Podcasts about rdr

Jose Youngs and Jed Meshew are here for another edition of SR LIVE! We cover it all form UFC 315, Alex Pereira HACKED, RDR vs. Whittaker NEXT?Bo Nickal's latest statement, Ian Garry for the belt, JDM or Belal and more!  Don't forget to use code "SUBMISSION" at https://Manscaped.com for 20% AND FREE SHIPPING (Plus you're helping the show) If you want to help the show please don't forget to SUBSCRIBE and give this video a like!

Teddy Atlas and co-host Teddy III cover all the fights from the past weekend. From Times Square, NYC card with Ryan Garcia and Rolly Romero as the main event to Riyadh Saudi Arabia for the Super Middleweight King Canelo's title defense vs William Skull and lastly, to Las Vegas, NV for Top 3 P4P Fighter Naoya Inoue's title defense vs Ramon Cardenas.Also, all undercard fight recaps in boxing as well as UFC Fight Night Coverage from Des Moines, IA.Thanks for being with us. The best way to support is to subscribe, share the episode and check out our sponsors:https://athleticgreens.com/atlas Timestamps:00:00 - Intro06:05 - Lopez vs Barboza11:20 - Haney vs Ramirez21:27 - Garcia vs Romero40:15 - Haney vs Garcia 243:45 - Bakole vs Ajagba51:55 - Surace vs Munguia 01:01:41 - Canelo vs Scull01:21:30 - Espinoza vs Vasquez01:34:25 - Inoue vs Cardenas1:48:55 - RDR vs Nickal02:00:20 - Sandhagen vs Figueiredo TEDDY'S AUDIOBOOKAmazon/Audible: https://amzn.to/32104DRiTunes/Apple: https://apple.co/32y813rTHE FIGHT T-SHIRTShttps://teddyatlas.comTEDDY'S SOCIAL MEDIATwitter - http://twitter.com/teddyatlasrealInstagram - http://instagram.com/teddy_atlasTikTok - https://twitter.com/Teddy_Atlas_RealTHE FIGHT WITH TEDDY ATLAS SOCIAL MEDIAInstagram - http://instagram.com/thefightWTATwitter - http://twitter.com/thefightwtaFacebook - https://www.facebook.com/TheFightwithTeddyAtlasThanks for tuning in. Please be sure to subscribe! Hosted on Acast. See acast.com/privacy for more information.

Fraudology is presented by Sardine. Get your tickets to Sardine[Con] and end the scamedmicIn this episode of Fraudology Karisse Hendrick provides important updates on Visa's Acquirer Monitoring Program (VAMP) and explores how recent tariffs are impacting e-commerce fraud. Hendrick explains that VAMP implementation has been delayed until October 1st, with fines not taking effect until January 2024. She clarifies that acquirers will likely pass VAMP fees onto merchants exceeding certain fraud ratios. Notably, Visa is expected to announce that alerts from Ethoca, CDRN, and RDR will now count towards reducing merchants' fraud ratios - a significant change from previous announcements. Hendrick also discusses how post-authorization systems may be negatively impacted by VAMP and Visa's new enumeration program.The episode then delves into the fascinating ripple effects of recent tariffs on e-commerce fraud patterns. Karisse shares insights from conversations with retail executives, revealing how tariffs are leading to customs delays, increased chargebacks, electronic stockpiling that triggers fraud systems, and the creation of "straw merchants" to avoid fees. She explains how fraudsters are exploiting Canadian accounts for cross-border schemes and how freight forwarding services are surging. Throughout, Hendrick emphasizes how these trends are straining fraud departments and forcing them to re-evaluate what constitutes suspicious behavior.Don't miss the eye-opening insights - tune in now to stay ahead of the latest fraud trends and regulatory changes!Fraudology is hosted by Karisse Hendrick, a fraud fighter with decades of experience advising hundreds of the biggest ecommerce companies in the world on fraud, chargebacks, and other forms of abuse impacting a company's bottom line. Connect with her on LinkedIn She brings her experience, expertise, and extensive network of experts to this podcast semi weekly, on Tuesdays and Thursdays.

The gang comes together to discuss the Bo Nickal hype train coming to a screeching halt. They talk about what wrong for Bo and what went right for RDR. They also discuss all the terrible boxing last weekend and sing Inoue's praises for doing his best to save the weekend. The gang also talks about their impressions of The Smashing Machine trailer and their expectations for the film. They then make their picks for the very solid UFC 315 main card including the two title fights. The gang then pays tribute to Mexico with their top 5 list. All that and another edition of "Stuff We Like."

On this episode of Good Guy / Bad Guy…is Bo Nickal overrated? Well, some are calling Reinier de Ridder the Conductor this morning after he put a stop to the Bo Nickal hype train in Des Moines, Iowa. Find out whether DC & Chael agree on Bo being overrated or RDR being underestimated. Plus, will Cory Sandhagen become the Bantamweight Champ in 2025? It's a question deserving of a hot take after Sandhagen called for the next title shot after beating former Flyweight Champ Deiveson Figueiredo.  Then, UFC 315 is on deck and we're breaking down why Belal Muhammad and Jack Della Maddalena are both looking past each other ahead of their Welterweight title bout. And we're celebrating Cinco de Mayo with the list of the greatest Mexican UFC fighters of all time. Find out who cracked the Top 3! Learn more about your ad choices. Visit podcastchoices.com/adchoices

Wat een nacht voor ons Nederlandse MMA liefhebbers! Reinier de Ridder sloopt Bo Nickal met zijn knieën tijdens UFC Des Moines. Kansloos was Bo Nickal tegen RDR. De volgende tegenstander van Renier? Als het aan hem ligt is het Reinier de Ridder vs Sean Strickland, wie weet in Nederland?! Ook kijken we vooruit op UFC 315, Belal Muhammed vs Jack Della Madalena. Blijft Belal champ? Of heeft de WW divisie weer in nieuwe champ in de vorm van JDM?Like, subscribe en gooi die 5 sterren op Spotify!Follow the socials:YT: ⁠⁠https://www.youtube.com/@buitendekooi ⁠⁠IG: www.instagram.com/buitendekooi TikTok: ⁠⁠https://www.tiktok.com/@UCTLy5wrugZswxF0_AU0o6sQ

On today's episode, I tell you why I have a problem with Islam Makhachev basing his future on the outcome of Belal Muhammad vs. Jack Della Maddalena. And for everyone doubting Kamaru Usman ... have you forgotten who Kamaru Usman is?Then,  I look ahead to Bo Nickal vs. Reinier de Ridder this weekend at UFC Des Moines, but apparently, Nickal weighed needs to cut a considerable amount of weight this week. I'll also tell you whether I agree with Vegas, who has Nickal as the heavy favorite. Next, UFC analyst Din Thomas thinks Jon Jones may never take the fight with Tom Aspinall, and I can tell you this matchup is definitely losing steam. Also, Eddie Hearn told Ariel Helwani that MMA is struggling, and I disagree. And finally, I have some PR advice for Francis Ngannou after hearing his name floated as a potential opponent for Eddie Hall.To support this program, please leave me a review on Apple Podcasts or submit a rating on my Spotify page.CHAPTERS:Makhachev's future (00:00)Doubting Kamaru Usman (12:11)Nickal weighs in at 222 pounds (22:29)Nickal vs. RDR (30:59)de Ridder respects du Plessis (39:48)Din Thomas: Jones may never fight Aspinall (47:37)Eddie Hearn: MMA in a recession (57:13)PR advice for Ngannou (01:04:56)

Le prime pagine dei principali quotidiani nazionali commentate in rassegna stampa da Davide Giacalone. Trump e i super dazi alla Cina, la sentenza su Turetta, i biglietti del Colosseo. #Ilpostinazienda. RDR è un'azienda del settore idraulico, specializzata nella progettazione, costruzione, gestione e manutenzione di acquedotti e impianti di trattamento acque in tutto il territorio italiano. Ha sedi operative in Lombardia, Sardegna, Puglia, Toscana e Lazio. Ha 450 dipendenti e ne cerca più di 20 con urgenza. Con noi Alessandro Di Ruocco, amministratore delegato di RDR. Don Antonio Mazzi, fondatore della comunità Exodus, regala ogni giorno un pensiero, un suggerimento, una frase agli ascoltatori di RTL 102.5. Ieri sera in campo la Uefa Champions League. All'Allianz Arena di Monaco di Baviera, l'andata dei quarti di finale tra Inter e Bayern Monaco. Il commento del nostro inviato Paolo Pacchioni.

La Perrada | ¡Se viene la revolución! Rubén Rdríguez toma el set de La Perrada y se sienta POR PRIMERA VEZ en la silla presidencial... con una sorpresa tras su entrevista con André Pierre Gignac y lo que dejó su visita a Tigres. Argentina APLASTÓ a Brasil (y con boleto previo en mano para el Mundial), se convirtió en la primer selección de Sudamérica en calificarse a la Copa del Mundo de 2026. Moraleja: NO hay que hablar antes de un partido. Los jugadores de la albiceleste hicieron muchas referencias a las palabras de Raphinha previas al encuentro. ¿Están listos para la era post Messi?Russel Wilson nuevo QB de los Giants, y puede haber un efecto dominó en la NFL, además, nuestro invitado Joshúa Maya nos trae un Stake House cargado de NBA para cobrar las tres posturas. Estamos disponibles en todas las plataformas digitales como @somoslaperrada , síguenos y forma parte de la manada más grande... exclusivas, información y los mejores picks ¿Dónde más?

In today's episode, Fares and Josh kick things off by discussing the recent TikTok drama and its near-deletion (2:25), plus the viral footage of Conor McGregor rubbing shoulders with Jake and Logan Paul on a bus (4:36). Then, they dive into the latest UFC 313 announcements, including Alex Pereira vs. Magomed Ankalaev (7:25) and Justin Gaethje's return against Dan Hooker (11:56).Next, they break down last weekend's UFC 311 card, starting with overall impressions (13:21). Payton Talbot's tough loss (17:25), RDR's dominant performance over Kevin Holland (20:20), and the instant classic Jiří Procházka vs. Jamahal Hill (27:48). In the co-main event, Merab Dvalishvili shocked everyone (33:38), and Islam Makhachev cemented his place as the top pound-for-pound fighter by defeating Money Moicano (44:20).To wrap things up, the boys give a quick preview of this Friday's boxing showdown: Naoya Inoue vs. Ye Joon Kim (53:40)Follow the podcast on IG:  https://www.instagram.com/thehbpod_/

Well hardy har, Mary, it's another episode of RDR. On the plus side, we get the recognition that cigarette moms deserve (and a future episode dedicated to the topic), RuPaul gives it some of her all as the musical guest and Paul W Downs is more than just a pretty face. We have tangents on lesbian voice, another important Rue and this season's parallels to Season 5, we're concerned for a certain roller skating grandma auntie who does financial training, and our tinfoil hats are firmly pinned on for this Badunka Dunk sponsored by Las Vegas situation.Become a Matreon at the Sister Mary level to get full access to Canada's Drag Race this season, plus movie reviews and past seasons of US Drag Race, UK, Canada, Down Under, Espana, Global All Stars, Philippines and more.Join us at our OnlyMary's level for EVEN MORE movie reviews, brackets, and deep dives into our personal lives!Patreon: www.patreon.com/alrightmaryEmail: alrightmarypodcast@gmail.comInstagram: @alrightmarypodJohnny: @johnnyalso (Instagram)Colin: @colindrucker_ (Instagram)Web: www.alrightmary.com  

Brendan Schaub recaps UFC 311 and talks Arman Tsarukyan pulling out due to a "back injury", why Islam Makhachev needs to go up a division next, why Jiri Prochazka needs to fight Robert Whittaker next, why Payton Talbott needs more time, why Islam Makhachev is the best pound for pound fighter at the moment, RDR finally showing his true talent, Merab's Dvalishvili cardio being the best in the world and much more. DraftKings - Download the DraftKings Sportsbook app NOW and use code SCHAUBSHOW Prolon - https://prolonlife.com/schaub for 15% OFF Progressive - https://www.progressive.com/ Sure Shot - https://sureshot.com/ Use code Brendan for 10% OFF Transcendcompany.com/BrendanSchaub - new customers get up to 15% off

NOTE: This podcast is not streamed in 4K. 0:00 - 4K gaming isn't as easy as getting a PS5. You need a 4K TV. And if you want to stream them you need a 4K capture card. And a 4K switcher. And 4K HDMI cables. 9:13 - Ghost of Tsushima is Horizon: Zero Dawn with different packaging. Which is fine because I like that game! 36:05 - I just can't force myself to enjoy Frieren: Beyond Journey's End so I've been trying some other new anime If you missed Saturday's live broadcast of Molehill Mountain, you can watch the video replay on YouTube.  Alternatively, you can catch audio versions of the show on iTunes. Molehill Mountain streams live at 7p PST every Saturday night! Credits: Molehill Mountain is hosted by Andrew Eisen.  Music in the show includes "To the Top" by Silent Partner.  It is in the public domain and free to use.  Molehill Mountain logo by Scott Hepting. Chat Transcript: 7:16 PMaddictedtochaos​​That is something I hope Nintendo gets away from with the next Zelda game. 7:18 PMaddictedtochaos​​It is absolutely possible to do a linear story in a non-linear world, look at GTA V and RDR. 7:22 PMLynndy Lee​​hello 7:37 PMSheekago​​Hey all 7:54 PMLynndy Lee​​gone were the days you almost get run over by a truck and transported into another fantasy world 7:54 PMWarren Lewis​​Hi! I forgot that today was Saturday. Hope things are well. 8:02 PMaddictedtochaos​​Will and Elizabeth

In the first episode of the new year, Fares and Josh kick things off by sharing their thoughts on the year so far (0:32), before diving into the bombshell that shook the MMA world: Arman Tsarukyan is out of the main event, courtesy of a last-minute shakeup from Dana White (7:11).P4P king Islam Makhachev now faces the charismatic "Money" Renato Moicano in a must-see main (13:43). In the co-main event, reigning champ Merab Dvalishvili defends his title against the undefeated phenom Umar Nurmagomedov in a fight that could define a division (20:33).The excitement continues with a heated battle between Jiri Prochazka and Jamahal Hill (29:29), a clash of grappling titans as Jailton Almeida takes on Serghei Spivac (35:21), a fan-favorite bout featuring Kevin Holland and RDR (37:08), and rising star Payton Talbott's next big moment (40:38).it's going to be a wild start to the year!https://www.instagram.com/thehbpod_/

In this episode, we explore the importance of patient involvement in shaping rare condition research initiatives. Our guests discuss why it's crucial to involve individuals with lived experiences, including patients and caregivers, in setting research agendas. In doing so, this approach ensures research can be more inclusive, efficient, and impactful, addressing the issues that matter most to those affected. Mel Dixon, Founder Cure DHDDS and member of Genomics England Participant Panel is joined by Jo Balfour, Founder of CamRARE and Dr Rona Smith, Senior Research Associate at the University of Cambridge and Honorary Consultant in Nephrology and Vasculitis. Find out more about the Cambridge Rare Disease Research Network, discussed in the episode, which aims to support the rare condition community in building an online network of partnerships and resources to facilitate new patient-centred research opportunities. "We're really turning research on its head, moving away from it being a researcher-led activity where they decide on the idea and the research concept and bring patients in at different points along that research journey and instead starting with the patient's idea in the first place.  It can only be a better system for all because it improves efficiency, it improves potentially the long term outputs and, most importantly, outcomes for patients." You can download the transcript or read it below. Mel: Welcome to Behind the Genes. Rona: I think it really means that we measure what matters to patients and individuals that are affected.  Often, it's really difficult to capture kind of the real impact of disease and there's a tendency for researchers to measure things that are easy to measure and are reproducible, which of course is important but what's most important is actually being able to truly capture the impact of an intervention on an individual's condition.  So, I think that's another key aspect of having people with lived experience involved right from the start. Mel: My name is Mel Dixon and I'm a member of the Participant Panel at Genomics England and founder of Cure DHDDS, a charity set up to raise awareness, support families and help drive research into the ultra-rare DHDDS gene variant.  On today's episode I'm joined by Jo Balfour, Managing Director of CamRARE, which is the Cambridge Rare Disease Network.  This network unites patients, advocates, experts and leaders to address the challenges faced by people affected by rare conditions.  I'm also joined by Rona Smith, Associate Professor at the University of Cambridge and honorary consultant in nephrology and vasculitis.  Today we'll be discussing the role of patients in setting research agendas and how their involvement can lead to more impactful and patient-centred research.  If you enjoy today's episode we'd love your support.  Please like, share and rate us on wherever you listen to your podcasts. Before we begin the interview I'd like to share a little bit of my story.  In November 2022, following whole genome sequencing, we received the news that two of our three children carried a neurodevelopmental and neurodegenerative DHDDS genetic variant.  At the time of our children's diagnosis there was very little information on our gene, minimal research happening into it and no treatment pathway.  Through our charity, Cure DHDDS, we have worked tirelessly to instigate research and create a collaborative scientific research community.  I am a huge advocate for patient-led research and have witnessed first-hand the positive impact it can have on patient lives.  Thanks to the work of the many scientists that we have had the honour of collaborating with, within two years of our children's diagnosis we have a disease-modifying therapy in our sight and an ASO (Antisense oligonucleotides) therapy in development.  We are incredibly grateful for the opportunities genetic testing has given us but I also appreciate how overwhelming a genetic diagnosis can be and how challenging it can be for families to initiate research projects with little to no resources, and that's why initiatives such as CamRARE that we'll be discussing today are so important.   On that note, let's get back to our podcast guests.  I wonder before we dive into today's topic if you could both give a brief introduction, and, Rona, if you could also give the less scientifically-minded of us an explanation about what nephrology is. Rona: Thank you for inviting me today.  So I'm Rona Smith, I work in Cambridge and I'm a nephrologist and that means somebody that looks after individuals who have diseases that affect their kidneys.  My specialist interest is in something called vasculitis which is a rare autoimmune disease that affects all organs in the body but kidneys as well.  Mel: Thank you.  And Jo?  Jo: Hi Mel.  I'm Jo Balfour, the Managing Director and one of the founding members of Cambridge Rare Disease Network, or CamRARE for short.  I think we're often described as the ‘Chief Everything Officers'.  I manage the charity and all of our operations and our wonderful team.    Mel: Lovely.  Thank you very much.  Rona, I wonder also if you could explain to our listeners what is a research agenda?  Rona: So in brief a research agenda is really a strategy that outlines key questions or topics that a research community, and that might be investigators, clinicians, scientists, patients, industry,  and they are the priorities that they want to explore and address over a period of time.  So it's really a direction of travel and identification of areas of importance and where there are gaps in knowledge so that it then leads to the opportunity to form specific research questions that you can then go on and address.  Mel: Why do you both think it's important to involve patients in setting these research agendas?  Jo: Well I think critically one of the things that I've learnt over my time working, not just in the rare disease sector but also earlier in social care and education, is that we should as professionals never assume anything; you know, we have not lived in their shoes and we don't know what the daily life of people living with rare conditions is like.  So gathering that day to day lived experience is really crucial.  And I have a unique opportunity to see into that daily life with our local community of rare disease families who have a range of different rare conditions.  I'm party to their conversations, to their daily trials and tribulations, the things that are difficult, the things that they find joy in but I still will always go back to them and ask their opinion.  I see myself as a spokesperson for them as we're an umbrella organisation but I certainly never really know what it's like to live with their conditions.  I think they bring with them diverse experiences which we really need and value in setting research priorities, they have unique knowledge of their own conditions.  They ethically have a right to be involved from the start and to set that priority and agenda but, equally, it's valuable for us as researchers because if we can involve people early we have definitely more chance of good engagement and later success, better outcomes for everyone.  Mel: Couldn't agree more.  And, Rona, is there anything you'd like to add to that? Rona: I think it really means that we measure what matters to patients and individuals that are affected.  Often it's really difficult to capture kind of the real impact of disease and there's a tendency for researchers to measure things that are easy to measure and are reproducible, which of course is important but what's most important is actually being able to truly capture the impact of an intervention on an individual's condition.  So I think that's another key aspect of having people with lived experience involved right from the start.  Jo: Another thing that's actually quite interesting that I'm going to mention here is that I think when you live day in, day out with a condition your perception of things like pain is different from your average person's so you become almost accepting of your daily norm, and I think that's really critical to understand as well.  And it's only by getting to really know patients and understand. When we say, “What's your pain like on a scale of 1 to 10?” you know, something that I feel as pain because I get it rarely I probably am going to put it at a higher score than somebody who has that every day.  So I think there's subtleties and nuances like that as well which are really critical to get across by conversation with patients.  Mel: That makes absolute sense.  And I see that from the patient perspective myself.  I was out with my friends the other day and they said, “Oh my goodness, you're constantly taking your children to sports activities.”  Because of their physical needs we're constantly,  they go to Pilates, they go to swimming, they go to gym class – we try to keep them fit and healthy – and we, even though they're older, have to take them there and back and that's become our norm but when you're speaking to families whose children don't have those difficulties they have no idea how much time that actually takes up.  And I had no idea how much like time it takes up compared to what other people are doing because that is our norm, that's what we've accepted as the norm.  Patients and patient groups are incredibly driven and invested in their rare disease as well so they make really good rare disease research partners.     And, moving on, what do you see as the challenges and barriers to patient involvement and how do we overcome these? Rona: I think probably the biggest barrier is time.  So, the most important thing is investing time to build relationships, to really understand in-depth perspectives both from the patient's side but also the researcher's side. And, inevitably, we always want to do things faster and actually this is one really, really critical aspect is investing time.  Funding is also a challenge.  Often you have to do a lot of upstream work before you have got funding for a project and that takes time from individuals and that's another challenge.  And I think the third thing for me is individuals that are patient partners in research, they're not just patients, they're people - they have lives, they have work, they have families, they have everything else that goes on in life - and so actually fitting this all in is really challenging.  Mel: Jo, is there anything you'd like to add there?  Jo: Yeah, I think just a word about diversity really and, you know, how do we uncover those hidden families and patients who currently don't really have a voice.  I think we'd all acknowledge that there are key voices within the rare disease community who will share the views of their community and they've become well-oiled machines almost at being great advocates but, as I mentioned earlier, even though I'm perhaps one of those people, you know, I speak for a community, I would never assume anything.  So, I still need to uncover the thoughts and the feelings and the emotions and the needs and the what matters from those people, and, as Rona mentioned, that takes time and it takes building relationships and trust with people.  So, we have a wonderful community in the Eastern region of England which is made up of families affected by all different rare diseases, and undiagnosed.  And some are babies and have been lucky enough to get a very early diagnosis and others are young adults but what we're finding through that is that experience is diverse and experience changes over time as families go through transition periods or they meet a roadblock and they're having to navigate things differently.  So, it's about building those relationships.  That takes times, it takes resources, it takes sometimes a reset in the way that we think things need to be done.  So instead of asking questions all the time and putting surveys out and trying to get response that way it takes a bit of thinking about how do we listen better and how do we give those people who don't have a voice, who are non-verbal or perhaps have a learning disability, how do we ensure that we're capturing their views as well.    And we did a really lovely project actually last year, it was something funded by the NHS called My Story, My Way, where we actually spent three months with our young adults working out what it was they wanted from our community next, how did they want us to follow them into adulthood.  And we knew that there were a number of young people in that group who were non-verbal and had some learning differences and we knew that we couldn't just do it in the normal format, we couldn't just do a focus group and ask their opinion, so we actually did it through photography.  So each of the familiess well, the young person themself was given a simple camera.  They basically had thirty-six shots.  You got thirty-six clicks to capture the things, the people, the places that you love and then to share them with us as a community.  And then we all discuss, you know, how these things might be something we can build into our future plans for them.  And it was such a wonderful activity.  We gave them plenty of time, plenty of opportunities to ask questions.  If the young person themself couldn't physically click the camera their sibling got to help them.  And their sibling or their parent was given another camera in black and white so we had distinctive pictures, pictures that the kid themself had taken, pictures that the family had taken, but all together, you know, it gave this lovely kind of medley, this beautiful visual representations of what mattered to them.  And I think it's about taking the time to be creative with people like that and really get to the bottom of “How do we find out what matters to you?” Mel: Although it takes time to think about those ideas.  That could be translatable across the board really, couldn't it, throughout various conditions.  I think that's fantastic.  Rona, I wonder if you can tell us how has the work that's already been done through the patient-led research hub facilitated addressing research priorities.  Rona: So just a tiny bit about the patient-led research hub.  So, this has been now running for nearly ten years through Cambridge.  It's a partnership between the Cambridge Biomedical Research Campus and we're based within the university and the Trust.  And in essence it kind of was set up because of really a mismatch between what many patients wanted from research and what investigators' views were.  And so really the premise is that we welcome patients to come to us with an idea, a problem, an unmet need in their disease area – and we do focus on rare disease – and we work with them to see “Well actually what do we already know about that?” and then if there is a gap in knowledge we then move to kind of trying to work and develop a question that we can then address.  And that might be a question that's addressed through generating more information through surveys or it may actually be a question of an intervention that we can test.  So, we've had lots of projects come through and we, just an example of a project was from a group of patients with a rare kidney condition called autosomal dominant polycystic kidney disease, and that is a condition where over time you accumulate cysts in your kidneys and the kidneys become large, they become very painful and eventually they can fail.  And a question that the patient group had was about whether drinking more water could impact the rate of growth of these cysts, and there's a strong hypothesis behind that that drinking lots of water reduces down the level of a particular hormone.  And we actually worked with the charity behind this group, the Polycystic Kidney Disease Charity, and designed a study to test a very high water intake to a normal water intake to see whether it was possible over a period of eight weeks for patients to actually stick to this.  It's quite difficult to do.  And they recorded how much water they'd drunk, they tested their own urine and actually it showed that this was feasible to do this kind of work.  So, I think the patient-led research hub is kind of taking the research priorities that are important to patients but working in a patient-led way to come right through to a project.  Mel: That sounds great.  And if the patients are engaged from the start of the project and it's led by them they're obviously going to be much more driven to take part in the actual research and see the research through themselves.    So, Jo, I'm very excited to hear about the launch of the Rare Disease Research Network.  Can you please tell me what the research network is and what you hope to achieve with it?  Jo: So the Rare Disease Research Network is first of all a bit of a mouthful so we're going to try and encourage people to call it the RDRN.  It's a co-created project which really the patient-led research hub in Cambridge approached us about in 2022, I think, we started talking about this, approached CamRARE as a partner to apply for an NIHR partnership grant, and we were successful with that to really take the model that the patient-led research hub had already developed and found was successful, and perhaps too successful for its own good – they were receiving more applications and more ideas than they could manage – and to develop that into an online platform.  So taking the same model, making it more accessible to a wider group of people, potentially worldwide, and providing the hand-holding that the patient-led research hub has always done, helping patients really consider their question, formulate that into a research idea, then do the literature search to find out “Is this question already answered, and if it is, great, can we provide that information to our community?  If it's not, how do we then build a team?  Who needs to be in my research team?  How do we then get funding together to take this idea forward?”  So, it's really taking the model, taking the good practice that already existed and creating an online platform to really attempt to replicate that as best we can. So the platform will launch on 23rd November (2024) at CamRARE's Rarefest which is a lovely in-person activity that's going on in Cambridge, and that platform will be open to anyone who has an interest in rare disease research.  But I think, critically, what's different about this is that, you know, we've talked about setting research agendas and we've talked about patients contributing to that, contributing to setting the priorities, what's different here is that the patients decide on the questions; it's what matters to the patients coming from them and their community.  And it's an opportunity for them to showcase those questions and those idea on a platform and almost to have a call to action, “Is there anyone else on this platform who has similar research interests to me?”  The platform will matchmake them together through a series of choosing tags, choosing tags about particular disease areas -  It's linked to the Orphanet database - choosing tags about the type of research that you're interested in.  That matchmaking process will happen, which at the moment is a very serendipitous process but we hope to take it a little bit further on from that.  It's still going to be a little bit of potluck who's on the platform at the time who's got similar interests as you but hopefully it will improve that serendipitous system.  And it will allow them to access resources on the platform, which is the kind of hand-holding bit, and also, critically, some mentoring.  So, there's a real sort of opportunity here for professionals – researchers, industry partners, healthcare professionals – who have particular skills in research to be able to say, “Well I can help.  I might not be able to be part of your team at this point but if you need half an hour on a Zoom call with me to think about your research question I can offer to mentor you on that.”  But, likewise, I think there's going to be lovely opportunities here for patient groups to support each other too because what we've always realised is that patient groups are at different points of their research journey.  You know, we see some organisations that are really well-funded now who are in partnership with industry, you know, they have a group of pharma companies that are supporting the development of treatments and they've kind of reached that point where they're very highly skilled and very well experienced.  And then there's others who are mum and dad who've just had a recent diagnosis for their child, they've gone searching on the internet, they can't find information, they don't have a patient organisation to rely on so they're going to make one themselves.  This happens all the time in the rare disease field.  There are 11,000 different rare conditions and there's not a group for all of them so mum and dad will often start something themselves and then in lots of cases want to do some research, they want to answer some of these questions.  So, you know, they're really starting from a very different beginning stage here where they've going to need some help, and sometimes the best help comes from their peers, it comes from other patient groups.  So that's in a nutshell what it's about; it's about providing opportunity for patient groups to showcase their great ideas, build partnerships and take research forward.   Rona: The only thing just to add there is I think, although rare diseases are individually rare, collectively, as Jo said, they're quite common, there's 11,000 rare diseases, and often, although they all have distinct features, there are common threads through rare diseases in terms of maybe symptoms that patients experience or challenges that their rare disease brings.  So, for example, you may have symptoms of pain or seizures that are common across many conditions, there may be educational needs that are threads going through.   And groups could work together maybe to answer a question that's relevant to a number of conditions and so bringing people together for that.  Or there may be another group that's already tried to answer that question in their condition and you can learn what worked, what didn't work.  I think that's the other thing, is there will be common threads that come through, and I think that would be a real strength of the network to draw those people together. Jo: I think as well, Mel, if we take this back to what we said right at the outset about optimising success for patients by bringing them into the conversation early, I think this platform provides the perfect opportunity to do that.  So we're moving away from, we're really turning research on its head, moving away from it being a researcher-led activity where they decide on the idea and the research concept and bring patients in at different points along that research journey and instead starting with the patient's idea in the first place.  It can only be a better system for all because it improves efficiency, it improves potentially the long-term outputs and, most importantly, outcomes for patients.  Mel: We were that family, that mum and dad setting up the charity a year and a half ago for the ultra-rare disease that our children had.  I think, you know, the match-making opportunities that are here are fantastic because finding yourself in that position is incredibly isolating.  And not only the matchmaking opportunities with the researchers but, as you were saying, Rona, as well with similar diseases; there's so much to learn from other diseases that may have, I don't know, a similar phenotype in the cells or similar symptoms.  That's what we found from connecting with these other rare conditions.  So, for us it's lysosomal storage diseases, we've now got the opportunity potentially to piggyback on drugs better used for their diseases for our own ultra rare condition, you know, where for us to run a full-on clinical trial by ourselves with a new drug, I mean, we just wouldn't have,  there's no funding, there's not enough interest.  So, I think the opportunities that lie in this network are really, really exciting.  Jo, can you tell me a bit more about who can join the research network?  Jo: So anyone with a rare disease research interest. That's everybody from individuals affected themselves, their family members, their caregivers, the patient organisations, that support them, and then, you know, all sorts of rare disease professional researchers.  So, we're looking for PhD students who are looking for their first exciting project to undertake, have they taken a look at the Rare Disease Research Network to see if there's any ideas that might pique their interest.  We're looking for established researchers, medical professionals who are undertaking clinical research but also I think, importantly, companies.   You know, we hear more and more about concepts like drug repurposing for rare diseases where we're looking at the opportunities for taking drugs that already exist and have been proven safe to be redeployed to other rare diseases. It's quicker, it's more efficient, it's cheaper, so does it open up opportunities for companies that are using that technique to get involved.  And also pharma companies.  This platform is not all going to be about finding cures and treatments but it certainly will be a priority for some groups.  So we really are welcoming everyone with an interest in rare disease research to get involved, be part of the network, collaborate, help where you can. Rona: And also, as we've said before, once you've got that level of engagement and the patients leading these initiatives we've found, certainly with our group, the patients are much more willing to, say, find the MRI scans for the scientists, to have a blood sample done, to have skin fibroblasts taken.  If they know and they understand and they're driven and, as you said, the research idea has come from them as a patient group it certainly increases the chance of them being fully involved in the project from the start to the finish.  And all these things are imperative to understanding rare conditions because without researchers having the opportunity to look at these various samples you're not going to stand much of a chance of finding a treatment.  Jo: And we want the opportunity to upskill patients as well.  I think there are many people out there with great ideas who haven't yet found the confidence to promote those ideas because they're not quite sure of what the research journey looks like or what it might entail or whether they've got the right skills.  But I think by joining the platform and almost kind of watching how other people are managing these things and utilising the resources and the mentoring I do really hope that will build that confidence and those skills sets in people so that they can engage.  Rona: Yeah, just to add to that, I don't think it's just upskilling patients and patient groups, I think it's upskilling everybody involved in rare disease research.  This is quite a different way of approaching research, it's something that maybe academics may feel a little bit uncomfortable with, it's not how it's normally done, so I think there's a whole learning process.  And the aim is that this RDR network will evolve and will develop and the direction it goes will be driven by the community that are engaging with it.  So I think it's a really exciting time just as we're coming up to launch to see where this goes.  Jo: Mel, you've been involved in this project, it would be really interesting actually to hear from you. I was just thinking, as part of the co-creation community we had 25 individuals from the rare disease community who built this platform from scratch with us; Rona and I might have set out all the vision for how we wanted the platform to be or what we thought might be a good idea but ultimately it was the community who decided and they literally have fact-checked and cross-referenced every word that's gone on the platform. What has that experience been like for you as a patient representative?  Mel: I think it's been really welcome to see a network that is truly putting patients at the centre of everything.  So, from the very beginning foundations you have the rare disease community involved which is exactly what you're trying to create through your network.  So, I think it's been very welcome to be involved in the project and I also think that hopefully it will sort of be self-perpetuating that this will start to press a reset button on how we think about rare conditions and how it needs to be a more equitable field with patients.  Because I think, as you've both alluded to, while some clinicians and researchers are very onboard with this, for others it's a new concept that they still need to potentially adjust to or get their head round because it is a different way of thinking.  But in rare disease, well, in any condition really but particularly rare disease because there's so few experiences to draw on, I think that patients are vital to moving forward and to making that change so that diseases and conditions that have previously had no treatment, like, hopefully this way of thinking can expedite those treatments because, well, as a rare disease representative myself for our community that's one of our biggest drivers.  We're dealing with a condition that's progressive that affects most of our community's children; that is what we want, we want treatment, we want something that can stabilise the conditions.  You know, you can have researchers doing random projects that would make no difference to the final outcome of patients but if researchers know it's a priority of this particular group, hopefully that can channel in their focus and get the outcomes that the patients want in a more timely collaborative way.  So, I am a huge advocate for what you're doing, I think it's an incredible initiative.  Is there anything either of you would like to add to that? Rona: Rare disease disproportionately affects children and young people.  So, 7 out of 10 rare diseases develop in childhood and at the moment the Rare Disease Research Network hasn't really got a forum for including children and young people, and really that's partly because, and Jo can speak much more eloquently to this with her experience.  Actually, we didn't do that at the start because we feel that this is actually a discreet piece of work that really needs to be done in collaboration with children and young people to make sure that it's done well so that they can engage in the platform. So, Jo, I don't know if you want to talk about how we're hoping to take this forward.  Jo: Yeah, so we're busy developing a project plan at the moment which we're hoping to get funding for to work over eighteen months with a team of young adults with rare conditions, probably from our Unique Feet community and keep it local because we already have a good relationship with them and they have our trust.  But the idea would be to work with lots of other young people's forums.  So there's already ones established in and around our area, such as Pedal, which works with really small children, and there's also groups that are set up for young people with cancer.  So we've already had lots of great conversations with them about how we can work with them, how they can help us sense-check our project, and then in return we can help them better understand research and their ability to be involved in that.  But ultimately by the end we want to run focus groups, we want to develop some peer mentors within our community, so young adults who've, you know, perhaps come out the other end of a period of transition into adulthood who can support other young people with rare diseases to also become researchers, to come up with their own ideas and their own questions, and to sense-check projects that come through the platform.  So it's a really exciting opportunity to truly involve the people who are affected most by rare conditions but we know through our My Story, My Way project that this has to be done gently, carefully, given time and done really thoughtfully.  So that's our next step and we hope to be able to share those learnings with people so that it can be done elsewhere.  Mel: And do you see the network also working with children with learning differences? Jo: Absolutely.  We'll invest a lot of time and energy in ensuring that materials are accessible, inclusive and suitable for the community that we're working with.  Mel: So looking to the future, how do you think, Rona, can patient-led research help to shape the future landscape?  Rona: So I think, Jo used the term earlier, kind of this is really turning research on its head, so it's really putting patients right at the centre of research, so it just makes sure that it's absolutely driven by what matters to them to get the outcomes that matter.  And, again, it's just got all that benefit of efficiency and really answering those questions that matter.  Mel: And, Jo, do you think this could lead to more collaborative partnership, for example, between industry and academia, potentially leading to quicker clinical advancement? Jo: I would absolutely like to think so.  You know, as CamRARE we run a companies forum which is a roundtable meeting for pharma and biotech companies and other organisations like Genomics England who are involved in the rare disease therapeutic space and diagnostics, and I think one thing that I find really heart-warming about those meetings is that, you know, different companies are able to sit around a table as competitors but with a very open mind to addressing the barriers and the bottlenecks that prevent them from getting drugs to patients.  Because of course it's not just the research journey that's a challenge, it's the regulatory side of things at the end of that journey; just because you've created a great drug it doesn't matter in the end if it doesn't get to the patient.  So, you know, access is critical and involving patients at the earliest possible moment to ensure that that treatment gets through to the regulators and gets access to patients is the only way forward.  We had a recent companies forum meeting where we were exploring health-related patient reported outcome measures, or PROMs, and we had a speaker from NICE who's the regulatory body, we had a speaker from Sheffield University who was talking as an academic about developing PROMs for industry and for patient groups and we had Emily Reuben, the CEO of Duchenne UK, and we had an amazing discussion about the importance of involving the patient community from the outset.  And the academic explained that developing a PROM for Duchenne UK had taken them two years and it had taken them that length of time because they'd followed this careful thoughtful pathway of making sure that they didn't assume anything about what matters to patients.  But that of course, as we said earlier, involves time, it involves financial commitment, it involves resources and the right attitude, but I do think that a platform like the Rare Disease Research Network can really try to harness all of those things by bringing the right people together – industry, academia and patients – to work together equitably. Mel: And with the network do you think you'll be getting the regulators in at that initial stage as well so that, like you said, the patients can gain access while we're dealing with their priorities, the regulators are informed at the very earliest stages so that we know the process that's being followed will ultimately lead to patients gaining access to the relevant therapies?  Jo: Yes, I think this is really important, and there's actually, we've got a section on the new platform which really talks to each of the different stakeholders.  ‘What's in this for me?'  ‘Why is it important for you to be here and to join?'  And one part of that is funders and that includes the regulatory bodies.  And at the next companies forum meeting we're actually going to be bringing the Rare Disease Research Network Platform and its potential to the companies forum meeting and we'll have regulators involved in that.  So, you know, we are constantly talking to people about why it's important for them all to be involved and all to see what matters. I think I'd like to advocate for an extra letter at the end of PPIEP - if we could squeeze a D in there at the end too.  So over time that terminology has expanded to be Public Patient Involvement Engagement and Participation, which was added I think this year, but it would be lovely to have the D on the end and to include ‘Driven' because I think what's really important about this platform is that it's not just engagement and involvement, it's not just participation, it's initiated by and driven by patients. Mel: So I think we'll wrap here.  Thank you to our guests, Jo Balfour and Dr Rona Smith, for joining me today as we discuss the role of patients in setting research agendas.  If you'd like to hear more like this, please subscribe to Behind the Genes on your favourite podcast app.  Thank you for listening.  I've been your host, Mel Dixon, and this podcast was edited by Bill Griffin at Ventoux Digital and produced by Naimah Callachand. 

Harsh Beniwal born in New Delhi is an Indian YouTuber with over 16M+ subscribers. He is often referred to as one of the OG YouTubers of India, as he was one of the first YouTubers in India who started making comedy sketch videos and later began creating long-form videos on YouTube. He made his film debut in Student of the Year 2. He also acted in web series such as Campus Diaries, and his new web series Heartbeats is streaming now. In this episode, Vinamre and Harsh talk about: - How his life has changed after becoming famous and Crazy car culture in Gurgaon - Balancing work and love, and why taking a break is important - The shift from YouTube to OTT platforms, preparations for his role in his upcoming series - Playing videos games like RDR 2 and GTA V, and weird Instagram algorithm - His experience of collaborating with CarryMinati on “MrBeast” parody video. Don't miss this episode to see Harsh Beniwal in his most genuine, unfiltered form. Timestamps: 00:00 - Introduction 0:55 - Beef with Ajaz Khan 2:53 - Getting fame for the first time 4:51 - How his family life has changed 8:12 - Crazy Car rides in Gurgaon 12:12 - Maturing at the right age 14:12 - Balancing work and love 16:20 - Behen-bhai content on YouTube 20:05 - Shooting “MrBeast” Parody Video with Carryminati 23:00 - Shifting from YouTube to OTT 29:15 - Adapting UP dialect for the series 33:36 - Taking a break from work is important 36:50 - Playing video games; RDR 2 and GTA V 46:54 - His most impulsive buy and VR experience 49:59 - Working with Ananya Pandey and Tiger Shroff 51:35 - Meeting Suresh Raina 52:55 - His lowest point in life 54:34 - Why the term “Bhaichara” is Dangerous 58:04 - The Plot of his series “Heartbeats” 1:00:05 - Weird Instagram reels and algorithm 1:06:35 - His favorite countries to visit 1:10:43 - Conclusion ==================================================================== This is the official channel for Dostcast, a podcast by Vinamre Kasanaa. Connect with me LinkedIn: https://www.linkedin.com/in/vinamre-kasanaa-b8524496/ Instagram: https://www.instagram.com/vinamrekasanaa/ Twitter: https://twitter.com/VinamreKasanaa Dostcast on Instagram: https://www.instagram.com/dostcast/ Dostcast on Twitter: https://twitter.com/dostcast Dostcast on Facebook: https://www.facebook.com/profile.php?id=61557567524054 ==================================================================== Contact Us For business inquiries: dostcast@egiplay.com

The gang comes together to discuss to preview UFC 309. First, they talk about the election and the impending doom we all face. They then talk about the last two UFC fight cards that included big wins for Prates, RDR, Blanchfield and Moreno. The gang then talks about this weekend's Jake Paul v. Mike Tyson freak show fight. They talk about Jon Jones trolling the world with his Aspinall comments before making their picks for UFC 309. All that and another edition of "Stuff We Like."

On Episode 3,512, the guys previewed the UFC card, went over all the latest news and then talked to Rich Franklin. They asked him about ONE championship but also got his take on RDR coming to UFC, Cris Cyborg one day possibly going for another belt and Mike Tyson vs Jake Paul.

محتويات الحلقة 00:01:54 موضوع ساخن ردود الفعل ضد Sweet baby تصريح يوبيسوفت عن مستقبلها سوبيسوفت تعترف ضعف اداء Star Wars Outlaws تصرفات جيف كيلي وجوائز السنة بوكيمون قو في السعودية وسرقة معلومات اللعبة مبيعات Detroit: Become Human الاعلان عن جزء ثاني للعبة Alien: Isolation استوديو 343 يغير اسمه الكويت تمنع Call Of Duty الجديدة مبيعات It Takes Two مبيعات Resident Evil 4 مبيعات Silent Hill 2 Remake 00:39:42 وش لعبنا 00:39:46 لعبة Silent Hill 2 Remake 00:56:37 لعبة The First Berserker: Khazan 01:04:18 آخبار سريعة تأسيس استوديو من مطوري RDR وماريو تطوير لعبة عن Avatar the Last Airbender اعادة تطوير مسلسل عن God of War كونتي سوف تطلق محرك Unity 6 لعبة جديدة من Remedy عرض Xbox Tokyo Game Show تشويقي عن Arma 4 سوني سوف تقوم بحفلة موسيقية تطوير لعبة Death Note لعبة  Destiny: Rising للهواتف 01:04:00 تعليقات المستمعين الحضور: خالد ٬ نواف

Siga o XdC no Bluesky | Siga o XdC no Threads Neste episódio de O X do Controle News, PH Lutti Lippe e Guilherme Dias reportam e discutem as principais notícias da semana no mundo dos games.  Em pauta: foram revelados em um livro os bastidores do cancelamento de Titan, o projeto gigante da Blizzard dos quais os restos viraram Overwatch; os criadores de Mario + Rabbids e do primeiro Red Dead Redemption se uniram para fundar um estúdio; e o anime de Avatar vai ganhar um RPG de grande porte feito pela Saber Interactive. Tudo isso e mais um pouco você confere nesta edição! MARCAÇÕES DE TEMPO (0:00:00) - Abertura (0:07:56) - Projeto Titan, o “matador de WoW” que morreu e virou Overwatch (0:34:25) - Diretor de Mario + Rabbids e roteirista de RDR fundam estúdio (0:41:30) - Saber Interactive anuncia RPG de ação AAA no mundo do anime Avatar  (0:53:43) - Rapidinhas (0:59:08) - Encerramento Seja apoiador | YouTube | Twitter | Instagram | Tik Tok Nossas plataformas Contato: contato@xdocontrole.com CRÉDITOS: Apresentação: PH Lutti Lippe e Guilherme Dias Roteiro: PH Lutti Lippe Edição: Gabriel Sales Thumbnail: Lucas Ferreira

In this episode of RDR, Scott sits down with Penny Zenker, a world-renowned productivity expert and author of The Productivity Zone and The Reset Mindset. Penny shares her journey from experiencing a life-changing event at 19 to becoming a leading authority on focus and productivity.She introduces her "Reset Moments" framework, explaining how both big and small resets can help us reduce stress, boost productivity, and stay aligned with our goals. Penny also offers practical tips for business owners on prioritizing tasks, avoiding the pitfalls of multitasking, and creating habits that foster intentional leadership.Whether you're a small business owner or simply looking for ways to improve your focus, this episode is packed with actionable advice to help you reset, refocus, and lead with clarity. Tune in to learn how you can transform chaos into clarity with Penny's proven strategies!---Episode Markers:(0:00) - Introduction & Overview(1:00) - Reflecting on Accomplishments(3:00) - Journaling and Self-Awareness(4:45) - Introduction to Reset Moments(7:45) - Daily Reset Moments & Their Importance(8:30) - Perspective Shifts and Fear Cues(9:50) - The Challenges of Multitasking(12:00) - The Importance of Presence(13:30) - Reset Moments for Small Business Owners(16:30) - Prioritization and False Urgencies(17:00) - Practical Hacks(21:20) - The 80/20 Rule for Prioritization(22:50) - Creating Consistency with Reset Moments(24:00) - The Three Gatekeepers: Rules, Filters, and Environment(30:00) - Building a Team Reset Culture(34:00) - Strengths & Weaknesses(35:20) - The Power of Language and Reset Moments---Scott Grates Links:Referrals Done Right Book Pre Sales - https://www.referralsdonerightbook.comReferrals Done Right FB Group - https://www.facebook.com/groups/296359076662332Insurance Agency Optimization - https://www.agencyoptimization.comScott Grates Website - https://www.scottgrates.comLove Living Local  - https://www.instagram.com/lovelivinglocal315Scott's FB - https://www.facebook.com/scott.grates.1Instagram - https://www.instagram.com/scottgratesPenny Zenker's Links:The Reset Mindset Book - https://pennyzenker360.com/the-reset-mindsetPenny's Website - https://pennyzenker360.comFB - https://www.facebook.com/PennyzPerspective---The Referrals Done Right Podcast is sharing the secrets to creating infinite opportunities to grow your small business. Hosted by Scott Grates.

This episode of RDR is the 2nd half of a snippet from Scott's appearance on the Positive Blatherings Podcast hosted by Scott Fitzgerald. Scott has been working in video production for over 25 years, radio for 8 years and in and out of bands and recording studios since graduating from high school. In 2018, Scott became the proud co-owner of ROC Vox Recording & Production.---Episode Markers:---Scott Grates Links:Referrals Done Right Book Pre Sales - https://www.referralsdonerightbook.comReferrals Done Right FB Group - https://www.facebook.com/groups/296359076662332Insurance Agency Optimization - https://www.agencyoptimization.comScott Grates Website - https://www.scottgrates.comLove Living Local  - https://www.instagram.com/lovelivinglocal315Scott's FB - https://www.facebook.com/scott.grates.1Instagram - https://www.instagram.com/scottgratesPositive Blatherings' Links:Roc Vox Website - https://rocvox.comFB - https://www.facebook.com/ROCVoxRecording---The Referrals Done Right Podcast is sharing the secrets to creating infinite opportunities to grow your small business. Hosted by Scott Grates.

This episode of RDR is a snippet from Scott's appearance on the Positive Blatherings Podcast hosted by Scott Fitzgerald. Scott has been working in video production for over 25 years, radio for 8 years and in and out of bands and recording studios since graduating from high school. In 2018, Scott became the proud co-owner of ROC Vox Recording & Production.---Episode Markers:---Scott Grates Links:Referrals Done Right Book Pre Sales - https://www.referralsdonerightbook.comReferrals Done Right FB Group - https://www.facebook.com/groups/296359076662332Insurance Agency Optimization - https://www.agencyoptimization.comScott Grates Website - https://www.scottgrates.comLove Living Local  - https://www.instagram.com/lovelivinglocal315Scott's FB - https://www.facebook.com/scott.grates.1Instagram - https://www.instagram.com/scottgratesPositive Blatherings' Links:Roc Vox Website - https://rocvox.comFB - https://www.facebook.com/ROCVoxRecording---The Referrals Done Right Podcast is sharing the secrets to creating infinite opportunities to grow your small business. Hosted by Scott Grates.

This episode of RDR is the second half of a conversation between Scott and Stephen Turnbull, owner of T5 Insurance Services & cohost of The Scratch Agency Podcast.---Episode Markers:(0:00) - Episode Intro(1:35) - Show Start(2:30) - Social Strategy(4:45) - If You're Not Unique, You're Weak(6:50) - Out of the Box Thinking(8:10) - Value of Working with Schools(9:00) - Attaching Yourself to Organizations(10:55) - Yankee Stadium Trip(12:30) - Starting the Utica BNI Chapter(15:30) - Becoming a Connector(17:10) - Just Ask---Scott Grates Links:Referrals Done Right Book Pre Sales - https://www.referralsdonerightbook.comReferrals Done Right FB Group - https://www.facebook.com/groups/296359076662332Insurance Agency Optimization - https://www.agencyoptimization.comScott Grates Website - https://www.scottgrates.comLove Living Local  - https://www.instagram.com/lovelivinglocal315Scott's FB - https://www.facebook.com/scott.grates.1Instagram - https://www.instagram.com/scottgratesStephen Turnbull's Links:T5 Website - https://www.t5insurance.comT5 FB - https://www.facebook.com/t5insuranceT5 IG - https://www.instagram.com/t5insuranceStephen FB - https://www.facebook.com/stephen.turnbull.31Stephen IG - https://www.instagram.com/insureguy315/Podcast Website - https://scratchagencypodcast.comScratch Agency Podcast - https://podcasts.apple.com/us/podcast/the-scratch-agency-podcast/id1653015248---The Referrals Done Right Podcast is sharing the secrets to creating infinite opportunities to grow your small business. Hosted by Scott Grates.

This episode of RDR is the first part of a conversation between Scott and Stephen Turnbull, owner of T5 Insurance Services & cohost of The Scratch Agency Podcast.---Episode Markers:(0:00) - Episode Intro(1:35) - Show Start & Stephen's Background(4:20) - Branding New Agency(6:35) - Telling is Not Selling(7:50) - Knowing Somebody Who Does(10:50) - Talking Benefits(11:50) - Leading with Consequences(13:05) - Using Power Words(15:25) - Referral Strategy(17:00) - Leads Aren't For Everyone(19:05) - Unique Gift Giving---Scott Grates Links:Referrals Done Right Book Pre Sales - https://www.referralsdonerightbook.comReferrals Done Right FB Group - https://www.facebook.com/groups/296359076662332Insurance Agency Optimization - https://www.agencyoptimization.comScott Grates Website - https://www.scottgrates.comLove Living Local  - https://www.instagram.com/lovelivinglocal315Scott's FB - https://www.facebook.com/scott.grates.1Instagram - https://www.instagram.com/scottgratesStephen Turnbull's Links:T5 Website - https://www.t5insurance.comT5 FB - https://www.facebook.com/t5insuranceT5 IG - https://www.instagram.com/t5insuranceStephen FB - https://www.facebook.com/stephen.turnbull.31Stephen IG - https://www.instagram.com/insureguy315/Podcast Website - https://scratchagencypodcast.comScratch Agency Podcast - https://podcasts.apple.com/us/podcast/the-scratch-agency-podcast/id1653015248---The Referrals Done Right Podcast is sharing the secrets to creating infinite opportunities to grow your small business. Hosted by Scott Grates.

This episode of RDR is the second half of a conversation between Scott and agent Katie Myers from Janesville, WI. We discuss building community from scratch, starting in a new area, serving others & constantly staying top of mind.---Episode Markers:(0:00) - Episode Intro(1:30) - Show Start(1:50) - Mayor without the Politics(3:30) - Superconnectors(4:20) - Patience & Conistency(7:30) - Advice For Starting(9:50) - Context From Social Media(12:10) - Off the Beaten Career Path Podcast(14:30) - Best Stories(16:55) - Saying No?(18:40) - Future Plans(20:50) - Don't Think Anything is Beneath You(22:55) - TikTok & Meeting People Where They Are---Scott Grates Links:Referrals Done Right Book Pre Sales - https://www.referralsdonerightbook.comReferrals Done Right FB Group - https://www.facebook.com/groups/296359076662332Insurance Agency Optimization - https://www.agencyoptimization.comScott Grates Website - https://www.scottgrates.comLove Living Local  - https://www.instagram.com/lovelivinglocal315Scott's FB - https://www.facebook.com/scott.grates.1Instagram - https://www.instagram.com/scottgratesKatie Myers' Links:Agency FB - https://www.facebook.com/katiemyersjanesvillePodcast - https://podcasts.apple.com/us/podcast/off-the-beaten-career-path/id1702352850TikTok- https://www.tiktok.com/@the_katie_myers?_t=8pSvhXKhDWl&_r=1---The Referrals Done Right Podcast is sharing the secrets to creating infinite opportunities to grow your small business. Hosted by Scott Grates.

This episode of RDR is the first part of a conversation between Scott and agent Katie Myers from Janesville, WI. We discuss building community from scratch, starting in a new area, serving others & constantly staying top of mind.---Episode Markers:(0:00) - Episode Intro(1:40) - Show Start(2:20) - Starting in a New Town(4:00) - Finding Opportunities(6:00) - Building Women's Networking Group(8:30) - Advice on Networking & Easy Wins(9:30) - Referral Based Business(10:50) - Powers of Google Reviews(12:00) - Referral Strategies(15:00) - Creating Memorable Customer Experiences(17:15) - Maintaining Strong Relationships(19:00) - Facebook(20:25) - Types of Content---Scott Grates Links:Referrals Done Right Book Pre Sales - https://www.referralsdonerightbook.comReferrals Done Right FB Group - https://www.facebook.com/groups/296359076662332Insurance Agency Optimization - https://www.agencyoptimization.comScott Grates Website - https://www.scottgrates.comLove Living Local  - https://www.instagram.com/lovelivinglocal315Scott's FB - https://www.facebook.com/scott.grates.1Instagram - https://www.instagram.com/scottgratesKatie Myers' Links:Agency FB - https://www.facebook.com/katiemyersjanesvillePodcast - https://podcasts.apple.com/us/podcast/off-the-beaten-career-path/id1702352850---The Referrals Done Right Podcast is sharing the secrets to creating infinite opportunities to grow your small business. Hosted by Scott Grates.

This episode of RDR is the second part of a conversation between Scott and Tyler Jensen, founder of Insurarisk University. Tyler is a speaker on top performance, a certified insurance counselor & an optimist coach.---Episode Markers:(0:00) - Episode Intro(1:50) - Show Start(2:30) - Where to Start?(5:20) - Three Reasons People Don't Buy(6:45) - Mid Way Ask & Soft Close(7:45) - Customer Isn't Ready to Give Referral Scenario---Scott Grates Links:Referrals Done Right Book Pre Sales - https://www.referralsdonerightbook.comReferrals Done Right FB Group - https://www.facebook.com/groups/296359076662332Insurance Agency Optimization - https://www.agencyoptimization.comScott Grates Website - https://www.scottgrates.comLove Living Local  - https://www.instagram.com/lovelivinglocal315Scott's FB - https://www.facebook.com/scott.grates.1Instagram - https://www.instagram.com/scottgratesTyler Jensen's Links:Tyler's Website - https://www.tylerjjensen.comInsurarisk Website- https://www.insurariskuniversity.com/Instagram - https://www.instagram.com/tyler_j_jensenFacebook - https://www.facebook.com/profile.php?id=61558802128625Linkedin - https://www.linkedin.com/in/tyler-jensenYouTube - https://www.youtube.com/channel/UC5IDcFyXDaIs1MxMNJYDB8w---The Referrals Done Right Podcast is sharing the secrets to creating infinite opportunities to grow your small business. Hosted by Scott Grates.

This episode of RDR is the first part of a conversation between Scott and Tyler Jensen, founder of Insurarisk University. Tyler is a speaker on top performance, a certified insurance counselor & an optimist coach.---Episode Markers:(0:00) - Episode Intro(1:30) - Show Start(1:55) - What is an Optimist Coach?(4:00) - Strategies to Stay Optimistic(6:45) - Value & Experience(10:15) - Embedding in Onboarding Process(12:15) - Don't Trust Your Memory & Being Seen(13:15) - Employee Experience(13:45) - Becoming Referable & Culture(15:00) - Key Elements to Creating Culture(17:15) - Craving to be Recognized(18:30) - Empowering Team Members & Integrity(20:15) - Insurarisk University & Connecting with Tyler---Scott Grates Links:Referrals Done Right Book Pre Sales - https://www.referralsdonerightbook.comReferrals Done Right FB Group - https://www.facebook.com/groups/296359076662332Insurance Agency Optimization - https://www.agencyoptimization.comScott Grates Website - https://www.scottgrates.comLove Living Local  - https://www.instagram.com/lovelivinglocal315Scott's FB - https://www.facebook.com/scott.grates.1Instagram - https://www.instagram.com/scottgratesTyler Jensen's Links:Tyler's Website - https://www.tylerjjensen.comInsurarisk Website- https://www.insurariskuniversity.com/Instagram - https://www.instagram.com/tyler_j_jensenFacebook - https://www.facebook.com/profile.php?id=61558802128625Linkedin - https://www.linkedin.com/in/tyler-jensenYouTube - https://www.youtube.com/channel/UC5IDcFyXDaIs1MxMNJYDB8w---The Referrals Done Right Podcast is sharing the secrets to creating infinite opportunities to grow your small business. Hosted by Scott Grates.

This episode of RDR is the second half of a conversation between Scott and Michael Weaver, Founder of Weaver Sales Academy. Michael is a speaker, author, sales trainer and the co host of the Insurance Buzz Podcast. We dive into centers of influence, referral partners, social media strategy & more.---Episode Markers:(0:00) - Episode Intro(1:55) - Show Start(2:30) - Centers of Influence & Referral Partners(3:15) - Why Refer to You? Integrity is Everything(7:30) - Different Tools For Engaging(8:00) - Jab Jab Jab Uppercut(9:05) - Social Media(10:30) - Approach to Building & Strengthening Relationships on Social(12:50) - Different Avenues of Your Brand(14:00) - Speaking Directly to Customer Pain Points(15:00) - Peeling Back the Layers & Asking Better Questions(18:00) - Strategies(20:50) - Personal Level on Social(22:15) - Becoming Your Own Media(27:00) - Michael's Book---Scott Grates Links:Referrals Done Right Book Pre Sales - https://www.referralsdonerightbook.comReferrals Done Right FB Group - https://www.facebook.com/groups/296359076662332Insurance Agency Optimization - https://www.agencyoptimization.comScott Grates Website - https://www.scottgrates.comLove Living Local  - https://www.instagram.com/lovelivinglocal315Scott's FB - https://www.facebook.com/scott.grates.1Instagram - https://www.instagram.com/scottgratesMichael Weaver's Links:Website - https://www.weaversa.comBook - https://www.quote3book.comThe Insurance Buzz Podcast - https://podcasts.apple.com/us/podcast/the-insurance-buzz/id1606064185Linkedin - https://www.linkedin.com/in/michaelweaverwsaFacebook - https://www.facebook.com/themichaelweaver---The Referrals Done Right Podcast is sharing the secrets to creating infinite opportunities to grow your small business. Hosted by Scott Grates.

On this episode of RDR, Scott is joined by Michael Weaver, Founder of Weaver Sales Academy. Michael is a speaker, author, sales trainer and the co host of the Insurance Buzz Podcast---Episode Markers:(0:00) - Episode Intro(1:45) - Show Start(3:30) - Costa Rica Story(7:00) - New Customers(10:20) - Warm Handoffs & Building Rapport(12:30) - Retention(13:20) - Face to Face---Scott Grates Links:Referrals Done Right Book Pre Sales - https://www.referralsdonerightbook.comReferrals Done Right FB Group - https://www.facebook.com/groups/296359076662332Insurance Agency Optimization - https://www.agencyoptimization.comScott Grates Website - https://www.scottgrates.comLove Living Local  - https://www.instagram.com/lovelivinglocal315Scott's FB - https://www.facebook.com/scott.grates.1Instagram - https://www.instagram.com/scottgratesMichael Weaver's Links:Website - https://www.weaversa.comThe Insurance Buzz Podcast - https://podcasts.apple.com/us/podcast/the-insurance-buzz/id1606064185Linkedin - https://www.linkedin.com/in/michaelweaverwsaFacebook - https://www.facebook.com/themichaelweaver---The Referrals Done Right Podcast is sharing the secrets to creating infinite opportunities to grow your small business. Hosted by Scott Grates.

It's time once again to chat about last wednesday's best books! This week we drink some hypnotic energy drinks and play RDR, discuss the ethics of destroying the world, and ask the age old question: "what's going on with that horse?"    Pull List (with spoiler time stamps): 00:11:02 - Gotham City Sirens #1 00:22:17 - Uncanny X-Men #1 00:39:01 - Power Fantasy #1 00:54:10 - Scarlett #3 Support Tales From The Short Box by joining our Patreon! patreon.com/BraveNewWorldsComics  

In this episode of Referrals Done Right, Scott shares his advice for people who are just getting started from scratch with referrals. Listen for the five steps to start your journey into the RDR system.---Links:Insurance Agency Optimization - https://www.agencyoptimization.com/Love Living Local  - https://www.instagram.com/lovelivinglocal315/Scott's FB - https://www.facebook.com/scott.grates.1Essential F-Words Website -  https://www.essentialfwords.com/Essential F-Words Amazon - https://www.amazon.com/Essential-F-Words-Teens-Things-Graduation/dp/B0BW2MGVJW---The Referrals Done Right Podcast is sharing the secrets to creating infinite opportunities to grow your small business.

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Join the Patreon! https://www.patreon.com/theleoanddannyshow?fan_landing=true Support our Sponsors! ▶ Raycon : https://www.buyraycon.com/lds Use code LDS and get 20% off! ▶ Meundies : https://www.meundies.com/leodanny Get 20% off and Free Shipping! with our link! Support our Guests! RDR's INSTAGRAM ▶ https://www.instagram.com/ratdick_ralph/?hl=en RDR's Channel ▶ https://www.youtube.com/@RatdickRalph RDR's Trovo ▶ @ratdickralph Support the Podcast! Leo's Merch ▶ https://merchyy.com/collections/leo-dottavio Leo's Patreon ▶ https://www.patreon.com/user?u=26041367 Danny's Patreon ▶ https://www.patreon.com/DannyMullen Subscribe to the Crew! Leo's Channel ▶ https://www.youtube.com/channel/UCTTcsKnU0T_g7sLNvwVzpDg Danny's Channel ▶ https://www.youtube.com/channel/UCnyxus3H0_-F8Q6gQTkg41g Austin's Channel: ▶ https://www.youtube.com/channel/UCDGGwNDa3gGXX11o2WT2a-A Austin's Kick ▶ https://kick.com/archangelaustin Dino's Chanel ▶ https://www.youtube.com/channel/UCVbGgB-fCEUp9WEMiI0BeHg Follow the Crew! Leo's IG ▶ https://www.instagram.com/leofdot/ Austin's IG ▶ https://www.instagram.com/austin.schlosser/ Danny's IG ▶https://www.instagram.com/dannymullen/ Dino's Instagram ▶ https://www.instagram.com/big.d.dino/?hl=en Leo's Twitter: @Leodottavio Danny's Twitter: @DannyMullenfts

Join the Patreon! https://www.patreon.com/theleoanddannyshow?fan_landing=true Support our Sponsors! ▶ Prize Picks : https://www.prizepicks.com/lds Get your first $100 deposit matched with Our Code : LDS Support our Guests! ▶ Shipstation : https://www.shipstation.com/ Get 60 days FREE! USE CODE: LDS RDR's INSTAGRAM ▶ https://www.instagram.com/ratdick_ralph/?hl=en RDR's Channel ▶ https://www.youtube.com/@RatdickRalph RDR's Trovo ▶ @ratdickralph Support the Podcast! Leo's Merch ▶ https://merchyy.com/collections/leo-dottavio Leo's Patreon ▶ https://www.patreon.com/user?u=26041367 Danny's Patreon ▶ https://www.patreon.com/DannyMullen Subscribe to the Crew! Leo's Channel ▶ https://www.youtube.com/channel/UCTTcsKnU0T_g7sLNvwVzpDg Danny's Channel ▶ https://www.youtube.com/channel/UCnyxus3H0_-F8Q6gQTkg41g Austin's Channel: ▶ https://www.youtube.com/channel/UCDGGwNDa3gGXX11o2WT2a-A Austin's Kick ▶ https://kick.com/archangelaustin Dino's Chanel ▶ https://www.youtube.com/channel/UCVbGgB-fCEUp9WEMiI0BeHg Follow the Crew! Leo's IG ▶ https://www.instagram.com/leofdot/ Austin's IG ▶ https://www.instagram.com/austin.schlosser/ Danny's IG ▶https://www.instagram.com/dannymullen/ Dino's Instagram ▶ https://www.instagram.com/big.d.dino/?hl=en Leo's Twitter: @Leodottavio Danny's Twitter: @DannyMullenfts

Join the Patreon! https://www.patreon.com/theleoanddannyshow?fan_landing=true Support our Sponsors! ▶ Raycon : https://www.buyraycon.com/lds Use code LDS and get 20% off! Support our Guests! RDR's INSTAGRAM ▶ https://www.instagram.com/ratdick_ralph/?hl=en RDR's Channel ▶ https://www.youtube.com/@RatdickRalph RDR's Trovo ▶ @ratdickralph Support the Podcast! Leo's Merch ▶ https://merchyy.com/collections/leo-dottavio Leo's Patreon ▶ https://www.patreon.com/user?u=26041367 Danny's Patreon ▶ https://www.patreon.com/DannyMullen Subscribe to the Crew! Leo's Channel ▶ https://www.youtube.com/channel/UCTTcsKnU0T_g7sLNvwVzpDg Danny's Channel ▶ https://www.youtube.com/channel/UCnyxus3H0_-F8Q6gQTkg41g Austin's Channel: ▶ https://www.youtube.com/channel/UCDGGwNDa3gGXX11o2WT2a-A Austin's Kick ▶ https://kick.com/archangelaustin Dino's Chanel ▶ https://www.youtube.com/channel/UCVbGgB-fCEUp9WEMiI0BeHg Follow the Crew! Leo's IG ▶ https://www.instagram.com/leofdot/ Austin's IG ▶ https://www.instagram.com/austin.schlosser/ Danny's IG ▶https://www.instagram.com/dannymullen/ Dino's Instagram ▶ https://www.instagram.com/big.d.dino/?hl=en Leo's Twitter: @Leodottavio Danny's Twitter: @DannyMullenfts

MERCH IS HERE: https://storyofthefight.etsy.com Thank you so much ONE Championship for letting us use your footage! ATTRIBUTIONS SOURCE: https://www.youtube.com/@ONEChampionship CREATED BY: ONE Championship Link to full Video Episode: https://youtu.be/qbCpdLN0xMY ALERT: Next week you are welcome to join us LIVE on our YouTube Channel at 9am PST/11am CST if you wanna comment and laugh along with Will, Miro, and Rich! Otherwise, hit us up any way you like including by email to have your questions answered in our mailbag episode! Please leave a rating and a review along with a subscription, and check out our YouTube channel to like & subscribe! https://Instagram.com/StoryoftheFight https://Twitter.com/StoryoftheFight https://Twitch.tv/storyofthefight TikTok: @StoryoftheFight Facebook Group: https://m.facebook.com/home.php#!/groups/903248290491045?group_view_referrer=search --- Timestamps: 0:00 - Intro 00:15 - Malykhin vs RDR 2 12:29 - Tang Kai vs Thanh Le 2 16:27 - Pacio vs Brooks 2 23:38 - Aliakbari vs Bhullar 28:23 - Kuzmin vs Sayik 33:56 - Next Week Preview #ONE166 #AnatolyMalykhin #ONEchampionship

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Support our Sponsors ▶ Prize Picks : https://www.prizepicks.com/lds Get your first $100 deposit matched with Our Code : LDS ▶ Shipstation : https://www.shipstation.com/ Get 60 days FREE! USE CODE: LDS Join the Patreon! https://www.patreon.com/theleoanddannyshow?fan_landing=true Support our Guests! RDR's INSTAGRAM ▶ https://www.instagram.com/ratdick_ralph/?hl=en RDR's Channel ▶ https://www.youtube.com/@RatdickRalph Support the Podcast! Leo's Merch ▶ https://merchyy.com/collections/leo-dottavio Leo's Patreon ▶ https://www.patreon.com/user?u=26041367 Danny's Patreon ▶ https://www.patreon.com/DannyMullen Subscribe to the Crew! Leo's Channel ▶ https://www.youtube.com/channel/UCTTcsKnU0T_g7sLNvwVzpDg Danny's Channel ▶ https://www.youtube.com/channel/UCnyxus3H0_-F8Q6gQTkg41g Austin's Channel: ▶ https://www.youtube.com/channel/UCDGGwNDa3gGXX11o2WT2a-A Austin's Kick ▶ https://kick.com/archangelaustin Dino's Chanel ▶ https://www.youtube.com/channel/UCVbGgB-fCEUp9WEMiI0BeHg Follow the Crew! Leo's IG ▶ https://www.instagram.com/leofdot/ Austin's IG ▶ https://www.instagram.com/austin.schlosser/ Danny's IG ▶https://www.instagram.com/dannymullen/ Dino's Instagram ▶ https://www.instagram.com/big.d.dino/?hl=en Leo's Twitter: @Leodottavio Danny's Twitter: @DannyMullenfts

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Voilà près de 30 ans que Jean-Marie Liot photographie des bateaux de course ; 30 ans qu'il doute, qu'il hésite, et prend la mer ou les airs, ses boîtiers d'appareil photo à la main, se demandant si la lumière est bonne, si le cadrage convient, s'il n'a pas loupé une vague d'étrave qui explose ou un sillage qui fume. Un doute salvateur, capable de produire cette "plaque" déjà légendaire d'une meute de Class40 cavalant dans les embruns au reaching au départ de la Transat Jacques Vabre. - reprise partout, y compris dans Paris Match sur une double page. Car sous ses airs de jeune premier qui débute, Jean-Marie Liot est incontournable : Vendée Globe, Route du Rhum, Transat Jacques Vabre, Tour Voile, Normandy Channel Race, banques images... À 52 ans, s'il donne l'impression d'être motivé et impliqué comme au premier jour, il est de tous les grands rendez-vous. Pourtant, quand il se met à la photo au début des années 1990, c'est d'abord qu'il y voit un moyen d'assouvir sa passion de la mer et des bateaux, transmise par son père - d'ailleurs, il passera son PPV (diplôme de skipper pro) après son école de photo suivie à Paris. Il apprendra sur le tas ensuite, en s'inspirant de ses modèles Gilles Martin-Raget et Franco Pace, ouvrira une galerie au Crouesty, avant d'être aspiré par les compétitions. Sans oublier de se diversifier : qui sait, sur les pontons, que Jean-Marie Liot s'est aussi spécialisé dans la photo culinaire, une "discipline différente". Et l'on veut croire, en l'écoutant, que ça ne vaut pas une séance en mer, le plus beau studio photo du monde... Diffusé le 3 novembre 2023 Générique : In Closing – Days Past Post-production : Grégoire Levillain

Il fait penser à ces grands profs de fac qui vous marquent longtemps, ceux dont les cours magistraux se dégustent comme des spectacles, et dont vous savez, en sortant de l'amphi, que vous êtes moins bête que lorsque vous êtes rentré. Jean-Yves Bernot est de ceux-là : référence absolue de son domaine - la stratégie météo - et formidable pédagogue - il a écrit des dizaines de bouquins, que tous les coureurs ont dans leur bibliothèque. Il naît loin de la mer - pas très longtemps après la guerre même s'il ne veut pas dire son âge ! -, mais passe ses vacances en Bretagne. Ce sont les Glénans (l'école) qui l'embarqueront définitivement vers le vent et les vagues : après un bac + 5 en maths à Reims, il bifurque vers l'océanographie à Brest - mais l'appel de la course est le plus fort. Le Triangle Atlantique (1975), les courses du Rorc, la Solitaire du Figaro (1983) forgent le marin qui se retrouve très vite à la table à cartes, où il n'est pas manchot, à l'époque où le GPS n'est pas encore arrivé. Fort en équations, passionné de météo, il accompagne dans les années 1980 les débuts de MacSea (bientôt MaxSea), pionnier des logiciels de navigation. C'est là qu'il développe sa méthode, associant expérience maritime, climatologie, routage et - surtout - stratégie : son expertise est là, dans l'exercice de la prise de décision. Très vite, tout le monde s'arrache Bernot, devenu "le Sorcier" qui sait lire entre les isobares. Jeantot, Poupon, le Corum Sailing Team, le Pôle Finistère course au large, feront appel à lui. Le Rochelais (il s'y est installé en 1983) continue à naviguer sur The Race (2001) et la Volvo Ocean Race (2001-2002). Le tour du monde est son domaine : les participants au Vendée Globe se préparent avec lui ; MacArthur, Joyon, Gabart sont routés pour leurs records victorieux. Mais jamais il n'a renoncé à former les débutants et les amateurs, "ouvrir les portes" est un atavisme familial pour ce fils d'instit. Sur la Transat Jacques Vabre 2023, il route François Gabart et Tom Laperche, avant d'accompagner le second sur l'Arkea Ultim Challenge-Brest. Des heures à venir, derrière les écrans, à ausculter le ciel, l'océan et les cerveaux des marins. Diffusé le 20 octobre 2023 Générique : In Closing – Days Past Post-production : Grégoire Levillain

Sur le papier, la voie de Nicolas Lunven était toute tracée : avec un père participant à plusieurs reprises de la Course de l'Aurore, la filiation semblait évidente. Sauf que non : les exploits paternels datent d'avant sa naissance, en 1982, et il commence par des croisières familiales. Mais bon sang ne saurait mentir, et il embarque en course dès l'adolescence. Mais pas de formation en voile légère ni par la Mini Transat : Lulu, comme beaucoup l'appellent, fait ses armes en habitable, et en particulier sur le Tour Voile, auquel il participera 11 fois. En tentant sa chance lors du Challenge Esoir Crédit Agricole, c'est la révélation : le Figaro sera sa passion. Charles Caudrelier l'appelle pour prendre la barre de son Figaro en 2007, et il finit premier bizuth. Deux ans plus tard, il remporte la Solitaire, à 25 ans, au milieu des cadors de l'époque. Sa carrière est lancée : Solitaire, TFV, Sydney-Hobart, il enchaîne et s'autorise une pause en 2014, pour participer à la Volvo Ocean Race sur Mapfre. L'expérience est de courte durée, mais elle confirme que Nicolas Lunven entre désormais dans la catégorie des équipiers recherchés puisqu'il embarque sur l'Imoca Safran. Et s'il retourne en Figaro ensuite, c'est pour survoler la saison 2017 et entrer dans le club fermé des doubles vainqueurs de l'épreuve. Sa carrière s'accélère et le téléphone sonne : nouvelle Volvo Ocean Race sur Turn The Tide On Plastic, nouvelle saison en Imoca, avec PRB puis Initiatives-Coeur, pige chez Banque Pop pour remplacer Clarisse Crémer pendant sa grossesse, retour à The Ocean Race avec Malizia et, finalement, en septembre de cette année, il remplace Kevin Escoffier à la barre d'Holcim-PRB. Voilà comment, à 40 ans, on devient un candidat plus que sérieux au départ du prochain Vendée Globe. Avec rigueur, sérieux et discrétion. Mais ne vous fiez pas à sa réputation tranquille : derrière son regard clair, Lulu sait faire aller - très - vite les bateaux....  Diffusé le 6 octobre 2023 Générique : In Closing – Days Past Post-production : Grégoire Levillain

On l'avait un peu oublié, mais Benjamin Dutreux n'a que 33 ans. Et déjà, dans son sillage, Solitaire du Figaro, Transat Jacques Vabre, Route du Rhum, Vendée Globe et The Ocean Race... Après une brillante carrière dans la filière multicoque chez les jeunes et un premier job chez un constructeur de catas de sport, le voilà qui plonge dans le Figaro en 2015. Il n'a jamais couru en solitaire mais 4 saisons plus tard, il rentre dans le top 5 en 2018 pour sa dernière participation. Entre temps le virus du Vendée Globe l'a rattrapé : il part au Japon racheter le plan Farr de Kojiro Shiraishi en 2019 et se lance dans une campagne express : Transat Jacques Vabre à l'arrache et... plus aucune course pour cause de Covid, jusqu'au Défi Azimut 2020, sa première course en solo en Imoca, moins de 2 mois avant le départ. C'est mal connaître Benjamin Dutreux que de s'inquiéter pour lui. Il joue les premiers rôles sur son Imoca à dérives devant une meute de foilers dès le départ, ne cédant une incroyable 5e place que sur le tard pour se classer finalement 9e. Pas question de s'arrêter là : dans les mois qui suivent il enchaîne une nouvelle Transat Jacques Vabre avec Damien Seguin, participe à The Ocean Race Europe avec Team Germany tout en négociant l'ex 11th Hour Racing ! Puis il trouve un nouveau sponsor - Guyot Environnement -, le convainc de s'engager sur The Ocean Race en 2023, et participe à la Route du Rhum 2022, qu'il termine en 8e position. A peine le temps de souffler, et quelques semaines plus tard, départ d'Alicante avec une équipe qui a doublé de taille. Ce second tour du monde va s'avérer un long chemin de croix, avec un abandon sur délaminage du fond de coque après Le Cap, un démâtage après Recife, et un funeste refus de tribord au futur vainqueur à La Haye... Benjamin Dutreux en parle sans fioriture, grandi - lui comme son équipe - par l'expérience. Et en l'écoutant longuement, on comprend qu'il n'est pas du genre à lâcher facilement. Une chose est claire, il faudra compter sur Benjamin Dutreux lors du Vendée Globe 2024.  Diffusé le 22 septembre 2023 Générique : In Closing – Days Past Post-production : Grégoire Levillain

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