Podcasts about coinciding

On June 14, thousands gathered in Fresno and cities nationwide for “No Kings Day,” a protest movement opposing what demonstrators call authoritarianism under President Donald Trump’s second term. Coinciding with Trump’s 79th birthday and a military parade in Washington, D.C., the protests drew over 2,000 people in Fresno alone, rallying at key intersections like Blackstone and Nees. Protesters voiced concerns over immigration raids, budget cuts, and threats to democratic norms. Please Like, Comment and Follow 'Broeske & Musson' on all platforms: --- The ‘Broeske & Musson Podcast’ is available on the KMJNOW app, Apple Podcasts, Spotify or wherever else you listen to podcasts. --- ‘Broeske & Musson' Weekdays 9-11 AM Pacific on News/Talk 580 AM & 105.9 FM KMJ | Facebook | Podcast| X | - Everything KMJ KMJNOW App | Podcasts | Facebook | X | Instagram See omnystudio.com/listener for privacy information.

Federal authorities are stepping up their presence ahead of mass demonstrations planned for Saturday, June 14. ICE (Immigration and Customs Enforcement) is deploying Special Response Teams (SRTs) — elite tactical units — to five U.S. cities: Northern Virginia, New York, Philadelphia, Chicago, and Seattle.These deployments come just as hundreds of “No Kings Day” protests are set to take place nationwide, challenging the Trump administration's immigration policies and broader concerns about authoritarianism. The largest demonstration is expected in Philadelphia.Coinciding with the Army's 250th Anniversary Parade in Washington, D.C. — and President Trump's birthday — this weekend is shaping up to be politically and emotionally charged.

Coinciding with Julie's first public appearance, daughter Savannah announced on Instagram that both parents had reunited for the first time after serving sentences for bank fraud and tax evasion since January 2023.Advertising Inquiries: https://redcircle.com/brandsPrivacy & Opt-Out: https://redcircle.com/privacy

This episode of SpaceTime explores the recent surge in solar activity, including the largest solar flare of the year and the most intense geomagnetic storm in two decades.Massive Solar Flare and Its ImplicationsWe delve into the details of a powerful X 2.7 class solar flare that erupted from a newly active sunspot region, AR14087. Although the flare was not initially directed towards Earth, its rotation has now positioned it directly in our path. We discuss the mechanics of solar flares, their classification, and the potential impacts of such events on our planet, including disruptions to communication systems, satellite operations, and even power grids.The Gannon Storm: A Historic Geomagnetic EventThe episode highlights the Gannon Storm, a severe geomagnetic storm that struck Earth on May 10, 2024. Coinciding with a space weather exercise, this event caused significant disruptions, including high voltage power line failures and rerouted flights due to radiation exposure. We analyze its effects on the atmosphere, satellites, and even the ionosphere, revealing insights into how such storms can impact modern technology.Ancient Solar Storms and Their Modern ImplicationsIn a fascinating segment, we discuss a groundbreaking study that identifies the strongest solar storm ever recorded, dating back to 12350 BCE. This ancient event, significantly more intense than any modern storm, provides invaluable data for understanding solar activity and its potential risks to contemporary infrastructure.Science Robert: Long Work Hours and Brain ChangesWe also touch on a new study revealing how long working hours could alter brain structures, potentially affecting memory and emotional regulation.Join us as we unpack these cosmic phenomena and their implications for life on Earth and beyond.www.spacetimewithstuartgary.com✍️ Episode ReferencesJournal of Occupational Environmental Medicinehttps://journals.lww.com/joem/Pages/default.aspxBecome a supporter of this podcast: https://www.spreaker.com/podcast/spacetime-space-astronomy--2458531/support.00:00 Solar flares are powerful blasts of energy erupting from sunspots10:30 May 2024 was the biggest geomagnetic storm in over 20 years14:29 New study reveals strongest solar event ever recorded, rewriting science on space weather18:23 A new study claims people who work long hours could have altered brain structures

In this episode of Friday Field Notes, Ryan Michler explores how creating options leads to true freedom. Expanding on the concept of "discipline equals freedom," Ryan argues that personal responsibility, open-mindedness, and sovereignty are key to unlocking a life of choice. He shares four actionable strategies to cultivate options, emphasizing self-improvement, avoiding rigid thinking, aligning relationships, and prioritizing liberty. Ryan inspires listeners to take control of their lives and pursue their desired path. Join the Iron Council at orderofman.com/ironcouncil for more. SHOW HIGHLIGHTS 00:00 - Introduction to Options and Freedom 02:35 - Fix Yourself First 04:59 - Never Pedestalize Anything 09:43 - Coinciding vs. Conflicting Interests 14:05 - Sovereignty as the Path to Liberty 17:45 - Reclaiming Your Sovereignty 20:00 - Closing Thoughts and Call to Action Order Ryan's new book, The Masculinity Manifesto. For more information on the Iron Council brotherhood. Want maximum health, wealth, relationships, and abundance in your life? Sign up for our free course, 30 Days to Battle Ready

Coinciding with National Bike Week, 10-18 May, Payzone, Ireland's largest consumer payments network, is excited to announce an expanded partnership with Bleeper, Dublin's longest-running stationless bike service. Building on a successful partnership since 2023, Payzone has renewed its sponsorship of Bleeper's fleet of over 800 public bikes, operating across Dublin City, Fingal, and Dún Laoghaire-Rathdown County Councils, for a further two years. In addition to the renewed sponsorship, Payzone has now added new functionality and features for active travel to its popular Payzone app, empowering users to not only locate the nearest Bleeper bike but also unlock and pay for it seamlessly using their Payzone account. At the core of this partnership is a commitment to sustainability. Bleeper's mission is to fight climate change, "one journey at a time". In 2024 alone, Bleeper users avoided emitting approximately 46,520kg of CO2 by choosing to cycle for their daily trips. By integrating these services into the Payzone app, users now have even greater access to environmentally friendly travel options. Jim Deignan, CEO of Payzone, commented: "This integration with Bleeper reflects our commitment to making everyday easier; in particular to make travel and mobility easier and more accessible to those commuting in the city. In addition to simplifying everyday transactions, we are also actively promoting a greener future for Irish towns and cities." Payzone is committed to continuous innovation, enhancing its users' experience by integrating more value-add services. Payzone was the first app in Ireland to integrate shared bikes into its platform offering with the company planning to add further modes of transport in the future. Hugh Cooney, Founder of Bleeper, added: "This partnership with Payzone represents a step towards making bike-sharing even more accessible to the public. The integration offers an easy and affordable way for more people to choose cycling as a sustainable transport option. We are thrilled to work with Payzone and look forward to further expanding these services." For more than a decade, Payzone's mobile application has been a trusted platform for motorists, delivering continuous innovation. Payzone's application offers a unique blend of parking, transport & micromobility solutions. Operating across18 counties, the Payzone app makes it easy to find and pay for parking, manage toll payments, access shared mobility options and save with exclusive offers, all in one app. See more stories here.

Coinciding with the papal conclave of 2025 as cardinals reverently decide who will be the new Pope, we dive into a pervading mystery that the Vatican once had (and possibly still has) its hands on a working time machine...A story which takes in Nobel Prize winners and Nazi scientists, let's find out the answer to the question 'does the Pope have a time machine?'______An exclusive extended, ad-free version of this episode with over 20 minutes of bonus extra chat can be found over at our Patreon!Extended episodes drop over there usually 3 days early and with zero ads so if you enjoy Mystery on the Rocks then please consider heading over there to support us, where there is already a huge backlog of exclusive extras such as extended episodes, bonus episodes, minisodes, outtakes, cocktail recipes and more!Hosted by Masud Milas, Chris Stokes, and Sooz Kempner Mystery on the Rocks is a high concept comedy and true crime/unexplained phenomena podcast set in a fictional mystery-solving bar with real cocktails!. The focus of the show is to attempt to crack a real, unsolved mystery from history – true crime and bizarre occurrences, all with a whodunnit or WTF happened question hanging over them.You can follow us on Bluesky, X and Instagram too! Hosted on Acast. See acast.com/privacy for more information.

TALK TO ME, TEXT ITEaster Monday brings a mix of solemn reflection and heated debate as we discuss Pope Francis's unexpected passing and what this means for Catholics worldwide – both devout and those who've stepped away from regular religious practice.The conversation takes a sharp political turn when examining former President Trump's recent "thinking out loud" comment about deporting "homegrowns next." This off-the-cuff remark ignited immediate controversy with political commentator Simone Sanders and Representative Glenn Ivey promoting the unfounded fear that Black Americans could be targeted for deportation. We cut through the race-baiting rhetoric to analyze what Trump likely meant about violent criminals while acknowledging the constitutional impossibility of deporting American citizens.Perhaps most passionate is our examination of the Boston Marathon's gender division policies. Coinciding with Patriots Day's 250th anniversary, this iconic American sporting event has permitted biological males to compete in women's divisions since 2018. We highlight the case of Ria Susing (born Robert Sheen Young), who has competed in female categories over 338 times, winning medals in 140+ instances – each victory displacing deserving women athletes. This practice fundamentally undermines athletic fairness and the competitive opportunities women fought decades to secure. When even "Women's Running Magazine" features biological males on covers meant to champion female athletes, we must ask: what spaces remain protected for women in sport?The episode concludes with a thought-provoking question about political awakening. What issues first captured your attention in your formative years? Was it military service, civil rights, environmental concerns, or something entirely different? Share your story and join the conversation about how these early influences shape our lifelong civic participation and values.Buzzsprout - Let's get your podcast launched!Start for FREE Thanks for listening! Liberty Line each week on Sunday, look for topics on my X file @americanistblog and submit your 1-3 audio opinions to anamericanistblog@gmail.com and you'll be featured on the podcast. Buzzsprout - Let's get your podcast launched!Start for FREESupport the showTip Jar for coffee $ - Thanks Music by Alehandro Vodnik from Pixabay Blog - AnAmericanist.comX - @americanistblog

 Today on Too Opinionated, we sit down with singer Keith Mitchell to talk about “He's Alive,” his rousing, praise-filled gospel fired soul debut single as a solo artist. Keith is finding his own voice as a solo artist and fully embracing his musical destiny after years of success recording and touring as part of the 80's-90's legendary, Grammy-Nominated R&B vocal group After 7. Founded in 1987 by Melvin and Kevon Edmonds, and long-time friend Keith Mitchell, the trio was initially produced by mega hit-makers Babyface (the Edmonds' younger brother) L.A. Reid, and Daryl Simmons in the group's self-titled 1989 debut album which spawned the Billboard #1 R&B (and Hot 100 Top Ten) hits “Ready or Not” and “Can't Stop.” They released two more albums (including the platinum-selling Takin' My Time) over the next decade before their initial split. Reforming in the late 2000s, After 7 resumed touring with Melvin's son Jason replacing him. Melvin rejoined them for their 2015 comeback single with the Top 10 AC hit “I Want You,” and their fourth album Timeless. With a few more personnel changes in the wake of Melvin's 2019 passing, After 7 released its fifth album Unfinished Business in 2021. Coinciding with the drop of “He's Alive,” Mitchell officially left the group in January.  A powerful showcase for Keith's ultra-infectious vocal, rap and songwriting talents, “He's Alive” – the lead single from his upcoming debut album Food for Your Life - is an overflowing expression of the singer's great joy over the living presence of God in his life.    Want to watch: YouTube Meisterkhan Pod (Please Subscribe)

Our Grand Tour reaches one of its strangest destinations this week as we complete our trilogy of Tezuka Osamu-themed episodes with a look at the Animerama Trilogy, a collection of three experimental animated films for adults created by Mushi Productions between 1969 and 1973. Coinciding with the Japanese New Wave movement and the rise of ‘Pink Films,' these movies are stylistically anarchic, occasionally graphic, and range from irreverent and immature to startlingly sophisticated. Consisting of 1969's A Thousand & One Nights, 1970's Cleopatra, and 1973's Belladonna of Sadness, all directed by Yamamoto Eiichi, these films were part of a global wave of efforts to make elaborate feature animation aimed squarely at adults, and while none were successful enough to pull Mushi Pro out of bankruptcy, they have endured as a fascinating experiment from a time when anime was still finding itself – and the last film, Belladonna of Sadness, is absolutely a masterpiece within its own right. Enjoy, and come back next week as we put on our tin-foil hats, get paranoid, and watch the classic 2006 anime Welcome to the N.H.K.! Time Chart:Theme Song: 0:00:00 – 0:01:15Intro and History: 0:01:15 – 0:31:21A Thousand & One Nights Review: 0:31:21 – 1:26:29Eyecatch Break 1: 1:26:29 – 1:27:14Cleopatra Review: 1:27:14 – 2:09:43Eyecatch Break 2: 2:09:43 – 2:09:59Belladonna of Sadness Review: 2:09:59 – 3:25:21End Theme: 3:25:21 – 3:26:22Subscribe to our YouTube channels! Japanimation Station: https://www.youtube.com/c/japanimationstation  Purely Academic: https://www.youtube.com/@purelyacademicpodcastRead Jonathan Lack's movie reviews and stay up to date with all our podcast projects at https://www.jonathanlack.comSubscribe to PURELY ACADEMIC, our monthly variety podcast about movies, video games, TV, and more: https://purelyacademic.simplecast.comRead Jonathan's book 200 Reviews in Paperback or on Kindle – https://a.co/d/bLx53vK“Welcome to Japanimation Station” – Music by Thomas Lack, Lyrics by Sean Chapman, featuring Hatsune Miku. “Rolled Into One” – Music & Lyrics by Thomas Lack, featuring Hatsune Miku. https://www.thomaslack.com

Coinciding with International Women's Day this week, this special episode of AI and the Future of Work highlights key conversations with women leading the way in AI ethics, governance, and accountability.In this curated compilation, we feature four remarkable experts working to create a more equitable, trustworthy, and responsible AI future:

Send us a textWe're baaaack! In season three we're covering all things spatial data science. Coinciding with the launch of the Center for Spatial Studies and Data Science at UC, Santa Barbara, this season Trisalyn's talking with researchers in the field to learn how spatial data science can help us solve big problems facing our planet.

Coinciding with the official opening of the East Meath Civic Centre in Bettystown. Late Lunch came live from what Gerry described as the most beautifully appointed studio from which he had ever broadcast his show! We heard from the Chairperson of Meath County Council Sharon Tolan, CEO Kieran Kehoe, Executive Librarian Aoife Carberry, Architect Robin Lee and Environmental Awareness Officer Bernadine Carry. Hosted on Acast. See acast.com/privacy for more information.

This episode of Man2Man360, hosted by Darryl Anderson, delves into the importance of aligning with like-minded individuals who share a Biblical worldview rather than simply rallying based on shared ethnicity. Coinciding with Black History Month, the discussion features a critical look at a social media clip about Carter G. Woodson's views on rugged individualism and the pros and cons of socialism within the Black community. The episode emphasizes the necessity of trusting in God for guidance and success over reliance on governmental systems and the importance of fellowship with believers.00:00 Introduction and Purpose of the Show01:39 Black History Month and the Debate04:31 The Audio Clip and Its Implications07:02 Discussion on Black Wall Street and Self-Reliance16:52 Trusting God vs. Trusting Systems31:55 Final Thoughts and Wrap-UpVISIT OUR WEBSITE for Man2Man 360Show is Recorded, Edited and Produced by Darryl D Anderson of Ambassador Media GroupPLEASE SUBSCRIBE to our YouTube page as we need your help getting the word out! YouTube Page: youtube.com/@man2man360Podcasts drop every Saturday at 9am. Live Airing of the show is on http://rSpirit.Online - Thursdays 8pm, Saturdays 8am and Tuesday NOON Get the rSpirit.Online appLive Airing of the show is on Opposition Radio at  https://TheOppsRadio.Live - Saturdays 8am Please visit, LIKE and Comment about the show at our Facebook.com/Man2Man360 Also visit our radio station page at Facebook/rSpirit.Online;  Intro Theme Song Edited by Darryl Anderson (AMG) and Mixed by Damion Hill of https://e-mixonline.com   VoiceOvers by Christopher Bell & Daphne BryantLicensed to use song:Tough Kid https://www.premiumbeat.com/royalty-free-tracks/tough-kidIt's Raining Againhttps://www.premiumbeat.com/royalty-free-tracks/it-s-raining-againBlue Note Bouncehttps://www.premiumbeat.com/royalty-free-tracks/blue-note-bounceSFX - https://musicradiocreative.com/VIDEO CLIP: https://www.instagram.com/reel/DGJCx6ouwQl/?igsh=Y2swNzRyczIwdzlkCarter G Woodson: https://www.historyisaweapon.com/defcon1/misedne.htmlTry our NEW Fan Mail experience and send us a Text Message from HERE!

Fans of record-breaking blockbuster Chinese movie Ne Zha 2 are making significant waves in the derivatives market, clearing out retailer inventories and even creating DIY character-shaped dolls and food items. 中国破纪录票房大片《哪吒2》的粉丝们在衍生品市场掀起巨大波澜，清空了零售商的库存，甚至自制角色玩偶和食品。 Since the film's debut on the first day of the Chinese New Year, which was Jan 29 this year, sales of its collectibles, ranging from mystery toy boxes and cards to fridge magnets and badges, have reportedly topped 50 million yuan ($6.97 million) on Taobao, a leading e-commerce platform in China. 自今年1月29日（农历新年第一天）上映以来，据报道，其衍生品在淘宝（中国领先的电商平台）上的销售额已突破5000万元人民币（约合697万美元），包括盲盒玩具、卡片、冰箱贴和徽章等。 This sequel to the 2019 hit Ne Zha, with inspirations derived from Chinese mythological tales, has already drawn over 200 million cinema-goers, the highest number in the country's film history. 作为2019年爆款电影《哪吒》的续集，这部取材于中国神话故事的影片已吸引超过2亿观影人次，创下中国电影史上的最高纪录。 The film became an instant holiday box office hit thanks to its contemporary re-imagination of Ne Zha, a well-known mythical figure with extraordinary powers, and via its intriguing plot twists. 这部电影通过对哪吒这一拥有非凡力量的著名神话人物的现代重塑以及引人入胜的剧情转折，迅速成为春节档票房爆款。 Customers inquiring about toys featuring characters from the film are often left disappointed at stores across China. A salesperson at a trendy toy store in downtown Nanjing in East China's Jiangsu province said even display samples were sold out. "We expect to restock items like laser cards later." 在中国各地的商店，询问电影角色玩具的顾客常常失望而归。江苏省南京市市中心一家潮流玩具店的销售人员表示，甚至连展示样品都已售罄。“我们预计稍后会补货激光卡片等商品。” Notably, Hunan Sunny & Sandy Toys Manufacturer Co Ltd, the film's sole licensed manufacturer of 3D food-grade plastic toys in China, reported sales of over 450,000 mystery toy box sets through live-streaming in just 11 days -- ranking first in terms of the sales of board-game merchandise on the video platform. In addition, more than 10 million of these sets have been sold through offline partnerships. 值得注意的是，湖南阳光与沙地玩具制造有限公司（该片在中国唯一授权的3D食品级塑料玩具制造商）报告称，仅11天通过直播销售了超过45万套盲盒玩具，在视频平台的桌游类商品销售中排名第一。此外，通过线下合作伙伴销售了超过1000万套。 Yang Zhenlin, assistant to the company's chairman, said their factory workshops had to resume operations ahead of schedule after the Spring Festival holiday, with their hundreds of staff members working tirelessly to replenish inventory. "We had great confidence in the film even before its release, so we promptly secured the copyright," Yang told Xinhua. 该公司董事长助理杨振林表示，春节假期后，工厂车间不得不提前复工，数百名员工加班加点补充库存。“我们在电影上映前就对其充满信心，因此迅速获得了版权。”杨振林对新华社表示。 This week, on e-commerce platforms, some stores have gradually restored supplies. Businesses in the second-hand market have remained brisk. 本周，在电商平台上，部分商店已逐步恢复供应。二手市场的交易依然活跃。 Fans have also discovered that the gold bracelets they had purchased after the first Ne Zha film came out in 2019, with designs inspired by the "universe ring" on Ne zha's arm, have tripled in value on the second-hand market, thanks to both the success of Ne Zha 2 and a higher gold price. 粉丝们还发现，他们在2019年第一部《哪吒》电影上映后购买的金手镯，其设计灵感来自哪吒手臂上的“乾坤圈”，由于《哪吒2》的成功和金价上涨，在二手市场上的价值已翻了三倍。 Some fans have gone so far as to make their own versions of it, using wood, plasticine, flour and even thread. Coinciding with the Lantern Festival on Feb 12, netizens shared creative improvisations of Ne Zha-shaped glutinous rice dumplings, a festive food. 一些粉丝甚至用木头、橡皮泥、面粉甚至线自制了哪吒角色。2月12日元宵节当天，网友们分享了以哪吒为灵感的创意汤圆，这是一种节日食品。 Miao Lingyi, a 10-year-old girl living in East China's Shanghai, expressed her admiration for the character Ao Bing, the son of the Dragon King, stating her desire to use her pocket money to buy a collectible featuring him. "I really love the character and I don't mind waiting a while for the collectible," she said. 居住在上海市的10岁女孩缪灵怡（音译）表达了对龙王之子敖丙这一角色的喜爱，并表示希望用零花钱购买相关收藏品。“我真的很喜欢这个角色，我不介意等一段时间再买到收藏品。”她说。 According to experts, the film's huge success stemming from its captivating plot and stunning special effects, has evoked emotional attachment and resonance with characters among its audiences, while some related products feature limited edition designs -- thereby enhancing their value as collectibles and stimulating consumer purchasing enthusiasm. 专家表示，这部电影的巨大成功源于其引人入胜的剧情和震撼的特效，激发了观众对角色的情感共鸣，而一些相关产品采用限量版设计，从而提升了其收藏价值，刺激了消费者的购买热情。 Ye Guofu, founder of MINISO, a Chinese retailer known for its fashionable but affordable household products, said that Chinese consumers' growing focus on emotional value attached to commodities, particularly among the younger generations, is expected to further drive the consumption of IP-featured products, such as those related to domestic animated films and games. 名创优品（以时尚且价格实惠的家居产品闻名的中国零售商）创始人叶国富表示，中国消费者对商品情感价值的日益关注，尤其是在年轻一代中，预计将进一步推动IP衍生品的消费，例如与国产动画电影和游戏相关的产品。 With this lucrative market rapidly expanding, experts have stressed the importance of both IP innovation and product quality, while warning against risks of market irregularities and intellectual property rights violations. 随着这一利润丰厚的市场迅速扩张，专家强调了IP创新和产品质量的重要性，同时警告市场乱象和知识产权侵权的风险。 Law professor Zheng Ning with Communication University of China suggested that market regulators strengthen oversight to combat potential price gouging and the sale of substandard products -- thereby ensuring a more orderly market environment. 中国传媒大学法学教授郑宁建议，市场监管部门应加强监管，打击哄抬价格和销售劣质产品的行为，从而确保更有序的市场环境。 Zhao Liangshan, a lawyer in Northwest China's Shaanxi province, cautioned that handcrafted items made for personal use are not allowed for commercial purposes. 陕西省律师赵良山（音译）提醒，个人手工制作的物品不得用于商业用途。 As Ne Zha 2 enters international markets, Hunan Sunny & Sandy Toys Manufacturer Co Ltd aims to target global markets -- particularly in Asia, North America and Europe. 随着《哪吒2》进入国际市场，湖南阳光与沙地玩具制造有限公司计划瞄准全球市场，特别是亚洲、北美和欧洲。 The film is set to be screened in various countries, including the United States, Canada, Australia, New Zealand, South Africa, Egypt, Singapore, Japan and the Republic of Korea, with premieres in Los Angeles and Sydney having received positive responses from professionals and fans alike. 该片将在多个国家上映，包括美国、加拿大、澳大利亚、新西兰、南非、埃及、新加坡、日本和韩国，洛杉矶和悉尼的首映式已获得专业人士和粉丝的积极反响。

Shannon Airport says Ireland must re-examine its aviation policy which it claims "bizarrely penalises" smaller airports experiencing growth in passenger numbers. The Clare base and a major Irish airline have issued a joint call for the passenger cap of the Government's Regional Airports Programme to be increased so as to ensure Shannon can continue to avail of State funding. The call comes as Ryanair has unveiled its summer 2025 schedule for Shannon Airport which features 26 routes including a new route to Madeira. Increased frequencies have been confirmed for eight other routes, specifically Alicante, Edinburgh, Faro, Kaunas, Krakow, Malaga, Porto, and Reus. The airline has also announced that extra seats have been added to and from La Rochelle in April ahead of Munster's highly anticipated European Rugby Champions Cup match with the French side. Having operated out of Shannon for 38 years, the announcement sees Ryanair's traffic growth at the Clare facility grow by 17%. The airline's Chief Marketing Officer Dara Brady says if more routes are to come to Shannon, the region must demonstrate that tourists want to come here. Coinciding with the schedule's release, a joint call has been issued by Shannon Airport and Ryanair for a seismic shift in Irish aviation policy. Over the past number of years, Shannon has benefited from the Government's Regional Airports Programme which supports facilities carrying up to one million passengers. As Shannon saw 2.1 million passengers pass through its gates last year, it now falls outside the eligibility criteria for the programme. Both the Clare base and Ryanair are now calling for this cap to be lifted to three million, and the inclusion of a commitment to conducting a review of National Aviation Policy in the Programme for Government has offered hope that this could become a reality. Shannon Airport Group CEO Mary Considine says the facility mustn't become a victim of its own success.

Send us your thoughts! Swedish jazz virtuoso Ebba Åsman has announced the forthcoming release of her third full-length record When You Know. The new album arrives March 21st, 2025 via Dorado Records.Coinciding with the announcement of ‘When You Know' of the upcoming album are the joint first singles - the title track ‘When You Know' and ‘No Answer'. The pair of songs channel the feelings that came into clarity for Åsman during her time in the woods: the stresses of not knowing where you're headed, sensing that you're losing grip of the life you've built, drowning in the infinite questions that swirl around in your head – and ultimately, accepting the uncertainty of it all. The latter track has been described as the turning point of the album, where acceptance of the circumstances begin to prevail.Coming off of a Swedish Grammy (GRAMMIS) nomination for her 2023 sophomore album ‘Be Free', live showings at North Sea Jazz Festival and London's Ronnie Scott's and an appointment as one of Yamaha's brand ambassadors, the trombonist, songwriter and producer sought to quiet the noise around her and challenge the jazz genre's rigid rules for her next project. The end result is ‘When You Know'; a smoky and melancholic 10-track cocktail of jazz, alternative R&B, indie, Hip-Hop and ambient sonics that experiments at every turn. On hand to co-produce the record and provide the electronic elements that move ‘When You Know' away from the jazz world and into more avant-garde territory, Ebba collaborated with Berlin-based producer Lucy Liebe. Packing a potent emotional punch into a running time of just 31 minutes, the 10 tracks are a reflection of Ebba herself: direct, driven, precise. Retreating to a cabin outside of her small hometown of Hammarö, 200 miles west of Stockholm, she recorded the album in the dead of winter. With the temperatures outside nearing minus-thirty degrees, Åsman logged off for a month – disconnecting from TV, social media and emails. Embracing with vigour both the deep sense of calm and the challenges that come with the cold but also the stillness and solitude that is yielded being in the wilderness.Though this is Åsman's third studio album, it will be the first time she's singing on record. An important statement and moment of transition for Ebba. Elaborating on this further she said: “If you're singing, you are the closest you can be to your own expression but I wanted to first be respected as an instrumentalist. If you're a woman and you tell people you're a musician, everyone assumes and says “Oh – so you're a singer?”. ‘When You Know' will mark the moment on which Ebba Åsman's exceptional gifts are finally crystallised. At age 7, she began learning trombone and by 15, she won a place to study the instrument at the Södra Latin School in Stockholm. The renowned hot-house for Swedish talent whose alumni include Lykke Li, Yung Lean and the prolific hit songwriter Max Martin. But when she moved to the Netherlands to study at the Rotterdam Conservatory of Music, she began to push against the constraints of formal learning.  Self-identifying as a “jazz rebel”, rather than being preoccupied with the theoretical and mechanical aspects of jazz, Ebba operates from a mode of pure intuition and feeling. At just 26, ‘When You Know' finds Åsman continuing to push the boundaries of jazz through the two distinct sides of her musical self: the notes she conjures from the trombone and now, her voice.Support the show

In this episode, The Daily reports on how students and different leaders of political student organizations are reacting to the inauguration landing on Martin Luther King Jr. Day. Read the full story here: https://dailynorthwestern.com/2025/01/21/audio/296124/

The Genetic Rare Syndromes Observational Cohort (GenROC) study aims to improve our understanding of how rare genetic conditions affect the way children grow, their physical health and their development. Through actively involving parents as experts in their child's condition, the study seeks to gather valuable insights and ensure that family experiences shape future research and care strategies. You can find out more about the study and eligibility criteria via the Bristol University website. In this episode, Jillian Hastings Ward, patient advocate and former Chair of the Participant Panel at Genomics England, is joined by Dr Karen Low, a clinical geneticist leading the study at the University of Bristol, who shares insights into its objectives, the importance of a co-production approach with families, and the vital data being collected in the study to improve support for these children and their families. We'll also hear from Lindsay Randall, a parent who discusses the journey of receiving a rare diagnosis for her child, highlighting the critical need for more comprehensive information and community support. "If you join GenROC, that data will be used to develop a growth chart for your child essentially and their genetic condition, so I'm really excited about it because I feel like that's a very concrete definite given now for all the families in GenROC, which is just brilliant." You can download the transcript or read it below. Jillian: Welcome to Behind the Genes Lindsay: Historically, there's been a significant absence of patient voice in rare disease research and development, and knowing that's changing, I think that's really empowering for families and to know that professionals and industry are actually listening to our stories and unmet needs and really trying to understand, and that offers much greater impact on the care and treatments of patients in the future. Jillian: My name is Jillian Hastings-Ward. On today's episode I'm joined by Dr Karen Low, Consultant Clinical Geneticist and Chief Investigator for the General Cohort Study, and Lindsay Randall, Paediatric Practice Development Nurse and founder of Arthur's Quest, which is a UK registered, non-profit, raising awareness for the ultra-rare condition: SLC6A1, developmental and epileptic encephalopathy. Welcome to you both. Today we'll be discussing the GenROC study, which is aiming to understand more about the health, development and valuing the experiences of children with neurodevelopmental conditions. If you enjoy today's episode we'd love your support. Please like, share, and rate us on wherever you listen to your podcasts. Thank you both very much for joining us today, Karen and Lindsay. There's a lot we want to cover, but first of all it would be great just to put a little bit of context around the Gen-Roc study. Karen, can you tell us a bit about what the study is aiming to do, who is eligible and why do you want them? Karen:  Thank you. And thank you so much for having me today, Jillian. So, the GenROC study, first to just explain to people what ‘GenROC' stands for. GenROC stands for the Genetic Rare Syndromes Observational Cohort Study. Just to give you some context about the study, I'm a clinical geneticist and most of my clinical work focuses on paediatrics, so I see children in my clinics and the sort of children I see generally are children with rare genetic syndromes. The last five to ten years we've got much better at diagnosing children with these rare conditions and that's because testing has got so much better. We can now do whole genome sequencing and we can do that on the NHS, which is amazing, children can get their tests as part of their clinical care, so it means that a lot more children are being diagnosed with rare conditions, about 2,000 per year in the UK. And the thing about that is, that I see these children in my clinics and I give their families that diagnosis. But the problem is for so many of these ultra-rare conditions, like Lindsay's family has, we sit there and we say to the family, “Well, your child has got ‘X' condition,” and we give them some information from maybe one or two publications and linked to a leaflet and a Facebook group. And then we say, “But really we don't know that much about this condition.” And they say, “But what is it going to mean for them when they are growing up or when they are adults? Will they be able to finish school? Will they be able to work? What is it going to mean?” And I have to shrug my shoulders and go, “I'm not really sure.” And as a geneticist and as a doctor and as a mother really, I just felt that wasn't good enough, and I found it really frustrating and I know that the families that I work with, that I look after, also find it frustrating and I wanted to do better. And I also found it frustrating that for many genes, researchers would publish two or maybe three publications about these conditions, and then they would move on to the next novel gene, and actually, the journals are a bit like that as well, they like novel things, they like new conditions, they like the next gene. And so, it means that actually data doesn't always carry on being gathered in these rare conditions, and there are a lot of them. That was another thing, I sort of felt that these conditions were being done a disservice and that we needed to do better, so that's where the whole idea of the GenROC study came from was my drive and desire to improve things for families and actually to work with families to improve that, and that's where so this is a very highly co-produced study and right from the outset I've involved parents in telling me what they wanted to know and I've got a very, very active PPI group, full of parents of children who have got rare genetic conditions, and also I'm really lucky to have a young adult who has a genetic neurodevelopmental disorder herself and they all tell me about essentially what I should do and what I shouldn't do. They tell me when I'm not doing enough or when I need to do something differently, so it's very highly co-produced, they're highly involved all along the way. So, children with a confirmed genetic diagnosis in a list of eligible genes which people can see on our website if they Google GenROC University of Bristol, we've got a very easy checker for eligible genes, but they are essentially the most frequently diagnosed genes in rare neurodevelopmental disorders. And if their child is under 16, has a confirmed diagnosis and doesn't have any other genetic diagnoses then they can go into the GenROC study, that's essentially the eligibility criteria. Jillian: That's really interesting. It's very helpful to hear the background and I think as a parent of a child with a very rare disorder hearing that the clinicians also recognise this gap and the sort of pause that happens once you have your initial diagnosis, is really helpful and really encouraging. Lindsay, can we turn to you next and can you unpack a little bit about what it meant for you to get a rare diagnosis for your child and what point on your family journey was that compared to where you are now? Lindsay: I think to get a rare diagnosis for us was difficult and challenging and I think the first kind of challenge that any family has is actually being well-informed by a paediatrician who is also well-informed, and that's not always the case. That can affect the way we acknowledge or accept a diagnosis and how we also access support and how we understand what more we can do to make more connections. We did have genetic counselling offered, but I think there are families out there who don't get genetic counselling offered to help them understand the child's diagnosis, and then there's a heavy reliance on the internet, and as you said, there's a lack of information out of there. A lot of conditions are newly diagnosed or they're very complicated genes to work with, or as Karen said, they've had a couple of papers and people have moved on. And I think that does cause an immense feeling of isolation. We were diagnosed in 2018, our son, our first child, and exactly as Karen said, it was a fairly quick appointment of, “We don't really know much about this condition at the moment, there's a couple of papers. We know of 34 children in the world at the moment with your condition. Here's a Facebook group,” which we did join. And it is overwhelming to be given a diagnosis that's delivered with such little hope I guess, finding sources of information that's valid and robust is challenging, not everyone knows how to do that or has a skillset to conduct searches of academic research and I think that clinicians could definitely do better in also signposting the kind of umbrella charities like Unique and Contact and Swan and patient organisations, because I know that would have been definitely helpful for us as a family to be able to have opportunities to connect with others. Jillian: Thank you. Our diagnostic journey has been a bit a similar in that we were diagnosed through the NHS, and that at the time my son was the first person diagnosed with his disorder in the whole of the UK so it was really a big question mark, it was a question of our geneticist saying, “Here's the three PDF articles that we know exist in the world about this condition. Can you read them and tell us whether you think that sounds like him in order for us to be confirming our diagnosis?” I very much hear what you're saying there about feeling lost in the wilderness. And we too joined a Facebook group quite shortly after we got our diagnosis, and at the time my son was among the older ones or certainly as time has gone by he has been among the older children, so it can be really hard to know what might happen next. I think that now as Karen was saying we're getting much better at diagnosing people thanks to all the extra testing that's happening, that happens much earlier in life than it has done in the past, but I think then it still leaves a gap in parents' understanding because you don't necessarily know what the next ten years might look like for example. And so, I think making connections with people who are in that age bracket can be really important, but it's very hard to do. So Lindsay, I'm conscious that your professional training as a nurse must have stood you in quite good stead when you were faced with a barrage of medical literature shortly after your diagnosis, but I think one thing that every parent shares is the desire to do the best for their child and especially in this world of rare disorders. There's a huge amount of energy that comes through the community I think, faced with the need to try and self-start and build these networks and connections for themselves. Is that something that you've seen in your community as your experience? Lindsay: Yes, definitely. I think we're a growing community and over the years of course more and more children and young adults have been diagnosed with a few older adults coming through. It is very much a global networking effort and parent/patient organisations have been set up in many countries now by parents of children with children with SLC6A1. I definitely think that drive to become an expert in your child's condition is a long journey and one of continual learning and actually a lot of families simply don't have a capacity to take that on, I think often the medical and scientific jargon is difficult to understand and that makes it challenging to access. And as you said, as a paediatric nurse, I at least have some existing skills to understand healthcare to read the research and speak with medical and scientific professionals with some confidence, but in some ways, that has increased the burden I've placed on myself to become an expert for my children and other children and families who are not in the same position as me. It does require a lot of dedication and time, and that does have implications on families because it's time away from our children and from home, and from the remnants of our lives that we desperately try to cling onto, to not lose all sense of ourselves. It's not often spoken about but I do see the strain it places on the families, as well where there's a lot of separation and divorce sadly in the rare disease communities, and often that's as a result of one parent's drive to be the expert, which seems to cause one parent to fulfil more burden of care and that fosters some level of resentment or sense of loneliness towards the other one. Jillian: There are some scary statistics out there around familial breakdown in this context, and it is something which there are so many factors at play, but it definitely seems to be quite widely recognised and definitely a problem. In terms of the time that people have to spend on liaisons with the research community and the clinical community, that could bring us quite nicely back into a question for you, Karen, about what kind of information the GenROC study is looking to collect from families, can you tell us a bit more about that, please? Karen: Yes, absolutely. As I said before, I've been very conscious of the sort of lives that our families are living, and listening to Lindsay, her story is very reminiscent of so many others and yours, Jillian. So I know families have about a gazillion hospital appointments, their children are often also very, very ill intermittently or a lot of the time, then they've got school stuff to deal with or they've got EHC plans to try and fight for. It's more than a fulltime job in itself just being a parent of a child with a rare disease and it's hard work, so me asking them to do anything else is asking a lot. Luckily, I find, with the families I work with, who are universally wonderful I should add, that they are actually just really enthusiastic anyway about research for their child's condition, and that's because there isn't enough information out there, so it's relevant and important to them. But because they have no time at all, and any time they do give is their own personal time when they could be finally putting their feet up and watching something on TV, I have to make it as low effort as possible. The questionnaire is all online, using a user-friendly and interface as we've been able to develop. It's very user-friendly, it takes 10-15 minutes to complete; they can come and go from the questionnaire as well. We only ask for one time point at the beginning, which is all the sort of stuff that most parents will be able to tell you off the top of their head as well, so they don't have to go looking for loads of information, apart from a height and a weight. Then later down the line we're going to ask for a second questionnaire, it's in the process of being finalised and again that will be the same amount of time, very easy to do, online, at their convenience. It was co-produced with the PPI group, they've tested it for me, I've had really good feedback and I've asked parents who are in the study as well for feedback. Everyone tells me it's not too difficult or burdensome for them to do. The secondary questionnaire has been very much informed by conversations with the parents that I had as part of a nest of qualitative interview study in GenROC, and that has driven that secondary questionnaire quite differently to what I thought it might be when we first set up the GenROC study. At the beginning I thought it might just be: have things changed for your child? Can you give us a bit more clinical data? But actually I realised that probably I will still gather that information, but they probably won't have changed that much within the timespan in the study because it will only be a year or two after they completed the first questionnaire, and actually I realised that it would be much more useful to look at the impact of the genetic diagnosis, look at how they're accessing services within the NHS, what sorts of services they are accessing, Impact on the family and also looking at priorities for families. So families have talked to me about what their priorities are in rare disease, both in service provision but also in research, and I really am a very strong believer that we need to be given the limited funding, we need to be doing the research that matters the most to the families, not to the researchers. What do families actually want us to look into? Actually, do they want us to be looking into behaviour and what strategies work best for example, rather than something else very medical – what matters the most? And so that's going to be a specific question in that secondary questionnaire, really trying to identify what matters to families the most and then how that can be translated into clinical research in the future. So I'm really interested to see what's going to come out of that. Lindsay: I think that sounds brilliant, Karen because I think historically there's been a significant kind of absence of patient voice in rare disease research and development, and knowing that that's changing, I think that's really empowering for families and to know that professionals and industry are actually listening to our stories and unmet needs, and really trying to understand, and that offers a much greater impact on the care and treatments for patients in the future and certainly it makes endpoints more relevant to families as well. Jillian: What kind of outputs are you going to be looking at? Karen: The height and weight, the reason I'm asking for that is really because we are trying to work on growth charts for children and that's because growth charts for children with rare conditions don't exist by enlarge, there are a very, very tiny number of rare syndromes or conditions that have their own growth chart. The problem is that most children with these sort of rare conditions that we're talking about are either quite small or quite big, and the problem is that the paediatricians look at their growth and they go, “Oh well, you're much bigger or much smaller than other children your own age, what shall we do about that?” and particularly the little tiny ones it causes lots and lots of concern, so quite often these sort of growth parameters mean that the paediatricians do lots and lots of tests or put feeding tubes down, or add lots of calories, so it can be quite invasive and interventional actually that sort of growth parameter. But actually, sometimes that's because of the genetic condition and no matter how much feeding you do it's not going to change anything. The difficulty is we don't know that for certain, and actually we need good growth charts where paediatricians can make that call, and conversely sometimes a child actually does need investigating and the paediatrician puts it all down to their genetic condition, and that's why we need these growth charts. So GenROC is aiming to gather growth data from all these children and then we're going to work closely with Decipher, which is a website that was developed through the DDD study, which already holds lots of data from that study, so we're building on the power of that study and we're going to be generating growth charts for all of these genes. We've developed a new method for producing growth charts for rare conditions where you've got small numbers of patients – that was never possible before, so we've already proven now for four conditions we can, so the next stage is using all the GenROC data, putting it into Decipher and coding it in. So, if you join GenROC, that data will be used to develop a growth chart for your child essentially and their genetic condition, so I'm really excited about it because I feel like that's a very concrete definite given now for all the families in GenROC, which is just brilliant. Jillian: And is that something which will be shared with the families individually? Karen: Really great question. I hadn't planned on sharing the growth charts individually with the families, but that's something I can also go back to my PPI group and discuss with them about whether that's something people would want, and also I have a newsletter which goes out every three months to the families, so I can certainly ask that question actually directly. It's going to be widely available, the growth charts, we're going to make sure that they're accessible to paediatricians and clinicians etc. but in terms of output to the study, definitely the growth charts, we're also hoping to have other clinically useful outcomes depending on the different genes that come into the study. We essentially have a cohort of children with rare conditions, everyone puts everything down to a specific genetic condition but we know that there must be other factors at play that influence how children do. And this is a really unique thing we're trying to do with GenROC actually, looking at aside from that genetic variant, that alteration, what other factors are influencing how children are doing? Because some of those might be modifiable, you know, or some of them there could be things that could be put in place to help improve outcomes. So I'm quite excited about that as well, because that's quite new and novel and not really been thought about in this context before, so that will be an output. And the other output is something that I'm working on with Unique, which is the rare disease charity who has worked with us on GenROC from the start, and they are involved in our PPI as well and that is going to be looking at a template, calling it a report at the moment, it's in very early days, but something that parents will be able to hold, it's going to have lots of drop-down boxes that can be tailored and modified for individual patients and children, which will be a bit of a guide that they can give to clinicians, professionals, education, telling them about their condition but also telling them on an individualised basis about what needs to be looked for in the future. Because parents tell me they are fed up of having to tell everybody about their child's condition constantly, all the time, over and over again. So what the point of this output would be is to try and ease that burden a little bit. This is very early stages but we're going to involved parents all along the way. Jillian: And is that something which builds on the hospital passport idea that we've seen emerging around the world over the last few years where parents can start off telling their child's story on their own behalf? Karen: So, it's come from my own lived personal experience of being a mother of a child with autism and I haven't really spoken about that publicly before, so it's something I'm saying for the first time. I have a child who has autism and I have had to navigate things like a DLA application form. Jillian: That's Disability Living Allowance. Karen: Yes, exactly, which is a horrendous form, it's the most horrible form to complete, probably apart from an EHCP plan form but it's a horrible form to complete, it's quite upsetting as a parent and it's also got millions of boxes that you have to fill in. But one of the things that really, really helped me when I was completing that was a charity who had come up with lots of drop-downs that you could select from that might be applicable to your child to help you complete this form. And so it made me really think, “Well, could we do something similar for our children with genetic conditions but come up with lots of dropdown options that might apply to their child in all sorts of different areas?” And that was the inspiration, it was that, and doing the qualitative study that I've already done with parents of children in GenROC who were telling me about how fed up they were of having to constantly tell everybody about their child's condition over and over again. Jillian: Yes, that's probably very helpful to empower families to use standard terminology across the different families because my own son has epilepsy as part of his condition but actually trying to describe what his seizures look like I'm not sure I'm using the right words to fit the right boxes to fit them into the right categories with the neurologist. So that level of standardisation is something that we definitely need embedded into the system in order for more people to be able to use this data more effectively, so that sounds very helpful. Lindsay, coming back to you, what are you hoping to get out of this study, or what are you hoping this study will do on your behalf for the world? What motivated you to take part? Lindsay: I think I would like to see all of the aims of the study realised and for the study data to be used to inform the development of standards of care for a wide range of conditions, those included in the study. I think it would be great if that information, as Karen said, is available not only to the participants but also to children diagnosed with those conditions in the future and also it's an opportunity to consider themes that are identified across the disease groups as that can also help inform future research and look at investigations into the mechanisms of disease and where actually therapeutics could treat maybe more than one disease at a time and increase potential for basket trials and early access programmes – thank you to Dr Karen Low and her team for conducting the project because it included a comprehensive list of rare diseases, it really does give parents and patients an opportunity to have a voice and to contribute, which is empowering, and it gives them a little bit of autonomy as well over their direction that science and research goes to. Jillian: Fantastic, thank you. Karen, can you tell us a little bit about the timeframe for the study? I realise that we haven't really touched on that so far. Karen: Yes absolutely, I'm aiming to recruit 500 children as a total. We're open at 22 sites across the UK. Coinciding with this podcast actually we've opened a second door for recruitment, so the way we've recruited so far has been through clinical genetic sites, which is the way we've done these sorts of studies in the past, like the DDD study. The problem is that that relies on clinicians identifying eligible patients and clinicians are very, very busy in the NHS. I have worked closely with Unique who have been doing a lot of publicity and the genetic alliance have done publicity as well for the study, so that's been one way of identifying eligible participants. And also just parent power through social media has been amazing. The second way we're going to recruit, and this is going to happen very soon, is through Genomics England. So, we are going to trial a completely novel way of recruiting to research through Genomics England and that is for Genomics England to identify eligible participants for GenROC and this would have been through the 100,000 genome study and then they're going to send them invite letters, inviting them to take part. So that's the next phase of recruitment, I think if we have more than 500 then that will be great too, we'll be able to include those comers too, so that's not a problem. But we don't know whether this will work or not in terms of a way of recruiting to research, this is completely new for Genomics England and I'm a bit of a guinea pig if you like through the GenROC study, but I was quite willing to be that guinea pig because I thought it might increase access. So there will be some parents who have not been told about GenROC who have not heard about it, and who would love to take part, so I feel like this is the way of really widening that net as wide as possible. Jillian: I think that is a challenge isn't it, especially in rare disease – there's no point doing a public broadcast about an initiative because you're going to hit so few of the people that you're interested in, so actually how you access the community is the first challenge and I'm really pleased that Genomics England will be able to help you there because I think that is a very useful route through. I think it will probably be quite reassuring to quite a lot of families who were on the 100,000 Genomes Project who have got a diagnosis of one of the conditions that you're interested in, and are now perhaps subsequently in the fallow period after you have a diagnosis, wondering what happens next, so I can imagine it might be quite good news for some of them at least that they are now being invited to do something further. And the reason that you're building forward and you don't want people who are currently in the deciphering developmental disorders study is because you're already using their data through another source, is that correct? Karen: Exactly. So absolutely, I don't want anyone to feel that I don't want them, that's really not the case. I do want them but we have their data already from Decipher, so we're building on the DDD data already, so they're already contributing which is just the beauty of it, because that's what we should be doing in rare disease, we should be building on previous research because you know, you don't want to be trying to reinvent the wheel. Jillian: Agreed. So if someone is listening to this and has a child with a rare developmental disorder and they are interested in finding out more, what are the steps they need to take? Karen: If they Google Bristol University, GenROC, they'll come straight to the webpage and everything is on there. There's a link that they can sign up, the patient information leaflet's there, the eligible gene list is there, all the information they need, including our email address. Jillian: And is there an upper age limit for recruitment? Karen: Yes, children have to be under 16 and that's because once they get to 16 many of these conditions have associated learning difficulties, and it's just very much more complex to try and recruit young adults, young people, with learning difficulties and given it was a cohort study we felt it was going to be too difficult at the moment. Saying that, I have a huge interest actually in how these conditions present in adulthood, and I'm actually conducting a much smaller study at the moment in KBG syndrome, looking at adults, and so I hope that my future research career will allow me both to follow-up the children in GenROC, so that would be my vision but also to be able to take this forward for other adults with rare conditions, that's my aim and goal in the medium to long-term, so watch this space for that. Jillian: That sounds very exciting, thank you. Lindsay: I think I would like to say to Karen that I really like the sound of the idea of following patients up into young adulthood and adulthood, as you said, that is definitely a kind of an unknown area in lots of the rare diseases, especially in our condition, SLC6A1, it was mutation and the disease was only really discovered in 2015, so it is fairly new and we have very, very few young people and adults coming through and being diagnosed and connecting with the rest of the community. So, being able to understand the trajectory of conditions better and especially conditions where actually the presentation it's quite a spectrum, and so the long-term outcomes for people with SLC6A1 can look quite different, so it's good to collate more information about that I think. Karen: I think it's really important, so that's definitely where I'm looking to for the future with GenROC and more widely, I think it's just something I'm really interested in and has huge relevance for parents and families. Jillian: Well, I think we need to wrap up there but thank you both very much Dr Karen Low and Lindsay Randall for joining me today as we've been discussing the GenROC study, and how the study aims to improve understanding of how rare genetic syndromes affect the way children grow, their physical health, their development, but also how the patient and parent communities can work more closely with researchers to end up delivering something which is of a huge benefit to everybody. If you would like to hear more about this, please subscribe to ‘Behind the Genes' on your favourite podcast app. Thank you for listening. I've been your host, Jillian Hastings Ward. This podcast was edited by Bill Griffin at Ventoux Digital and produced by Naimah Callachand.

Content Warning: This episode includes discussions of mental health and violence that some listeners may find distressing. Join The Good, The Bad & The Rugby for a poignant and unforgettable episode featuring Ben Cohen and Phil Vickery as they sit down with Tins and Payno to share their deeply personal stories of triumph, struggle, and resilience. Coinciding with the release of the highly anticipated documentary Unbreakable: England 2003 on TNT and Discovery+, the team explores the untold aftermath of England's historic 2003 Rugby World Cup victory. Cohen reflects on a personal tragedy that profoundly shaped his career, while Vickery shares raw and candid revelations about life after rugby. Together, they discuss their 20-year reunion and the impact getting back together will have. Season 5 is sponsored by Continental Tyres

Coinciding with Art Basel Week 2024, Fredric Snitzer Gallery in Miami just opened “always vacationing among flamingos”, a solo exhibition ...

Shiur given by Rabbi Yisroel Gottlieb on Halacha Niddah. Shiur given in Yeshivas Ohr Reuven, Monsey NY.

Making his Selador Sessions debut, we introduce Clemens from Vienna, who is better known as The Wash. With his music gracing UV, Forensic, Mago Alley and many more, we thought it was high time he delivered a mix for us. Coinciding with the mix, his new track ‘Fair Warning' is coming soon on Selador (a track he made with Mango), and he has been added to the Selador ADE party line up This Saturday at Loods 12, alongside Dave Seaman, Anthony Pappa, Danny Howells, Redfreya, Cris-H and Jaap Ligthart. Last few tickets available here https://ra.co/events/1941868 Tracklist: 01. Francesco Pico - Rise Like A Flower (Jochem Hamerling Remix) [Magnitude Recordings] 02. Joel Lokk - Doppelgänger [Mango Alley] 03. D-Nox & DJ Zombi - There Is Hope (Mike Griego PsychoFunk Remix) [Sprout] 04. D'Wachman - We Will Never Forget That Never Happened (Patch Park Remix) [Manual Music] 05. Max Graham & Second Sine - Hypercube (The Wash & Rauschhaus Remix) [Mango Alley] 06. Rockka - Amnesia (Mike Isai Remix This show is syndicated & distributed exclusively by Syndicast. If you are a radio station interested in airing the show or would like to distribute your podcast / radio show please register here: https://syndicast.co.uk/distribution/registration

Making his Selador Sessions debut, we introduce Clemens from Vienna, who is better known as The Wash. With his music gracing UV, Forensic, Mago Alley and many more, we thought it was high time he delivered a mix for us. Coinciding with the mix, his new track ‘Fair Warning' is coming soon on Selador (a track he made with Mango), and he has been added to the Selador ADE party line up This Saturday at Loods 12, alongside Dave Seaman, Anthony Pappa, Danny Howells, Redfreya, Cris-H and Jaap Ligthart. Last few tickets available here https://ra.co/events/1941868 Tracklist: 01. Francesco Pico - Rise Like A Flower (Jochem Hamerling Remix) [Magnitude Recordings] 02. Joel Lokk - Doppelgänger [Mango Alley] 03. D-Nox & DJ Zombi - There Is Hope (Mike Griego PsychoFunk Remix) [Sprout] 04. D'Wachman - We Will Never Forget That Never Happened (Patch Park Remix) [Manual Music] 05. Max Graham & Second Sine - Hypercube (The Wash & Rauschhaus Remix) [Mango Alley] 06. Rockka - Amnesia (Mike Isai Remix This podcast is hosted by Syndicast.

This week on the Team Lally Real Estate Radio Show, we interview Dr. Kim Cook and Tamah-Lani Noh from U.S Vets. We learn about their inspiring journey into veteran advocacy and how the U.S. Vets is leading the charge to end veteran homelessness. They highlight the critical services U.S. Vets provides, from housing and employment support to mental health services. We also hear exciting updates on their Tiny Homes project, which is open to both veterans and others in need. They explain how to connect with the U.S. Vets to explore housing and support options, and how you can get involved in their mission to make a real difference.We also have our Experts We Trust. Duke Kimhan from HI Pacific Property Management covers the importance of managing pests and termites in rental properties, highlighting the need for renters' insurance and addressing loss of rent during fumigation. Jodie Tanga from Pacific Rim Mortgage shares insights on current mortgage trends, explaining how inflation and market conditions are affecting rates and why today's rates are still better than last year.Who are Dr. Kim Cook and Tamah-Lani Noh?Dr. Kim Cook is the Vice President of Clinical Services at U.S. VETS. Born and raised on O‘ahu, she has dedicated her career to supporting veterans, overseeing programs that provide housing and care for nearly 850 veterans each night. She is a passionate advocate for holistic wellness and community service. Tamah-Lani Noh is a retired veteran with 30 years of service in the Hawai'i Air National Guard and U.S. Air Force. She's currently the Program Director and is known for her leadership in drug prevention and community engagement.U.S.VETS is on a mission to end veteran homelessness in the United States. The organization was founded by veterans to serve fellow veterans and is the leading nonprofit dedicated to the work of helping veterans and their families transition from homelessness through tailored support to help them gain independence. Coinciding with U.S.VETS' 30th anniversary, the Congressional Medal of Honor Society awarded the organization its 2023 Community Service Award for demonstrating the values of courage, sacrifice, citizenship, integrity, commitment and patriotism embodied by the Medal of Honor. U.S.VETS is proud to be in the company of the exceptional individuals and organizations comprising this special brotherhood. U.S.VETS specifically in Hawai'i serves 850 veteran households annually throughout its programs and has been in existence since 2003.To reach U.S Vets Hawaii, you may contact them in the following ways:Phone: 808.630.0771Email: infohi@usvets.orgWebsite: usvets.org/

This week on the Team Lally Real Estate Radio Show, we interview Dr. Kim Cook and Tamah-Lani Noh from U.S Vets. We learn about their inspiring journey into veteran advocacy and how the U.S. Vets is leading the charge to end veteran homelessness. They highlight the critical services U.S. Vets provides, from housing and employment support to mental health services. We also hear exciting updates on their Tiny Homes project, which is open to both veterans and others in need. They explain how to connect with the U.S. Vets to explore housing and support options, and how you can get involved in their mission to make a real difference.We also have our Experts We Trust. Duke Kimhan from HI Pacific Property Management covers the importance of managing pests and termites in rental properties, highlighting the need for renters' insurance and addressing loss of rent during fumigation. Jodie Tanga from Pacific Rim Mortgage shares insights on current mortgage trends, explaining how inflation and market conditions are affecting rates and why today's rates are still better than last year.Who are Dr. Kim Cook and Tamah-Lani Noh?Dr. Kim Cook is the Vice President of Clinical Services at U.S. VETS. Born and raised on O‘ahu, she has dedicated her career to supporting veterans, overseeing programs that provide housing and care for nearly 850 veterans each night. She is a passionate advocate for holistic wellness and community service. Tamah-Lani Noh is a retired veteran with 30 years of service in the Hawai'i Air National Guard and U.S. Air Force. She's currently the Program Director and is known for her leadership in drug prevention and community engagement.U.S.VETS is on a mission to end veteran homelessness in the United States. The organization was founded by veterans to serve fellow veterans and is the leading nonprofit dedicated to the work of helping veterans and their families transition from homelessness through tailored support to help them gain independence. Coinciding with U.S.VETS' 30th anniversary, the Congressional Medal of Honor Society awarded the organization its 2023 Community Service Award for demonstrating the values of courage, sacrifice, citizenship, integrity, commitment and patriotism embodied by the Medal of Honor. U.S.VETS is proud to be in the company of the exceptional individuals and organizations comprising this special brotherhood. U.S.VETS specifically in Hawai'i serves 850 veteran households annually throughout its programs and has been in existence since 2003.To reach U.S Vets Hawaii, you may contact them in the following ways:Phone: 808.630.0771Email: infohi@usvets.orgWebsite: usvets.org/

Coinciding with Monocle's Quality of Life Conference in Istanbul, this week's Global Countdown sees Monocle Radio's Fernando Augusto Pacheco listen to some of the most important moments in Turkish pop history.See omnystudio.com/listener for privacy information.

Assassin's Creed Shadows has been delayed from November of this year to Feb. 14th 2025. In a statement posted to Twitter, the team cited the need to further polish and refine the experience, and to push some of its key features even further. Preorders for the game are being refunded, along with Ubisoft doing away with its traditional season pass model, allowing all future preorders to be given the first expansion for free. Remarking on this delay in a financial call, Ubisoft mentioned the learnings garnered from Star Wars Outlaws release, which led them to think about delaying Shadows to further tinker away at Shadows to make sure it is well polished and meets expectations. This is rather ambitious, giving us two distinct game styles with two unique protagonists you can play as in-game. Coinciding with this news, Ubisoft admits that Star Wars Outlaws didn't do so well. In the financial call, along with speaking on the delay of Assassin's Creed Shadow, Ubisoft spoke on changes it'll be making in response to player feedback on Outlaws to potentially garner a larger audience and potentially sustain the few that are still playing. And finally, we discuss Palworld's PS5 release worldwide, except for in Japan.

Coinciding with Kunsttage Basel, Meyer Riegger’s exhibition at Galerie Mueller honors the late Dutch artist Jacqueline de Jong (1939–2024), who ...

This week: the Van Gogh blockbuster in London, a new book on the birth of Impressionism, and Juan Pablo Echeverri's performative self-portraits. As the exhibition Van Gogh: Poets and Lovers opens at the National Gallery in London as part of its bicentenary celebrations, The Art Newspaper's special correspondent and resident expert in the Dutch painter, Martin Bailey, takes a tour of the exhibition with our associate digital editor, Alexander Morrison. The National Gallery of Art in Washington, meanwhile, has just opened the exhibition Paris 1874: The Impressionist Moment, its iteration of the show marking 150 years since the first Impressionist exhibition, which began earlier this year at the Musée d'Orsay in Paris. Coinciding with the show is the publication of the book Paris in Ruins: Love, War, and the Birth of Impressionism, by the Washington Post art critic, Sebastian Smee. Ben Luke speaks to Sebastian about the book. And this episode's Work of the Week is MUTIlady (2003) by Juan Pablo Echeverri. The photographic piece features nine photographs in which the late Colombian artist pictures himself with an apparently flayed body and wildly different haircuts seemingly reflecting a multitude of identities. The work is part of the exhibition GROW IT, SHOW IT! A look at hair from Diane Arbus to TikTok, which opened this week at the Museum Folkwang in Essen, Germany. The show's curator, Miriam Bettin, tells Ben more about the artist and the work.Van Gogh: Poets and Lovers, The National Gallery, London, 14 September-19 January 2025; The Sunflowers are Mine: The Story of Van Gogh's Masterpiece and Van Gogh's Finale: Auvers and the Artist's Rise to Fame by Martin Bailey, Frances Lincoln, each £10.99/$14.99 (pb), from 17 October, but available now at the National Gallery.Paris in Ruins: Love, War, and the Birth of Impressionism is published by W. W. Norton & Company in US and out now, priced $35. In the UK it's published by Oneworld, out on 17 October and priced £25; Paris 1874: The Impressionist Moment, National Gallery of Art, Washington, until 19 January 2025.GROW IT, SHOW IT! A look at hair from Diane Arbus to TikTok, Museum Folkwang, Essen, Germany, until 12 January 2025.Subscription offer: you can get the perfect start to the new academic year with 50% off a student subscription to The Art Newspaper—that's £28, or the equivalent in your currency, for one year. Visit theartnewspaper.com to find out more. Hosted on Acast. See acast.com/privacy for more information.

Coinciding with Kunsttage Basel, the second exhibition in Hauser & Wirth’s new Basel gallery is titled ‘Körperlich', meaning ‘bodily' in ...

Coinciding with the Torah Portion, Lech Lecha, which celebrates Abraham's choice to leave his ancestral home to become the father of monotheism and the Jewish People, we welcome Jason Hillman in this re-released episode. Mr. Hillman is currently serving as the Basketball Chief of Staff and Team Legal Counsel for the Cleveland Cavaliers. His decision to leave Detroit, his childhood home, to take a position in Cleveland with the Cavaliers was an opportunity and a personal reckoning. This open conversation may offer insight into our ability to take advantage when the world gives us the chance to do so. Join me as we chat about his choice to WAKE UP TO LIFE! If you enjoyed this episode, don't forget to subscribe and follow Temple Israel on social media to stay up to date on Waking Up To Life.    Facebook: https://www.facebook.com/templeisraelmi  Instagram: https://www.instagram.com/templeisraelmi/  YouTube: https://www.youtube.com/playlist?list=PLn9spWvsCBvcQ-o5XLeFLHKcLoj2nBAfM  Web: https://www.temple-israel.org/wakinguptolifepod 

In 2012, Oren Cass was the domestic policy advisor to Mitt Romney during his 2012 presidential campaign. Romney's economic policy epitomized that of the modern Republican Party: He celebrated free markets, free trade, and entrepreneurial capitalism. Since the time of Reagan, this worldview dominated the Right. But then, in the mid 2010s, something changed. An opioid crisis swept the Rust Belt, devastating communities that were thriving just decades ago. They suffered population decline, economic shrinkage, and the despair that accompanies both. This wasn't one small region experiencing this: It swept Ohio, Michigan, Wisconsin, Pennsylvania, upstate New York, West Virginia, Indiana, and Illinois. Even beyond the Rust Belt, working class towns and cities in every state saw factories close and workers lose their jobs. Coinciding with this trend was China's rise. China was the winner in this manufacturing shift. Whereas the United States was once the manufacturing leader of the world, China stole the crown in the mid 2010s and has put the United States in a $1+ trillion (!) trade deficit. In response to these changes, Oren Cass began publishing articles and writing the book "The Once and Future Worker." He then founded a think tank called the American Compass that makes the case for a worker- and community-first economic policy. He goes after Wall Street, Big Tech, and the neoliberal Washington, DC think tanks whose ideas shaped what he calls the "Old Right." He is one of JD Vance's major influences and has many disciples in Trump World. Some consider Cass to be the most important thinker of the New Right. So what does he believe? On this episode of We the 66, we talked to Cass and looked to find some answers. If you're curious, here is a link to Cass' new Substack: https://understandingamerica.substack.com/ For thoughts and feedback, email us at WeThe66@rocanews.com.

Fifteen years after starting his fashion brand, Jonathan Simkhai is still growing it — without financial help.  “The business is privately held, and we have not taken on any outside investment,” Simkhai said on the latest episode of the Glossy Podcast. “I am open to the idea, but we're also very happy just moving along and growing the business organically.” Coinciding with that growth has been the opening of four Simkhai stores — in Southampton, Beverly Hills, NYC's SoHo neighborhood and Dallas. There have also been marketing investments via global runway shows. This September, Simkhai will return to the New York Fashion Week runway, largely driven by customer demand.  "In our stores, I've heard so many clients say, 'Are you doing a show?' and 'We want to come to your show,'” he said. “In being so focused on the clients and meeting their needs and being there for them, I really want to do a show so I can have them there and give them that experience.” Also on the podcast, Simkhai discussed why he values time in his brand's stores, why specialty stores have an advantage over department stores and why experimentation is important to a modern fashion business. 

From today, new tax thresholds apply, which will reduce most people's income tax bills. Coinciding with the cuts is a ReliefAid campaign with a simple question: Will you give your tax cut to Gaza?

About the Guest(s): Dr. Kristin Hieshetter is an esteemed medical practitioner with a focus on functional health. Driven by her passion to improve public health and awareness, she combines extensive professional experience with a personal dedication to holistic wellness. Dr. Hieshetter is not only a leading voice in the field but also an advocate for incorporating nutritional and environmental considerations into healthcare. Her podcast, "Functional Health Radio," serves as a platform for educating the public on important health topics, providing practical advice, and inspiring meaningful changes in lifestyle and diet. Episode Summary: In this enlightening episode of Functional Health Radio, Dr. Kristin Hieshetter delves into the shocking decline in life expectancy in the United States, a trend that continues to affect both men and women. Coinciding with a rise in chronic illnesses among children, Dr. Hieshetter raises critical questions: Why is this happening, and how can we change it? She stresses the importance of recognizing the remarkable adaptability and intelligence of the human body and explores ways to unlock its true potential. Focusing on the impact of dietary choices, Dr. Hieshetter dissects the dangerous ingredients hidden in some of America's most popular packaged foods. From Cheetos and Oreos to Lays and Doritos, these products contain harmful chemicals, such as Monosodium Glutamate (MSG), that are banned in many countries due to their toxicity. Utilizing SEO-optimized keywords, Dr. Hieshetter highlights the potential damage these chemicals cause, including early onset puberty and brain cell damage, urging listeners to replace these with natural, healthier alternatives. Key Takeaways: Decline in Life Expectancy: The life expectancy in the US has dropped for both men and women, with chronic illnesses in children on the rise, highlighting a severe public health crisis. Toxic Chemicals in Food: Popular snacks are filled with harmful substances like MSG, disguised under various names, leading to severe health issues such as neurodegeneration and early puberty. Impact on Children: The younger the individual, the more damaging these chemicals can be, especially since they can cause long-term physiological and neurological harm. Holistic Dietary Choices: Emphasizing the importance of organic spices and natural foods, Dr. Hieshetter encourages moving away from processed snacks to protect our health and well-being. Empowering Change: Listeners are challenged to make small, impactful changes in their diet and to become advocates for better health in their communities. Notable Quotes: "We are walking around in the most amazing, intelligent, responsive, adapting, and aware system in the world, the human body." "Monosodium glutamate destroys your retina. It destroys it." "Your hypothalamus is like the control tower at an airport, regulating all the traffic." "Humans concentrate MSG in their blood better than any animal in these studies." "Let's say no to this garbage. Let's just do this. Enough is enough." Resources: While specific URLs are not mentioned in the transcript, the following references are implied for further exploration: Functional Health Radio on Apple Podcasts and Spotify. Books such as "Excitotoxins: The Taste That Kills" by Russell Blaylock. Various online resources about the health impacts of MSG and other food additives. Functional Health Mastery Embark on this eye-opening journey with Dr. Kristin Hieshetter to discover the hidden dangers in everyday foods and learn practical tips to enhance your and your family's health. Don't miss out on future episodes of Functional Health Radio for more transformative insights. Stay tuned!

Guy McAlester nearly gets struck and killed by car as he and his wife Agnes go to the store to load up for the Biden/Trump debate drinking game! THERE WERE NO WINNERS!ACTUAL AUDIO OF HOW A RIOT/ATTACK ON American democracy is incited! THIS IS AUDIO from all points of the square that day WHICH PROVES what Trump said was intentional and the effect it had on the anti-American crowd!

Chief Meteorologist Rich Wirdzek and Meteorologist Jake Grant talk this week about the first heat wave of the year. Coinciding with the bout of high heat, Rich and Jake look at the increasing dry conditions prompting a "flash drought" that's taking over much of the Mid-Atlantic, including here on Delmarva.

In this episode of Safety Shorts, Libby welcomes Sarah D'Amico, Marketing Manager of Turner Mining Group and Turner Staffing Group, to discuss the deeply personal importance of safety in such industries as mining. Sarah shares how her perspective on safety evolved from a set of rules to an emotional priority, particularly with her fiancé being a project superintendent in mining. Coinciding with Safety Month, Sarah's story underscores the life-changing consequences of neglecting safety measures as well as the importance of prioritizing workplace safety for everyone who cares for and counts on us. Episode Highlights: Sarah's initial unfamiliarity with the mining industry and how she approached safety from a logical standpoint Her relationship with her fiancé, who works in mining, and how it transformed her view on safety, making it an emotional priority The importance of safety training, reviewing national year-to-date fatalities, and the personal reflections that arise from these sessions The significant contributions of workers in trades and mining, and the importance of their safety The human stories behind safety statistics, emphasizing that every worker is crucial to someone Libby and Sarah encourage listeners to consider who they are being safe for and to continually prioritize safety in their daily routines Toolbox Talk Discussion Questions: In this episode, Sarah talks about how her perspective shifted and she started to look at safety as personal. Have you ever experienced this kind of shift, and why?  What do you think changes in our safety training when we shift our perspective to safety as personal?  Does anyone have a story about a loved one or family member working in the field? Key Takeaways: "Safety is one of our company's core values. It's ingrained in us to keep that top of mind." "You don't put yourself or others in danger. Be aware of your surroundings." "The ‘why' behind adhering to safety regulations is as important as the ‘how'." "'Everybody is somebody's everything.' This took on a very personal meaning for me." "Safety became much more of an emotional priority as opposed to pure logic." "Remind your coworkers: Who are you being safe for right now?" "Safety is not just about following SOPs but about protecting our families and those who rely on us." Links: National Stone, Sand & Gravel Association website Sarah D'Amico

This week on Pathfinder, we're joined by Jed McCaleb, Founder, and Max Haot, CEO, the leaders behind Vast, a company pioneering the development of commercial space stations. Jed, a seasoned software entrepreneur, and Max, a veteran in space and internet ventures, bring their unique expertise to the ambitious goal of advancing human habitation in space.Our conversation covers the critical aspects of creating economically viable space stations, the strategic role of life support systems, and the significance of reducing transportation costs. We also explore:Space station economics, pros/cons of competitionMilitary opportunities and sensitivities in space station useIntegration of Launcher post-acquisitionChallenges and excitement of Haven One's launchVast's product roadmapAnd much more… • Chapters •00:00 Intro00:53 Jed's career path and creating Vast02:57 Balancing aspirations and making money04:57 Max's history building business and how he came to Vast08:49 Max's primary objective at Vast11:22 Jed's experience building a hardware company12:31 Market opportunity for a free flying space station15:20 Haven 119:17 Building components in house21:07 Materials use and construction safety23:03 Vast's approach vs competitors29:45 Importance of being first in the market31:41 Is the market large enough to sustain multiple station providers?33:25 Common misconceptions of space station investment38:02 Vast x SpaceX partnership40:55 Product roadmap43:22 Coinciding with Starship timelines45:06 Will Starship be converted into a space station?46:10 Fundraising47:09 Economics around Haven 151:37 Military applications53:30 Utilization after acquisition54:13 What excites you and keeps you up at night?• Show notes •Max's socials — https://twitter.com/maxhaotJed's socials — https://twitter.com/JedMcCalebMo's socials — https://twitter.com/itsmoislamVast's website — https://www.vastspace.com/Payload's socials — https://twitter.com/payloadspace / https://www.linkedin.com/company/payloadspacePathfinder archive — Watch: https://www.youtube.com/@payloadspacePathfinder archive — Listen: https://pod.payloadspace.com/episodes • About us •Pathfinder is brought to you by Payload, a modern space media brand built from the ground up for a new age of space exploration and commercialization. We deliver need-to-know news and insights daily to 19,000+ commercial, civil, and military space leaders. Payload is read by decision-makers at every leading new space company, along with c-suite leaders at all of the aerospace & defense primes. We're also read on Capitol Hill, in the Pentagon, and at space agencies around the world.Payload began as a weekly email sent to a few friends and coworkers. Today, we're a team distributed across four time zones and two continents, publishing five media properties across multiple platforms:1) Payload, our flagship daily newsletter, sends M-F @ 9am Eastern2) Pathfinder publishes weekly on Tuesday mornings (pod.payloadspace.com)3) Polaris, our weekly policy briefing, publishes weekly on Tuesdays4) Payload Research, our weekly research and analysis piece,  comes out on WednesdaysYou can sign up for all of our publications here: https://payloadspace.com/subscribe/

In a shocking announcement on Wednesday, President Joe Biden revealed his administration's intent to halt the delivery of offensive weapons to Israel. This startling decision comes amid Israel's ongoing exertion on Rafah, a city to the southern edge of the Gaza Strip, to neutralize the lingering threats of the terrorism outfit, Hamas. Biden's decision has understandably led to a chorus of objections from Republicans, a fraction of Democrats, and former President Donald Trump, his prime political adversary. As reported by The Washington Post, a high-ranking official within the Biden administration revealed that the hold on weapons shipments is borne out of apprehensions over the consequences on civilian populations caught in the crossfire. The official expressed concerns over a potential large-scale ground operation by Israel in Rafah, a city where over a million people have taken refuge with minimal options for escape. The official went on record to underscore apprehensions specifically related to the use of the 2,000-pound bombs and their potential destruction in densely populated city settings, as witnessed in other regions of Gaza. The White House maintains that the administration's stance is dictated by humanitarian considerations as they assess the situation in the Middle East. Coinciding with these developments, Republicans, most notably the former President Trump, have been accusing Biden of succumbing to pressure from the far-left wing of his party. These factions of the Democratic Party have been known to advocate for a complete suspension of all US military support to Israel, a move that has been increasingly unpopular among more conservative factions.See omnystudio.com/listener for privacy information.

The dedicated team of the New York Police Department is seen demonstrating an exemplary level of respect for former President Donald Trump as they shield him from excessive media intrusions upon his daily trips to and from the courthouse in Manhattan. The New York Times inadvertently brought attention to the NYPD's 'preferential' treatment of Trump in their coverage. It's evident that Trump still holds a sense of regard in the books of the New York City Police Department. For the past week, there has been the unusual sight of a large police truck lodged at the meeting point of Hogan Place and Centre Street, staffed with a uniformed officer stationed inside. Coinciding with Trump's nearing arrival each day, the truck makes a slight progression closer to the courthouse, effectively obstructing the lens of news photographers attempting to capture his entry through the side door of the building. This particular activity, although seemingly mundane, by the NYPD is enacted not just in the mornings but also performed strategically during Trump's afternoon departures, around 2:37 p.m. This consistent treatment of Trump by NYPD doesn't seem to be just a random act of courtesy but rather a routine formed with a certain intent. The synchronistic relationship between the NYPD and Trump could be analyzed better in the light of recent events, especially Trump's attendance at a commemorative event in March. This memorial service was dedicated to an NYPD officer who tragically lost his life in the line of duty. Trump's appearance at this meaningful event was a symbolic act of respect and solidarity with the law enforcement community. This commemorative assembly coincided with the date of Joe Biden's indulgence in a lucrative fundraising event, attended by Barack Obama. The stark contrast in their agendas speaks volumes about their choices and priorities. While Trump honored police sacrifice, Biden and Obama pursued political funding, demonstrating potentially contrasting leadership styles. During Biden's leadership term, the country has been grappling with an ever-increasing crime rate along with the concerning phenomenon of 'migrant crime'. Trump, in a conversation with Breitbart News in March, drew attention to this new wave of crime plaguing the country. 'We're facing a new genre of crime in the United States, we can term it 'migrant crime', as he pointed out. 'Biden migrant crime' would be a more fitting terminology, but the phrase could be too tedious and frenzied for the masses. The increasing crime and the emergence of this new category of migrant crime are matters of real concern. Trump shed light on the intensity of these criminal acts, describing them as 'ferocious' and 'horrific'. The criminals are often perceived to be hardcore individuals, causing an atmosphere of fear and uncertainty. Trump has also highlighted that among the migrants coming into the country, many hold an unsavory reputation. The scales tilt heavily with a major share of these migrants being individuals with significant health issues, particularly mental health problems. Trump's straightforward statements reveal, without sugar-coating, the gravity of the situation. Contrary to popular discourse, Trump made 'law and order' a central tenet of his presidential terms in response to the nationwide upheaval witnessed in 2020. This was a bold move towards realigning the country's stance towards maintaining peace and order, signaling a shift towards a more organized and safer America. Trump's stance towards law and order didn't go unnoticed or unappreciated, as evidenced by the support he received from a sizeable extent of police and law enforcement groups. This backing was not merely in words but was also reflected in official endorsements Trump received throughout his presidential campaign over Biden. The Trump campaign reported an approximate figure of 900,000 officers offering their official endorsement to him during the 2020 election period. This number certainly points towards a significant inclination of the law enforcement community towards Trump, further reinforcing his image as a 'law and order' president. All in all, Trump's relationship with the law enforcement community, particularly the NYPD, and his stance on the pivotal issues facing the nation reflect his commitment towards reinforcing a safer, orderly America. Such visible displays of respect from the NYPD often go beyond mere courtesy and may reflect deeper bonds nurtured by shared values and mutual respect. While stories of 'preferential treatment' might foster intrigue amidst some quarters, it is essential to focus on the broader picture. The protection and respect accorded to Trump, as per this narrative, are presumably reflective not just of personal regard but also of the respect for the values he espoused. At a time of increasing pressing concerns like crime rates and migrant issues, it is such strong collaborative relationships between law enforcement and leaders which have the potential to instigate real change. With Trump's approach as an example, future leadership can take cues on the importance of maintaining strong, respectful ties with law enforcement bodies, advocating for law and order, and addressing nation-wide problems head-on. Real News Now Website Connect with Real News Now on Social Media Facebook: https://www.facebook.com/RealNewsNowApp/ X Twitter: https://twitter.com/realnewsapp Instagram: https://www.instagram.com/realnews/ TikTok: https://www.tiktok.com/@realnewsnowapp Threads: https://www.threads.net/@realnews/ Tumblr: https://www.tumblr.com/realnewsnow Truth Social: https://truthsocial.com/@RealNews YouTube:https://www.youtube.com/@realnewsnowapp End Wokeness: https://endthewokeness.com #realnewsnowSee omnystudio.com/listener for privacy information.

The 17-Foot Assassin, David West, joins the show to relive the rise of the New Orleans/Oklahoma City Hornets in the mid-2000's.West was drafted to the Hornets 18th overall in the legendary 2003 NBA Draft, joining the team for their first season in New Orleans. But just two years after West and the Hornets' arrival in New Orleans from Charlotte, they needed to move again due to the devastation of Hurricane Katrina. Just a month before the 2005/06 season tipped off, it was determined that Oklahoma City - who had no other major sports teams - would be the Hornets temporary home until New Orleans was rebuilt (enough).From 2005-2007, the Hornets played nearly all of their home games in Oklahoma City. And to their surprise, Oklahoma City welcomed them with rabid support. This successful foster parent-like relationship laid the groundwork for the city being able to swipe the Sonics from Seattle just a few years later.Coinciding with the Hornets temporary move to Oklahoma City was the emergence of the team, led by West and the young point god, Chris Paul. In 2008, the Hornets were back in New Orleans and won a franchise-record 56 games. They would fall to the Spurs in 7 games in the West Semis, and according to West, his injured back was the only thing that kept the Hornets from making the NBA Finals.West details the rapid ascension of his team, reveals the origin to his signature mid-range jump shot, gives his opinion to why the Hornets eventually fell apart and much more.Follow Forgotten Seasons (@forgottenseasonsnba) for more. Learn more about your ad choices. Visit megaphone.fm/adchoicesSee omnystudio.com/listener for privacy information.

The 17-Foot Assassin, David West, joins the show to relive the rise of the New Orleans/Oklahoma City Hornets in the mid-2000's. West was drafted to the Hornets 18th overall in the legendary 2003 NBA Draft, joining the team for their first season in New Orleans. But just two years after West and the Hornets' arrival in New Orleans from Charlotte, they needed to move again due to the devastation of Hurricane Katrina. Just a month before the 2005/06 season tipped off, it was determined that Oklahoma City - who had no other major sports teams - would be the Hornets temporary home until New Orleans was rebuilt (enough). From 2005-2007, the Hornets played nearly all of their home games in Oklahoma City. And to their surprise, Oklahoma City welcomed them with rabid support. This successful foster parent-like relationship laid the groundwork for the city being able to swipe the Sonics from Seattle just a few years later. Coinciding with the Hornets temporary move to Oklahoma City was the emergence of the team, led by West and the young point god, Chris Paul. In 2008, the Hornets were back in New Orleans and won a franchise-record 56 games. They would fall to the Spurs in 7 games in the West Semis, and according to West, his injured back was the only thing that kept the Hornets from making the NBA Finals. West details the rapid ascension of his team, reveals the origin to his signature mid-range jump shot, gives his opinion to why the Hornets eventually fell apart and much more. Follow Forgotten Seasons (@forgottenseasonsnba) for more. Learn more about your ad choices. Visit megaphone.fm/adchoices

The Allied Intervention into the Russian Civil War remains one of the most ambitious yet least talked about military ventures of the 20th century. Coinciding with the end of the first World War, some 180,000 troops from several countries including the United States, the United Kingdom, France, Japan, Italy, Greece, Poland, and Romania, among others, were sent to fight alongside Russian “Whites” against the Red Army.Despite one victory for the Allied troops – independence for the Latvians and the Estonians – the two-year long attempt at reversing the 1917 Russian Revolution ended in humiliating defeat. To explore this crucial event of the early 20th century is today's guest, Anna Reid, author of “A Nasty Little War: The Western Intervention into the Russian Civil War.”What was originally aimed to prevent Germany from exploiting the power vacuum in Eastern Europe left by the Russian Revolution ultimately morphed into the Allies' gamble to destroy Communist ideology. It was a mixture of good intentions and self-delusion, flag-waving and empty promises, cover-ups, exaggerations, and downright lies from politicians.

We pay tribute to another of the great labels of the O3L era...this time shining the spotlight on the magnificent DB Recs, the Atlanta-based label founded by Danny Beard, and run from 1978 - 1997 out of his still thriving record store Wax'n'Facts. Through Danny's ingenuity, support, and incredible ear for talent, it's safe to say that the alternative music scene in the Southeastern US would not be the same without him. DB's initial release was catalogue number DB-52, 'Rock Lobster' / '52 Girls', the first single by none other than The B-52's. From there, DB gave a voice to a wide range of artists in Atlanta, Athens, and beyond, including Pylon, Love Tractor, Oh-OK, Guadalcanal Diary, The Swimming Pool Q's, Fetchin Bones, Zeitgeist/The Reivers, The Jody Grind, The Coolies, Chris Stamey, and others. This week, we each offer up our Top 5 DB Recs songs with special guests Current Rage - John Moore (rhythm guitar), Paul Lenz (drums), and Bryan Lilje (bass). In absentia is lead guitarist and vocalist Olivia Bewley. You may remember the remarkable story of Current Rage from Episode 140: The band formed in 1979 by professional skateboarders Chris Bewley (brother of Pylon's Randy) and John Moore. By the beginning of 1981, they were headlining shows in the southeast with their brash, energetic, catchy post-punk tunes. They released the indie EP Seven Songs in 1982, which became a highly coveted collector's item among fans of DIY indie rock. After Current Rage ceased to be, each of the members followed different paths, with Chris Bewley succumbing to a heart attack in 2018 at the age of 57. Coinciding with the expanded 40th anniversary reissue of Seven Songs in 2022 on Propeller Sound Recordings, Current Rage is now back and experiencing a resurgence...with a twist. Chris's daughter Olivia plays lead guitar and sings in the current iteration of the band. While she never had much of a relationship with her father, through his music, his former band, and even some of his equipment, she is able to connect with Chris in powerful, unexpected ways. During this episode, we catch up with the band and (despite not being DB Recs artists themselves) discuss the indelible impact of Danny Beard and the DB roster on them. Deep gratitude to Current Rage's manager, Robin Hall Bewley Frankland, for organizing this return visit to O3L! Learn more about your ad choices. Visit megaphone.fm/adchoices

We pay tribute to another of the great labels of the O3L era...this time shining the spotlight on the magnificent DB Recs, the Atlanta-based label founded by Danny Beard, and run from 1978 - 1997 out of his still thriving record store Wax'n'Facts. Through Danny's ingenuity, support, and incredible ear for talent, it's safe to say that the alternative music scene in the Southeastern US would not be the same without him. DB's initial release was catalogue number DB-52, 'Rock Lobster' / '52 Girls', the first single by none other than The B-52's. From there, DB gave a voice to a wide range of artists in Atlanta, Athens, and beyond, including Pylon, Love Tractor, Oh-OK, Guadalcanal Diary, The Swimming Pool Q's, Fetchin Bones, Zeitgeist/The Reivers, The Jody Grind, The Coolies, Chris Stamey, and others. This week, we each offer up our Top 5 DB Recs songs with special guests Current Rage - John Moore (rhythm guitar), Paul Lenz (drums), and Bryan Lilje (bass). In absentia is lead guitarist and vocalist Olivia Bewley. You may remember the remarkable story of Current Rage from Episode 140: The band formed in 1979 by professional skateboarders Chris Bewley (brother of Pylon's Randy) and John Moore. By the beginning of 1981, they were headlining shows in the southeast with their brash, energetic, catchy post-punk tunes. They released the indie EP Seven Songs in 1982, which became a highly coveted collector's item among fans of DIY indie rock. After Current Rage ceased to be, each of the members followed different paths, with Chris Bewley succumbing to a heart attack in 2018 at the age of 57. Coinciding with the expanded 40th anniversary reissue of Seven Songs in 2022 on Propeller Sound Recordings, Current Rage is now back and experiencing a resurgence...with a twist. Chris's daughter Olivia plays lead guitar and sings in the current iteration of the band. While she never had much of a relationship with her father, through his music, his former band, and even some of his equipment, she is able to connect with Chris in powerful, unexpected ways. During this episode, we catch up with the band and (despite not being DB Recs artists themselves) discuss the indelible impact of Danny Beard and the DB roster on them. Deep gratitude to Current Rage's manager, Robin Hall Bewley Frankland, for organizing this return visit to O3L! Learn more about your ad choices. Visit megaphone.fm/adchoices

6PM ET 02/20/2024 Newscast Learn more about your ad choices. Visit megaphone.fm/adchoices

We had the pleasure of interviewing Jagwar Twin over Zoom video!Deemed by many as the unofficial anthem of the " Wonka" soundtrack, Jagwar Twin has officially entered the new year with a lyric video for the massive hit, "Bad Feeling (Oompa Loompa) ". Weaving together candycoated harmonies and whimsical instrumentals, the track epitomizes Jagwar Twin's distinctive musical prowess that effortlessly balances nostalgia and fresh innovation.With over 40 million views across TikTok and 8 million streams in less than a month, Jagwar Twin's latest electrifying single has taken the digital music scene by storm, achieving remarkable success on TikTok and playlists alike. The track's infectious beats and catchy lyrics have sparked various viral trends on TikTok, where users from around the globe have embraced the song with over 150K user-created videos using the track, securing Jagwar Twin a spot on TikTok's Viral 50 Chart. Simultaneously, " Bad Feeling (Oompa Loompa)" has found its place on influential playlists across streaming platforms, including the coveted covers of not only Spotify's The New Alt and Limelight, but Amazon Music's DV8. This dual triumph highlights Jagwar Twin's innate ability to connect with diverse audiences and solidifies the track as a dynamic force in the contemporary music landscape.Coinciding with the release of Paul King's "Wonka", “Bad Feeling (Oompa Loompa) ” features an interpolation of “ Oompa Loompa", marking a rare approval from the original film's composers. Delving into the world of Willy Wonka, Jagwar Twin brings a new life and twist to the classic "Oompa Loompa" chorus, while also modernizing it. Co-written by Sean Van Vlee t (All Time Low, PVRIS) and Ryan Daly (Dove Cameron, John Legend), "Bad Feeling (Oompa Loompa) ", exemplifies the magic of modern visionaries reimagining the timeless charm of musical classics."Bad Feeling (Oompa Loompa)" is similar in style to his previous release, “ Good Time (1:08)”, which peaked Top 20 at Mexico radio, and stand out track “Happy Face.” With an impressive 425+ million catalog streams and 2.5 million monthly listeners on Spotify, Jagwar Twin stands out as a dynamic force challenging the status quo of the alternative music scene . His genre-defying artistry has captivated audiences through the seamless blend of rhythmic accordion hooks, melodic children's choirs, and gritty breakbeats, accompanied by profoundly introspective, almost cryptic lyrics.Jagwar Twin's previous album, 33, channeled the magnetic showmanship of Ziggy Stardust -era David Bowie and Bad -era Michael Jackson, all while unapologetically embracing authenticity and vulnerability. Fueled by chart-toppers like "It's Your Time," "I Like To Party," "Down To You," and "Happy Face," Jagwar Twin serves as a powerful catalyst. His innovative style urges listeners to embrace their true selves, recognize their self-worth, and place trust in their individuality.We want to hear from you! Please email Hello@BringinitBackwards.comwww.BringinitBackwards.com#podcast #interview #bringinbackpod #JagwarTwin #NewMusic #ZoomListen & Subscribe to BiBhttps://www.bringinitbackwards.com/followFollow our podcast on Instagram and Twitter! https://www.facebook.com/groups/bringinbackpod

The people are showing up and calling in today. Howie gets on-the-ground photos from outside the Harvard doxxing truck, where pro-Palestine pampered pukes are picketing. Shouldn't they be in class? Then, a man calls in to explain how he's being kicked out of his long-term hotel stay. Turns out, illegal aliens (the government) are willing to pay more!