Oxford Companion to Sugar and Sweets.” Oxford University Press. 2015. https://www.oxfordreference.com/view/10 Grosley, Pierre Jean, and Thomas Nugent (tr). “A Tour to London, Volume I.” Lockyer Davis. 1772. Accessed online: https://archive.org/details/bim_eighteenth-century_a-tour-to-london-or-ne_grosley-pierre-jean_1772_1/mode/2up “John Montagu.” American Battlefield Trust. https://www.battlefields.org/learn/biographies/john-montagu “Maison de la Prasline Mazet.” France Today. June 14, 2012. https://francetoday.com/food-drink/maison_de_la_prasline_mazet/#fm-popup-modal-close “Making Crepes Suzette.” Auguste Escoffier School of Culinary Arts. July 31, 2014. https://www.escoffier.edu/blog/baking-pastry/making-crepes-suzette/ “The main ingredient of Crepe Suzette.” Le Parisien. March 20, 2016. https://www.leparisien.fr/archives/l-ingredient-principal-de-la-crepe-suzette-grand-marnier-mais-pourquoi-grand-20-03-2016-5642685.php “Sandwich celebrates 250th anniversary of the sandwich.” BBC. May 12, 2012. https://www.bbc.com/news/uk-england-kent-18010424 Stradley, Linda. “Sandwich History.” What's Cooking America. https://whatscookingamerica.net/history/sandwichhistory.htm Sybertz, Alyssa. “What are pralines, exactly?” Readers Digest. July 17, 2023. https://www.rd.com/article/what-are-pralines/ Toussaint-Samat, Maguelonne. “A History of Food.” Blackwell. 2008. See omnystudio.com/listener for privacy information.

JK Beaton, co-founder of China Product Pros, shares insights on product sourcing from China. He emphasizes the importance of working directly with factories rather than trade companies to ensure consistent quality and lower costs. JK also advises brands to negotiate with factories and ask questions to understand the challenges and find solutions. He highlights the risk of products being held ransom at port and recommends filing a trademark in China to prevent this. JK discusses the significance of on-site visits and inspections to maintain quality control. He also mentions emerging trends such as factories moving towards automation. Key Episode Takeaways: Work directly with factories to ensure consistent quality and lower costs Negotiate with factories and ask questions to understand challenges and find solutions File a trademark in China to prevent products from being held ransom at port Conduct on-site visits and inspections to maintain quality control Be aware of emerging trends, such as factories moving towards automation If you feel JK Beaton and his team at China Product Pros can help you, you may visit: https://www.chinaproductpros.com  For show transcript and past guests, please visit https://www.ecommercemarketingpodcast.com Or on YouTube at: https://www.youtube.com/channel/UC3PgT0NOGzpdPGQtBK0XLIQ  Follow Arlen: Twitter: https://twitter.com/askarlen   Facebook: https://www.facebook.com/arlen.robinson.7   Instagram: https://www.instagram.com/arlenyohance/   LinkedIn: https://www.linkedin.com/in/arlenrobinson/   Past guests on the ecommerce marketing podcast include Neil Patel, Nemo Chu, Luke Lintz, Luke Carthy, Amber Armstrong, Kris Ruby and many more. Thanks for listening. Be sure to subscribe and leave a review.

If you're a longtime listener, you know getting in front of borrowed traffic is our favorite audience growth strategy, and today's case study on hosting roundtables affirms why. Women's leadership expert and founder of Safi Media, Eleanor Beaton, has successfully hosted 14 roundtables since Q4 2021, inviting aligned speakers to join her for hot button conversations and growing her email list by 2655 highly vetted subscribers in the process.The roundtables may be free to attend, but they have collectively driven $884,000 in post-event sales from attendees.We ask Eleanor all the questions you want to know to replicate this strategy in your own business, from the logistics of promoting, inviting speakers, and facilitating roundtable conversations, to which roundtable topics drew the biggest crowds and how to best approach the post-event sales process without scaring your new leads away.View the transcript for this episode at: https://otter.ai/u/AUzgzZdRZJWN7Jrwsu956FWs-Bw?utm_source=copy_urlThank you to our sponsors!Learn how to sell (and scale!) your course or program on autopilot, every single day with Nicki's free video training: https://circuitsalessystem.com/ceoTransform your business and take your sales to the stratosphere with Coming Up Roses' course and marketing community, "Launch Your Own Way": https://cominguproses.co/lyowListen to Kelsey's case study: https://link.chtbl.com/NXHQOVSvTry the #1 all-in-one E-commerce platform: Shopify! Sign up for a one dollar per month trial period at https://shopify.com/ellenConnect with Eleanor:www.safimedia.co/roundtable Instagram: @eleanorbeatonIconic business leaders all have their own unique genius. Take this quick 10 question quiz to uncover your specific CEO style advantage: https://ellenyin.com/quizIf you enjoyed today's episode, please:Post a screenshot & key takeaway on your IG story and tag me @missellenyin & @cubicletoceo so we can repost you.Leave a positive review or rating at www.ratethispodcast.com/cubicletoceoSubscribe for new episodes every Monday.Join our C-Suite membership to get bonus episodes! Check out everything our members get at https://ellenyin.com/csuite

This week, I chat to Mike Beaton, a distinguished Royal Marine turned nutrition expert and endurance athlete. From the rigorous training grounds of the Royal Marines to challenging the limits in Ironman competitions, Mike has not only represented Great Britain seven times but has also been honoured with an MBE for his significant contributions to health and nutrition. In this episode, Mike shares his early childhood experiences, the pivotal moment he decided to join the Marines, and how these experiences shaped his unique "recipe for success." We'll explore his journey to receiving the prestigious MBE, his passion for educating the youth about diet and nutrition, and his rigorous training regimen that balances a demanding career with family life. Discover how Mike's military discipline transformed into his approach to endurance sports and nutrition, making him a revered figure in both fields. Whether you're a budding athlete, a nutritional enthusiast, or someone looking for inspiration to push your limits, Mike's insights offer invaluable lessons in resilience and dedication. This episode is a must-listen for anyone interested in the military world, sports endurance, and nutritional wisdom. --- Send in a voice message: https://podcasters.spotify.com/pod/show/alex-chisnall2/message

Narrators Natalie Beran and Jackson Bliss portray queer Russian-Maori siblings Greta and Valdin in this wise, hilarious novel about a loving and chaotic New Zealand family. Host Jo Reed and AudioFile's Emily Connelly discuss Rebecca K. Reilly's novel, now released in the U.S. Beran depicts Greta, a 20-something PhD student in a perky, wry tone that is dripping with millennial angst. Bliss narrates Valdin's sections with a mix of earnestness and detachment. A year after being dumped by his boyfriend, he's just (maybe) starting to get his life back on track. The narrators' varied New Zealand accents and ease with snappy dialogue make every moment of this joyful audiobook a pleasure. Read the full review of the audiobook on AudioFile's website. Published by Simon & Schuster. Discover thousands of audiobook reviews and more at AudioFile's website. This episode of Behind the Mic is brought to you by Brilliance Publishing. Revisit beloved characters and discover new original short stories. Visions of Flesh and Blood by Jennifer L. Armentrout with Rayvn Salvador is a must-add addition to the series that any fan will enjoy. Audible.com/VisionsofFleshandBlood This episode is brought to you by BetterHelp. Give online therapy a try at betterhelp.com/AUDIOFILE and get on your way to being your best self. Learn more about your ad choices. Visit megaphone.fm/adchoices

•Welcome to episode #383 of the 20MT Flagship podcast•More VAR nonsense at Livi•Reo Hatate returns for the Hoops•Who's starting in midfield?• Is this 'winner takes all'?•Is the Beaton appointment the SFA sticking two fingers up to Brendan Rodgers?and much moreWe're proud to support the Kano Foundation and are donating all of our YouTube revenue for the rest of the season. Check them out here - https://www.thekanofoundation.com/Treat yourself or the 20MT listener in your life, as well as supporting the podcast with some 20MT merch at 20mt.bigcartel.com/You can help support the production of these podcasts, as well as gaining access to over 920 extra episodes at patreon.com/20MinuteTimsSign up for Celtic's Youth Development Lottery The Celtic Pools and help shape Celtic's future here -https://celticpools.securecollections.net/index.aspx?Agent=3539Get 20% off and FREE shipping using the code TIMS at Manscaped.com20MT Hosted on Acast. See acast.com/privacy for more information.

Uncover the hidden talents of neurodiverse employees and learn how to support them in the workplace. In this episode of the HR Mixtape podcast, host Shari Simpson interviews Tara Beaton, an expert in disability management and accessibility. Tara shares her personal journey with ADHD and how it has changed her perspective on disability management. She emphasizes the importance of incorporating neurodiversity into the workplace and highlights the superpowers that individuals with ADHD can bring, such as creativity, pattern recognition, and hyperfocus. Tara also debunks common misconceptions about neurodiverse individuals and discusses the need for employers to create a culture of accommodation and inclusivity. Three key takeaways from this episode are: Disability management should include a focus on cognitive impairments and neurodiversity, just as it has addressed physical and sensory disabilities in the past. Neurodiverse individuals, such as those with ADHD, possess unique strengths and abilities that can benefit the workplace, including creativity, proactivity, and lateral thinking. Employers play a crucial role in fostering an environment where neurodiverse employees feel comfortable asking for accommodations. This requires creating a culture of inclusivity, questioning traditional norms, and being open to different ways of doing things. Guest(s): Tara Beaton, Owner, Tara Beaton

Josh Beaton of  www.joshbeaton.com and www.thetweenesteemproject.org creates and photographs luxury portraits with an edge. If you check out his clean but attention-grabbing website, you'll see he is one of Chicago's Premier Portrait Photographers. His portraiture has a distinctive, dark, romantic look, and it's easy to see why clients would be drawn [...] The post PBX551: Josh Beaton – How to use your photography to finance a passion project and get paid appeared first on Photography Business Xposed - Photography Podcast - how to build and market your portrait and wedding photography business.

Premium Members, click here to access this interview in the premium area Josh Beaton of  www.joshbeaton.com and www.thetweenesteemproject.org creates and photographs luxury portraits with an edge. If you check out his clean but attention-grabbing website, you'll see he is one of Chicago's Premier Portrait Photographers. His portraiture has a distinctive, dark, romantic look, [...] The post 551: Josh Beaton – How to use your photography to finance a passion project and get paid appeared first on Photography Business Xposed - Photography Podcast - how to build and market your portrait and wedding photography business.

House and Hubbard start the pod by going over Tom Kim's Shriners victory and Collin Morikawa's Zozo Championship victory (03:00). They also discuss Nathan's experience at Shriners and the energy around Lexi Thompson (13:50). Then, The Wall Street Journal's Andrew Beaton joins the show to discuss the ongoing Ryder Cup fallout (19:10), the current state of LIV Golf (28:07), and if the LIV-PGA deal will even happen (37:33). Hosts: Joe House and Nathan Hubbard Guest: Andrew Beaton Producer: Eduardo Ocampo Learn more about your ad choices. Visit podcastchoices.com/adchoices

Today I’m thrilled to have JK Beaton on the show. JK is a longtime student of my Create A Profitable Online Store Course and he runs a seven figure business selling home goods over at SaratogaHomeOnline.com. In this episode, you’ll learn how he got started and how he continues to scale his ecommerce business. Enjoy! What You’ll Learn How JK made his first organic sale A deep dive into JK’s home decor business How to create a successful kitchen storage business from scratch Other Resources And Books Saratoga Home Online Sponsors SellersSummit.com – The Sellers Summit is the ecommerce conference […] The post 501: Student Story – Making 7 Figures Selling Farmhouse Home Decor With JK Beaton appeared first on MyWifeQuitHerJob.com.

What's the most insufferably woke liberal city? Portland? San Francisco? Think again. Glenn Beaton became one of the most popular columnists in Aspen, Colorado, until he was abruptly fired on Christmas Eve for holding the wrong views. Now he has a new book, “High Attitude,” about how toxic wokeness wrecked one of America's nicest towns. Charlie talks to Glenn about that, then is joined by Ohio Senate candidate Bernie Moreno, who hopes to topple a vulnerable Democrat in 2024.Support the show: http://www.charliekirk.com/supportSee omnystudio.com/listener for privacy information.