Angela Walker In Conversation - Inspirational Interviews, Under-Reported News

Artificial Intelligence has rapidly integrated into our daily lives, becoming an essential tool across healthcare, transportation, and communication. However, a critical question emerges: is AI inherently biased? This question forms the cornerstone of a fascinating conversation with Christian Ortiz, founder of Justice AI – the world's first ethical AI system specifically designed to address and correct biases rooted in historical inequities.The fundamental issue with AI, as Ortiz explains, stems from the data it processes. AI systems learn from vast datasets that predominantly contain Eurocentric ideologies and perspectives. As a decolonial technologist, he has observed how these systems perpetuate biases originating from settler colonialism and structures of discrimination that have been systematically embedded in Western societies.Ortiz argues that these biases have real-world implications. He shares a powerful example from his work with a dermatologist in Denver who, realized his medical forms and diagnostic approaches were failing patients of color. When Justice AI analysed the intake forms, it revealed they were based entirely on Eurocentric diets and cultural assumptions, missing crucial information needed to properly diagnose and treat patients from different cultural backgrounds. The development of Justice AI involved collaboration with over 560 marginalised individuals from diverse backgrounds around the world, each bringing approximately 30 years of knowledge to the dataset. This collective expertise forms the foundation of an AI system designed to counterbalance the biases present in mainstream AI platforms like ChatGPT.Listen now, to find out more.https://justiceai.co/It's not possible to reply to “fan mail” so please contact me through my website angelawalkerreports.com Support the showhttps://www.angelawalkerreports.com/

The culture of cover-up within British public institutions has devastated countless lives. From Hillsborough to the infected blood scandal to the Primodos drug tragedy, families have spent decades fighting for truth against a system where many in authority have colluded against them.This episode explores the urgent need for the Public Authority Accountability Bill - commonly known as Hillsborough Law - with two powerful voices leading the charge: Andy Burnham, Mayor of Greater Manchester who first introduced the bill to Parliament in 2017, and Marie Lyon, Chair of the Association for Children Damaged by Pregnancy Hormone Tests.The bill would establish a legal duty of candour with criminal sanctions for officials who mislead or obstruct investigations. Equally crucial, it would ensure parity of legal funding at inquests, stopping the practice where public bodies hire top legal representation while families struggle with limited resources. As Burnham explains, "It has been too easy for authorities to cover up in this country and too hard for ordinary families to get to the truth."Marie Lyon shares the harrowing story of how pregnant women were prescribed Primodos - a drug containing synthetic hormones at 40 times the dose in contraceptive pills - despite evidence dating back to 1967 showing it caused birth defects. The decades-long cover-up reveals a disturbing pattern: public bodies prioritising financial considerations over human suffering.Despite Prime Minister Keir Starmer's commitment to enact the law before the 36th anniversary of Hillsborough, the deadline has passed. Campaigners remain vigilant against attempts to water down the legislation."The British government underestimates the strength of the British people because people do not give in and they keep fighting." says Burnham. https://hillsboroughlawnow.org/https://primodos.org/It's not possible to reply to “fan mail” so please contact me through my website angelawalkerreports.com Hi listener. I thought you might enjoy Don Anderson's podcast. Missing Pieces - NPE Life is a podcast that curates stories of and about people who find out, usually through a home DNA test, that someone in their family tree isn't who they thought. They also tell stories of adoptees who've found lost family, or are looking. The host, Don Anderson, found out in 2021 that his dad wasn't his dad. It changed his life. NPE stands for Not Parent Expected or Non Paternity Event.Support the showhttps://www.angelawalkerreports.com/

Send us a textA Canadian inventor successfully adapted a car to run on ammonia 40 years ago. Why did governments suppress this technology? Greg Vezina shares how ammonia could finally lead us to a hydrogen economy without building entirely new infrastructure.His journey began with a single car conversion in the 1980s that sparked four decades of advocacy for ammonia as a cleaner energy alternative. The chairman and CEO of Hydrofuel Canada shares how he successfully adapted a Chevrolet Impala to run on ammonia and drove it across Canada, only to face political roadblocks despite demonstrating the technology's viability.The most promising immediate applications for ammonia aren't personal vehicles but industrial sectors—cement production, heavy equipment, garbage collection, and shipping. Projects like the UK's Leeds initiative, with offshore wind generators producing ammonia on-site to fuel barges, demonstrate practical integration with existing systems.Beyond ammonia, Vezina's team is pioneering photochemistry—using light instead of heat for chemical processes—which could revolutionise hydrocarbon refining without carbon emissions. This breakthrough would allow continued use of existing infrastructure while eliminating pollution, offering a pragmatic transition pathway.Want to learn more about the future of clean energy? Visit hydrofuel.com and follow the developments being announced at the Canadian Hydrogen Conference. The energy revolution may not look exactly as we imagined—it might be powered by ammonia instead.Hi listener. I thought you might enjoy Don Anderson's podcast. Missing Pieces - NPE Life is a podcast that curates stories of and about people who find out, usually through a home DNA test, that someone in their family tree isn't who they thought. They also tell stories of adoptees who've found lost family, or are looking. The host, Don Anderson, found out in 2021 that his dad wasn't his dad. It changed his life. NPE stands for Not Parent Expected or Non Paternity Event.Support the showhttps://www.angelawalkerreports.com/

Send us a textMany young disabled adults are not fulfilling their potential because of a lack of government support. That's according to the founder of a charity that helps those young people achieve their ambitions. Jane Holmes set up Building for the Future because of her own experiences after her daughter, Kitty, was born 24 years ago. Building for the Future supports around 500 families but is running out of space and plans to expand by 2026 to better serve young adults transitioning from education. These young people often face isolation when care packages prove insufficient, leading parents in their 50s to abandon careers to provide necessary support. With the charity receiving no government funding and concerns about proposed cuts to disability benefits, Jane calls for longer-term thinking from policymakers.https://www.bftf.org.uk/Hi listener. I thought you might enjoy Don Anderson's podcast. Missing Pieces - NPE Life is a podcast that curates stories of and about people who find out, usually through a home DNA test, that someone in their family tree isn't who they thought. They also tell stories of adoptees who've found lost family, or are looking. The host, Don Anderson, found out in 2021 that his dad wasn't his dad. It changed his life. NPE stands for Not Parent Expected or Non Paternity Event.Support the showhttps://www.angelawalkerreports.com/

Send us a textImagine being selected to represent your country, to compete against the best in the world - and then needing to find the money to pay for it your self.Tamina Oliver is a single mum from Twyford in Berkshire whose journey into elite duathlons is riddled with challenges and triumphs. Tamina shares her experience of qualifying for the European and World Championships, all while overcoming significant injuries and the struggle to find sponsorship. In this conversation Tamina shares her journey through motherhood and injury and tells us how she balances rigorous training with parenting duties, waking up early to fit in workouts before the school run, and even cycling with her son in tow. Tamina honestly discusses the frustrations tied to the financial barriers that threaten her ability to compete. This episode invites you to explore the realities faced by elite athletes, particularly women, in their pursuit of excellence. Tamina's commitment to her sport is a powerful reminder of the importance of community support and the lengths to which dedicated athletes will go to pursue their dreams. If you have ever faced challenges in following your passions, this conversation will resonate deeply with you. https://www.crowdfunder.co.uk/p/gb-duathlon-dream-world-champs-2025Support the showhttps://www.angelawalkerreports.com/

Send us a textSynthetic chemicals which can cause cancer are contaminating our drinking water and farmland, and have been found in breast milk and embryos. Why is the British government so slow to regulate against them? Why are higher levels of polyfluoroalkyl substances allowed in our drinking water than in other countries?They're in many products including noon-stick pans and fire-fighting foam - but there are alternatives.My guest is Environmental Journalist Leana Hosea and co-founder of Watershed Investigations.https://watershedinvestigations.com/https://www.angelawalkerreports.com/Hi listener. I thought you might enjoy Don Anderson's podcast. Missing Pieces - NPE Life is a podcast that curates stories of and about people who find out, usually through a home DNA test, that someone in their family tree isn't who they thought. They also tell stories of adoptees who've found lost family, or are looking. The host, Don Anderson, found out in 2021 that his dad wasn't his dad. It changed his life. NPE stands for Not Parent Expected or Non Paternity Event.Support the showhttps://www.angelawalkerreports.com/

Send us a textWhat effect will Donald Trump's crackdown on diversity have on the UK?He's scrapping all the government's Diversity, Equity and Inclusion programmes and sent all the staff home.Diversity isn't just about compliance—it's about transforming workplaces and societies - that's the view of Mo Kanjilal, a leading voice in diversity and inclusion.Join me, journalist Angela Walker, as I sit down with Mo to investigate the ripple effects of Donald Trump's policies on both sides of the Atlantic. We unpack the rollback of diversity programs and protections for marginalised groups, exploring how these actions might shape corporate cultures in the UK and feed into broader societal attitudes. Mo sheds light on the root causes of resistance to diversity, often born out of fear and misunderstanding, while also addressing the persistent challenges and discrimination faced by women and minorities in professional settings. Our conversation extends to the alarming rise of racism, fuelled by international rhetoric, stressing the urgency of fostering inclusive environments.https://www.watchthisspace.uk/https://www.amazon.co.uk/Inclusion-Journey-Creating-strategy-engagement/dp/1398616729/#DiversityAndInclusion#EquityMatters#InclusionJourney#DiversityAtWork#BreakingBarriers#MoKanjilal#TransformingWorkplaces#InclusionMatters#EndDiscrimination#WomenInLeadership#DiversityUnderAttack#TrumpPolicies#GlobalImpact#RacismAwareness#SocialJustice#InclusiveFuture#StandForChange#MakeWorkplacesInclusive#FearVsUnderstanding#EqualityForAllHi listener. I thought you might enjoy Don Anderson's podcast. Missing Pieces - NPE Life is a podcast that curates stories of and about people who find out, usually through a home DNA test, that someone in their family tree isn't who they thought. They also tell stories of adoptees who've found lost family, or are looking. The host, Don Anderson, found out in 2021 that his dad wasn't his dad. It changed his life. NPE stands for Not Parent Expected or Non Paternity Event.Support the showhttps://www.angelawalkerreports.com/

Send us a textIn this conversation, John Cardamone shares his personal journey of healing from childhood abuse and explains how he helps families, schools and organisations create better connections with children, so they are happy and confident - and able to confide if things go wrong.John explains how his mum's reaction when he disclosed be was being abused by a family member was critical in enabling him to get help and recover.He discusses the importance of accountability for abusers and the societal responsibility to address child sexual abuse effectively, in the light of the Church of England scandal that saw the resignation of Justin Welby, the Archbishop of Canterbury who failed to report prolific child abuser John Smyth to police.John highlights his coping mechanisms, including the significance of connection and belonging, and introduces practical tools for families to communicate about body safety and empower children. The discussion underscores the need for a shift in societal attitudes towards child abuse and the importance of creating safe spaces for children to express themselves.https://johncardamone.com.au/https://www.nspcc.org.uk/Hi listener. I thought you might enjoy Don Anderson's podcast. Missing Pieces - NPE Life is a podcast that curates stories of and about people who find out, usually through a home DNA test, that someone in their family tree isn't who they thought. They also tell stories of adoptees who've found lost family, or are looking. The host, Don Anderson, found out in 2021 that his dad wasn't his dad. It changed his life. NPE stands for Not Parent Expected or Non Paternity Event.Support the showhttps://www.angelawalkerreports.com/

Send us a textIt's 20 years since the Boxing Day tsunami in the Indian Ocean that killed more than 200,000 people.Londoner Ani Naqvi was asleep in a beach hut in Sri Lanka when the tsunami hit, filling the hut with water and almost drowning her.In this podcast Ani shares her life before the tsunami, the harrowing experience of the disaster, and the profound impact it had on her life. She discusses her struggles with PTSD, her journey towards healing, and how she found purpose in helping others after surviving such a traumatic event. The conversation delves into themes of survival, personal growth, spirituality, and the search for meaning in the aftermath of tragedy.https://shopbooksdirect.com/product/tsunami-the-wave-that-saved-my-life-and-can-save-yours/Support the showhttps://www.angelawalkerreports.com/

Send us a textAdults with learning difficulties are being moved out of their homes against their wills - with some ending up in secure accommodation.Around forty "villages" have been shut down over the past few years and many residents face problems finding suitable housing.Campaigners say adults with learning difficulties and their families are not being listened to.In this conversation, journalist Angela Walker speaks with Ron Brown from the charity Our Life, Our Choice about the pressing need for more choice and better accommodation options for adults with learning disabilities. They discuss the challenges faced by individuals in finding suitable living arrangements, the role of regulatory bodies, and the importance of advocacy and community involvement in ensuring that the voices of those affected are heard.Music credit: Moment of Inspiration by Purple Planet Musichttps://ourlifeourchoice.co.uk/Support the showhttps://www.angelawalkerreports.com/

Send us a textWhen Gaia Young arrived at hospital confused, vomiting and complaining of a severe headache, it was assumed she was drunk or on drugs.She wasn't.The 25 year-old from London died from swelling to the brain. But what caused it? In this podcast Angela Walker talks to Gaia's mother Lady Dorit Young about her relentless campaign for answers to her daughter's death.Was it an unavoidable tragedy, or the result of systemic failures? Could Gaia have been saved if her illness was treated differently? Why were crucial and routine tests not carried out, and could they have saved her life? Why did the inquest leave more questions than answers?https://truthforgaia.com/Support the showhttps://www.angelawalkerreports.com/

Send us a textInstitutional racism, socio-economic factors and low aspirations from teachers  are causing boys of Caribbean descent to fail in school.That's the view of founder of The Westside and Lewisham Young Leaders Academies, by David Okoro.Children of black Caribbean descent face significant educational disparities, with lower achievement in GCSE, higher rates of exclusion and are more likely to end prison. The academies offer a range of programmes, including mentoring, leadership development, and exposure to successful black role models to raise confidence, aspirations, and skills among black youths. In this podcast David Okoro and Chidera Nomeh, a student at Westside Academy join Angela Walker to talk about the positive impact of the academies and to discuss the wider issue of what can be done to close the gap.The academies face funding challenges and rely on grants, donations, and volunteers to continue their work. David emphasises the need for government intervention and investment to address the systemic issues contributing to the underachievement of black young people.https://www.wylauk.com/Music credit: Moment of Inspiration by Purple Planet MusicSupport the showhttps://www.angelawalkerreports.com/

Send us a textWhat would you do if your child died as a result of medical negligence and doctors and the police colluded to cover it up? That's what happened in the case of ten-year-old Robbie Powell.His parents are campaigning for all healthcare professionals to be legally obligated to tell the truth following a negligent death. They're supported by the former Parliamentary Health Service Ombudsman Sir Rob Behrens CBE  says: "Mr Powell was personally traduced by doctors, by regulators by the police service, by the Crown Prosecution Service, by politicians in a way which is just unacceptable. He was patronised and he never gave up." Robbie died from Addison's Disease. He could have been saved if  doctors had carried out the necessary tests and informed the family of the risks. Instead, numerous medics failed him and spent 30 years covering it up.In this podcast Robbie's father Will Powell and Sir Rob Behrens join me to discuss the Powell family's relentless pursuit of truth and justice and the systemic failures that have deprived his family of justice for more than 30 years. Support the showhttps://www.angelawalkerreports.com/

Send us a Text Message.Racists are on the rampage in the UK, with over 100 far-right protests planned later today. I talk to Leroy of Caribbean heritage and Mo whose Indian family were immigrants about the impact of these attacks on their communities and the country as a whole. We discuss the historical context of racism in the UK and the need for accountability in the media and social media platforms. We also talk about the trauma and identity crisis caused by these events and the importance of standing up against racism. The conversation touches on the role of politicians, the police, and the need for swift action to address the spread of misinformation and protect vulnerable communities.Support the Show.https://www.angelawalkerreports.com/

Send us a Text Message.Thousands of patients were lied to and given blood products that infected them with HIV and Hepatitis.Doctors knowingly infected hundreds of children and then covered it up. @AngelaWalkerReportsInterviews  Medical professionals and politicians put vulnerable patients at "unacceptable risk" the UK"s Infected Blood Inquiry report has found.More than 30,000 people were infected with contaminated blood products administered by the NHS in the 1970s and 80s.Join Angela Walker for a compelling, powerful and emotional discussion with Clive Smith, Chair of the Trustees of the Haemophilia Society, as we uncover the profound implications of the Infected Blood Inquiry's final report. Sir Brian Langstaff's  findings reveal a scandalous decision in 1973 to license contaminated blood products, leading to preventable infections and a shocking cover-up by both medical professionals and government officials. Clive shares the deep personal and communal impact of this health crisis, emphasizing the conspiracy to conceal the truth and the failure to protect patients.The episode delves into the government's controversial response to the reports from Sir Robert Francis and Sir Brian Langstaff concerning victim compensation. Listeners will hear about the skepticism surrounding the government's rapid overnight response, the unprecedented measures taken to ensure accountability, and the ongoing political complexities, including the calling of a general election. We also address the emotional toll on the affected community and the significance of an effective compensation scheme for the victims and their families.Angela and Clive reflect on the historical context of the contaminated blood scandal, highlighting the political and administrative failures that perpetuated this tragedy. The conversation covers the harrowing experiences of those living with hemophilia, the tragic stories of co-infections with HIV and hepatitis C, and the broader systemic failures that allowed this disaster to occur. This episode is a testament to the resilience of the victims and their unwavering commitment to justice and patient safety.https://www.angelawalkerreports.com/Support the Show.https://www.angelawalkerreports.com/

Send us a Text Message.Two million scientific experiments were carried out on animals in the UK in 2022.More than four thousand Beagles were among them.Home office figures published in April 2024 show that  in 2022 there were 175 cases of non-compliance to government regulations regarding the welfare of animals used in testing. More than  16,000 animals were affected. The government is promising to investigate.MBR Acres in Cambridgeshire is a puppy farm, where beagles are bred to be tested on with toxic chemicals.Campaigners say the practice is cruel, outdated and unnecessary. Proponents argue animal tests are essential for the advancement of science.Outside MBR Acres is an encampment of protesters who have lived at the site for almost three years. John Curtin is one of them. He explains how they obtained footage inside the top security site - and how he's been arrested for flying a small drone over the site.John tells us how he has seen hundreds of vans carrying dogs from site, which they have followed across the UK to their final destinations - science laboratories.  He shares stories of animal rights group Animal Rising who have broken into the site and freed a number of dogs.I invited the following parties to participate in the podcast or provide a comment. They did not.MBR AcresMinister for Science, Research and Innovation, Andrew GriffithProfessor David Main, Chair of the Animals in Science CommitteeMP for Huntingdon, Jonathan DjanoglyMP for North West Cambridgeshire, Shailesh Vara https://thecampbeagle.com/https://www.animalrising.org/https://www.gov.uk/government/publications/animal-testing-debate-letter-to-andrew-griffith/animal-testing-debate-letter-to-andrew-griffith-accessiblehttps://www.criver.com/about-us/about-us-overview/animals-research?region=3696Support the Show.https://www.angelawalkerreports.com/

Send us a Text Message.Around 100,000 people in the UK are living with HIV.75% of them say they face discrimination because of it. Why is that and what can be done about it? In this podcast episode, journalist Angela Walker interviews Matthew Hodson, Executive Director of the charity aidsmap about the stigma surrounding HIV and what can be done to address it. Matthew shares his personal story of being diagnosed with HIV in 1998 and discusses the progress that has been made in HIV treatment and life expectancy. He emphasises the importance of education and dispelling myths about HIV, as well as the need for positive role models and support for people living with HIV. The conversation also touches on the global stigma of HIV and the work of aidsmap in providing information and support.Takeaways:Stigma surrounding HIV still exists, but progress has been made in terms of treatment and life expectancy.Education and dispelling myths about HIV are crucial in addressing stigma.Positive role models and support for people living with HIV are important in changing perceptions.Visit the AIDSMAP wesbite:  https://www.aidsmap.com/Support the Show.https://www.angelawalkerreports.com/

Imagine going in for routine day surgery to help stop occasional bladder leaks and being left permanently disabled needing a wheelchair or stoma bag. That's what's happened to thousands of women around the world.When Kath Sansom of Sling the Mesh began her campaign, she never imagined it would resonate with so many. This episode brings Kath's emotional account of her personal struggles with pelvic mesh complications, revealing the depths of a medical disaster that has left countless lives in turmoil and even led some women to take their own lives.The conversation with Kath is both enlightening and heart-wrenching, as she discusses not only her own journey—from the debilitating aftermath of surgery to her powerful activism—but also the shared narratives of women facing similar battles.The physical and psychological scars left by mesh surgeries are profound . We delve into how these medical procedures have drastically altered lives, leaving individuals grappling with chronic pain, loss of mobility, and an array of systemic health problems and an inability to have sex leading to marriage breakdowns. Kath's insights into the ongoing fight for recognition, the quest for justice, and the stark increase in dependency on medications are eye-opening. This episode is an earnest exploration of the human cost of a healthcare crisis, shedding light on the resilience and determination of those who have been affected.Join us as we discuss the urgent need for financial redress and transparency in the healthcare system, and Kath's calls a  Sunshine Payment Act. We touch on  the stark differences in responses across the globe. Kath's advocacy work with Sling the Mesh provides a beacon of support, offering resources for anyone affected by mesh. This episode is more than a conversation; it's a call to awareness and empathy for the victims of a widespread medical oversight that demands our attention and action.Support the showhttps://www.angelawalkerreports.com/

A look forward to upcoming stories in the series Angela Walker in Conversation with topics ranging from animal testing to medical negligence.And a reminder of some of the stories we've covered so far -  including disability discrimination and environmental destruction.Also, how you can get involved and support independent journalism.Support the showhttps://www.angelawalkerreports.com/

Body image concerns related to weight and appearance are now prevalent on a global scale, leading to widespread mental health pressures. This conversation explores the topics of body image, self-acceptance, and the impact of social media and advertising on our perception of beauty. Alexandra Vince, a boudoir photographer, shares her journey and how her work empowers women to feel confident in their bodies. Kate Richmond, who underwent weight loss and corrective surgery, discusses her struggles with body image and the importance of self-acceptance. The conversation highlights the need to embrace our bodies as a whole and challenge societal beauty standards.We discuss how body image concerns are prevalent on a global scale and can lead to mental health pressures and what could be done. Kate reveals her battle for self-acceptance and opens up about her weigh, how she lost several stone and the effect it had on her self-perception. Alex explains how photography can play a role in empowering women and helping them feel confident in their bodies.https://www.fyeoboudoirphotography.com/a-day-in-the-life-of-leading-boudoir-photographer-alexandra-vince/https://publications.parliament.uk/pa/cm5803/cmselect/cmhealth/114/report.htmlhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9970735/Support the showhttps://www.angelawalkerreports.com/

Bite size. Full length version available.Bottom trawling is a destructive fishing method that indiscriminately catches everything in its path, causing damage to the seabed and releasing carbon. Over the past 150 years, bottom trawling has depleted fish populations and harmed marine biodiversity. Efforts have been made to mitigate the impact of bottom trawling through the establishment of marine protected areas and the development of more selective fishing gear. However, the recovery of fish populations and the restoration of the seabed will take time. It is important for consumers to be informed about the fishing methods used and to support environmentally friendly fishing practices.In this podcast I talk to Dr Jean-Luc Solandt, Principal Specialist in Marine Protected Areas at the Marine Conservation Society.Marine Conservation Society:  https://www.mcsuk.org/Pictures courtesy of www.skytruth.org#BottomTrawling#FishingImpact#MarineConservation#SustainableFishing#ProtectOurSeas#OceanHealth#MarineBiodiversity#EcoFriendlyFishing#FisheriesManagement#EnvironmentalAwareness#SeabedDamage#SelectiveFishing#ConservationEfforts#MarineProtection#FishPopulationRecoverySupport the showhttps://www.angelawalkerreports.com/Support the showhttps://www.angelawalkerreports.com/

95 percent of fish stocks in the North Sea have been depleted due to over-fishing and bottom trawling. @AngelaWalkerInConversati-yc1rc  Bottom trawling is a destructive fishing method that indiscriminately catches everything in its path, causing damage to the seabed and releasing carbon. Over the past 150 years, bottom trawling has depleted fish populations and harmed marine biodiversity. Efforts have been made to mitigate the impact of bottom trawling through the establishment of marine protected areas and the development of more selective fishing gear. However, the recovery of fish populations and the restoration of the seabed will take time. It is important for consumers to be informed about the fishing methods used and to support environmentally friendly fishing practices.In this podcast I talk to Dr Jean-Luc Solandt, Principal Specialist in Marine Protected Areas at the Marine Conservation Society.Marine Conservation Society:  https://www.mcsuk.org/Pictures courtesy of www.skytruth.org#BottomTrawling#FishingImpact#MarineConservation#SustainableFishing#ProtectOurSeas#OceanHealth#MarineBiodiversity#EcoFriendlyFishing#FisheriesManagement#EnvironmentalAwareness#SeabedDamage#SelectiveFishing#ConservationEfforts#MarineProtection#FishPopulationRecoverySupport the showhttps://www.angelawalkerreports.com/

Jim Smith has sold  one million children's books and his graphic novels inspire children all over the world who might otherwise not pick up a book. He won the Roald Dahl Funny Prize in 2013 for his second book “I am still not a Loser” and the second book in the spin-off series Future Ratboy won The Laugh Out Loud Children's Book Awards in 2017 for 6–8-year olds.In this World Book Day special,  we discuss Jim's journey as an author, the inspiration for his characters and doodles, and the story behind his most famous creation Barry Loser.  We ask why kids find Jim's book so funny - and Jim reveals his tips for aspiring graphic novelists. Jim explains how he got started designing the packaging for the coffeeshop chain Puccino Coffee. He's also the illustrator and designer behind the gift and card range, Waldo Pancake.Plus, there's a special guest appearance by one of Jim's greatest fans and a sneak peek at two new books which are out in a few months time.https://uk.bookshop.org/shop/jimsmithSupport the showhttps://www.angelawalkerreports.com/

The UK is in the middle of a chronic housing shortage. The government wants 300 thousand new homes built every year,  but where should they go? Local authorities are under pressure and campaigners want to protect green spaces. How can we get the balance between the need for new homes and sustainability?Join me as I discuss these issues and more with Helen Marshall, director of the Campaign to Protect Rural England, Oxfordshire and Maxwell Marlow from the Adam Smith Institute  whose new report suggests allowing homeowners to build up to eight storeys high will alleviate the housing shortage and benefit the economy.We explore the option of building on brownfield sites, land that has previously been developed. We talk about the role of solar. We look at the new report by the Adam Smith Institute: Cooped Up, quantifying the costs of housing restrictions. Should planning regulations be eased to encourage more building, or tightened up to protect the environment? Can we have more houses and still save our green spaces for future generations? This podcast is supported by Stretto Architects an award-winning, design-led architect studio based in Bristol. Stretto has a dedicated team specialising in environmentally sensitive urban regeneration and a commitment to supporting projects rooted in social good.Contributors:CPRE - Britain's Countryside Charity Adam Smith Institute#recession #housingcrisis#UrbanPlanning#Sustainability#GreenSpaces#BrownfieldSites#SolarPower#AdamSmithInstitute#HousingShortage#CampaignToProtectRuralEngland#StrettoArchitects#EnvironmentallySensitiveDesign#UrbanRegeneration#UKHousing#Homeownership#AffordableHousing#HousingPolicy#GreenBuilding#SustainableDevelopment#EnvironmentalConservation#LandUse#HousingMarket#PolicyDebate#EconomicGrowth#ClimateAction#SustainableCities#CommunityEngagement#UrbanRenewal#GreenLiving#SmartCities#LandDevelopment#PublicPolicy#SocialGood#PlanningRegulations#NewHomes#BuildingDevelopment#EconomicImpact#CommunityDevelopment#FutureGenerationsSupport the showhttps://www.angelawalkerreports.com/

Imagine the unimaginable—losing your child to a highly poisonous gas while he's asleep in his home. This is the heart-wrenching reality that our guests, Zane Gbangbola's parents, Kye Gbangbola  and Nicole Lawler lived through. As we walk together through the series of events that led to this, we uncover a tale of environmental negligence, unaccountable authorities, and a fight for justice fuelled by Zane's parents' love. We shed light on the impact of widespread flooding in Surrey, the illegal landfill site neighbouring their home, and the tragic loss of seven-year-old Zane to hydrogen cyanide poisoning.How far would you go for the truth? That's the question Zane's parents pose as they campaign tirelessly for a public inquiry into their son's death. The Hillsborough law, a tool potentially aiding their fight, comes into our discussion as we navigate through their journey. With support from prominent politicians like Keir Starmer and Jeremy Corbyn, they're not just battling for justice for Zane, but raising awareness about secret landfill sites across the UK, hoping to prevent similar tragedies. This isn't just a conversation—it is a call to action, a wake-up call to the devastating effects of environmental hazards, and a plea for accountability. https://www.truthaboutzane.com/updates/zanes-law#TruthAboutZane#JusticeForZane#EnvironmentalJustice#CyanidePoisoningAwareness#FightForTruth#ParentalAdvocacy#HillsboroughLaw#EnvironmentalHazards#PreventTragedies#SecretLandfillSites#AccountabilityMatters#ZanesLegacy#PodcastAlert#RaiseAwareness#StopEnvironmentalNegligence#PublicInquiryNow#HydrogenCyanideAwareness#CallToAction#PodcastCommunity#ListenAndLearn#ProtectOurChildrenSupport the showhttps://www.angelawalkerreports.com/

Two years ago BBC sports reporter Chris Slegg was told the unexpected news that he needed a heart transplant within a year.  He was only 41. Married, with two children, the news plunged him into a deep depression as he feared for the wellbeing of his children.https://www.doctors.net.uk/AngelaWalkerI first worked with Chris and his wife about fifteen years at BBC London TV News. In an emotional interview, Chris shares his experience in living with the rare condition Ebstein's Anomaly. He wants to draw attention to the disease - as well as encouraging other people with life-changing diagnoses to seek psychological support. We are also joined by Mina Arvanitopoulou, a clinical psychologist specialising in cardiology. Mina supported Chris as he struggled to come to terms with his illness. Last year, Chris had pioneering surgery, which has enabled him to avoid a transplant for now.  In this podcast Chris paints a vivid picture of his journey, sharing his fear of revealing his heart-wrenching diagnosis to loved ones, the emotional rollercoaster that ensued, and the unexpected lessons he learned along the way.Mina shines a light on the importance of self-compassion, the power of vulnerability and the potential for post-traumatic growth. Join me as I talk to two inspirational guests and discuss the under-reported issue of Ebstein's Anomaly.This episode is kindly sponsored by  Doctors net uk. With over 250,000 members, Doctors net uk is the UK's largest professional network of GMC-verified doctors. They are a community that enables you to make connections, find support and improve your clinical knowledge and practice, all in one place. Join your colleagues today. https://www.doctors.net.uk/AngelaWalkerAs well as a being a sports reporter, Chris is a published author.A History of the Women's FA Cup Finalhttps://tinyurl.com/282v6hz9"The Team That Dared To Do: Tottenham 1994/95"https://tinyurl.com/53appnjchttps://www.angelawalkerreports.com/#HeartTransplant#EbsteinsAnomaly#RareCondition#HealthJourney#LifeChangingDiagnosis#MentalHealth#Vulnerability#SelfCompassion#PostTraumaticGrowth#MedicalMiracle#BBCSports#Inspiration#Cardiology#Surgery#Podcast#Healthcare#HeartHealth#MedicalBreakthrough#EmotionalJourney#SupportSystem#HealthcareHeroes#PatientStories#CardiologyCare#MedicalJourney#LifeLessons#MentalWellness#HealthAwareness#InspirationalTalk#LivingWithIllness#RareDiseaseAwareness#SharingIsCaring#MedicalSupport#BBCReporter#HeartDisease#PodcastInterview#HealthTalk#Empowerment#Wellbeing#HealthPodcast#ChronicIllnessSupport the showhttps://www.angelawalkerreports.com/

Every time untreated sewage is dumped in our rivers millions of microplastic particles also make their way into the water. When these discharges take place during low river flows, the microplastics settle on the riverbed, coated in a cocktail of chemicals and pathogens. These particles can be mistaken for food by hungry fish, thereby threatening fish populations and the wider river ecosystem.Professor Jamie Woodward from The University of Manchester has been investigating just how deep this problem runs. It was his team's research that revealed the River Tame in Greater Manchester has the highest concentration of channel bed microscopic particles ever recorded. Professor Woodward's research showed more than just the level of contamination. It revealed that the only way such high levels of microplastics could be found on the river bed was through the dumping of untreated wastewater outside of permitted conditions - that's because conventional sewage treatment is very effective at removing the microplastic particles from wastewater. Water companies dispute his findings, although he is world-renowned as a physical geographer with expertise in river catchment systems and his microplastic research has been published in Nature journals where peer review and editorial scrutiny are of the highest order. Two years after the publication of this work the water companies have not come up with a better explanation for these microplastic data.DEFRA and United Utilities were invited to join us on this podcast to discuss the issue of microplastics, but both declined. You can hear their statements.  Professor Woodward asserts that untreated wastewater must be being discharged into rivers during low flows and dry weather. This is not permitted and should only happen in "exceptional circumstances". The implications of his work on microplastics are in good agreement with other independent studies of water company behaviour that have identified dry weather spilling of wastewater as widespread.As we delve deeper into this pressing environmental crisis, we tackle the UK's consideration of a wet wipe ban and explore potential strategies to staunch the flow of microplastics at source. Professor Woodward's innovative sampling methods are put under the spotlight, and we grapple with the troubling role of microbeads from personal care products and industrial processes in contributing to microplastic pollution. We're not just here to expose the problem - join us as we champion the noble cause of cleaner rivers and consider practical solutions to this urgent issue. Tune in to this eye-opening discussion for an insight into the silent threat lurking in our waterways and how we can fight back.Support the showhttps://www.angelawalkerreports.com/

EXCLUSIVE. Government commits to reviewing new evidence in Primodos scandal for first time.Families who believe miscarriages and devastating birth defects were caused by the NHS-prescribed pregnancy test Primados say it's a fantastic positive that the British government has told this programme it is "committed to reviewing all new evidence on hormone pregnancy tests and adverse effects in pregnancy."The Government and pharmaceutical company Bayer have been accused of bullying the campaigners into silence, by threatening that, unless they commit to never making another claim, they will have to pay the legal bills of the lawyers used to block their joint action.Marie Lyons took the oral hormone pregnancy test in 1970. Her daughter was born with a badly deformed arm. But the potential risks of the damage to unborn babies had been raised by medical professionals years earlier. In our enlightening talk with Marie, an advocate from the Association for Children Damaged by Oral Hormone Pregnancy Tests, we trace the timeline of events that began with the introduction of Primados  in 1958. We hear Marie's poignant recollections of her daughter Sarah's struggles during her schooling years and in relationships due to her disability.Marie discusses the Association's High Court battle and how the Government and Bayer filled the court with teams of legal experts, dwarfing their representation.Fifty years since she started her campaign for justice, Marie remains determined to uncover new evidence to prove her case. We hear statements from the Department of Health and Social Care and Bayer who maintain their denial of any link between HPTS and foetal harm. They were invited to take part in the discussion but declined.In the final segment of our talk with Marie, we expose the devastating consequences of the drug company's decision to unlawfully distribute the drug in nations where abortion is illegal. Hear Marie's fears for her daughter's future health, the distressing tales of other association members, and the complexities of estimating the number of people affected. As we ponder the heated debate in Parliament and Theresa May's actions post-reading the expert working group's report, Marie stresses the need for an independent review of the MHRA and funding for an independent review of synthetic hormones. Her message is clear and uncompromising: the quest for justice and safety in healthcare is a fight that's far from over.https://primodos.org/#Primados#NHSprescribedpregnancytest#Hormonepregnancytests#Pregnancytestcontroversy#MarieLyons#AssociationforChildrenDamagedbyOralHormonePregnancyTests#Primadoshistory#Primadoscampaign#NHSandPrimados#Bayerpharmaceuticalcompany#Legalbattle#DepartmentofHealthandSocialCare#Foetalharm#MHRA (MedicinesandHealthcareproductsRegulatoryAgency)#Synthetichormones#Healthcaresafety#AbortionandPrimados#Expertworkinggroupreport#TheresaMay#MarieLyonsStory#PrimadosControversy#PregnancyTestScandal#HealthcareInjustice#PatientAdvocacy#MedicalNegligence#PharmaceuticalScandals#BirthDefects#LegalChallenges#HealthcareTransparency#MedicalRegulation#GovernmentAccountability#PatientRights#FoetalDevelopment#HealthcareEthics#HealthcareAdvocacy#Women'sHealth#MedicalResearch#PatientSafety#MedicalControversies#JusticeinhealthcareSupport the showhttps://www.angelawalkerreports.com/

Are you ready to unravel the complex world of Ehlers-Danlos Syndrome (EDS)? This in-depth discussion with Sarah Hamilton from Ehlers-Danlos Support UK is set to provide an enlightening perspective on this rare connective tissue disorder that affects roughly one in 500 people. From offering a closer look at the myriad of symptoms to unravelling the challenges in securing an accurate diagnosis, this comprehensive dialogue is designed to shed light on the often overlooked serious consequences of EDS.As we delve further into the societal impact of EDS, one cannot ignore the inadequate government response to the healthcare needs of those affected. The narrative of EDS going undiagnosed due to scarce resources, lack of education, and a lackluster government response is sadly all too common. Yet, as Sarah and I explore, it's not just about joint issues; many individuals experience more debilitating symptoms and are left without adequate support. Beyond the academic discourse, our conversation takes a pragmatic turn as we discuss self-management strategies and workplace accommodations for chronic illness. Sarah lends valuable insights on the importance of self-advocacy, pacing, and advocating for reasonable adjustments at work. We also examine the potential impact of initiatives like the red seeds framework, the major conditions strategy, and MSK services. If EDS affects you or someone you care about, this conversation is a treasure trove of insights, strategies and hope. Tune in, learn and lend your voice to the conversation.https://www.ehlers-danlos.org/Support the showhttps://www.angelawalkerreports.com/

Imagine receiving the life-altering news that your child has been diagnosed with a serious illness and then losing your job when you take time away to look after them.Christina Harris has lost her job of 19 years because she is looking after her daughter Skye who has been diagnosed with leukaemia. Christina courageously shares her struggles of balancing the care of her critically ill daughter with the fear of financial insecurity.Christina tells us about her petition, demanding the government makes it a parental right to take a career break for families grappling with serious childhood illnesses. Garnering over 80,000 signatures, Christina's fight has drawn significant attention but still lacks solid governmental backing.  Is it too much to ask that parents' jobs be held open for them until they can return to work? https://petition.parliament.uk/petitions/638449Support the showhttps://www.angelawalkerreports.com/

Have you ever wondered what it takes to swim the English Channel solo? Meet Laura Reineke, a fearless woman, fresh from the challenge. She shares her riveting 15-hour journey, fighting harsh weather, jellyfish and huge tankers, all while maintaining a laser-like focus and determination. Laura's monumental feat wasn't just a personal triumph, but a clarion call to address the pressing issue of water pollution. Laura tells us how her  work campaigning for clean water as one of the Henley Mermaids swimmers has taken her across the country as she stands alongside the likes of Feargal Sharkey and Steve Backshall demanding water companies are held to account. Her story is a testament to the unbeatable human spirit and the power of single-minded resolve. She's a staunch crusader against sewage pollution in the Thames and advocates for robust sewage treatment systems. She's also a believer in music for all, and founder of the charity Henley Music School, but the school is struggling financially. Without additional funds it won't be able to carry on and hundreds of people in Henley who benefit from subsidised lessons,including hundreds of children and people with additional needs will lose out . #SwimmingChallenge #EnvironmentalActivism #CleanWater #WaterPollution #ThamesRiver #SewagePollution #CharityWork #Fundraising #HenleyMusicSchool #HumanSpirit #Inspiration #Determination #SingleMindedResolve #Activism #CommunitySupport #ChannelSwim #OpenWaterSwimming #SwimmingAchievement #WaterAdvocacy #EnvironmentalAwareness #SustainableLiving #ActivistLife #CommunityEngagement #WaterQuality #HenleyMermaids #CampaignForChange #SupportLocalCharities #MusicEducation #HenleyCommunity #CleanThamesSupport the showhttps://www.angelawalkerreports.com/

More than half of mothers have experienced physical or psychological birth trauma leading them less likely to have more children because of their experience of maternity care. That's according to a study by Mumsnet instigated by Conservative MP Theo Clarke. She has founded an all-party parliamentary group on birth trauma to advocate for change following her own harrowing experience during childbirth, where she faced a third-degree tear and emergency surgery.In this episode I sit down with a courageous couple, Angelisa and Veneline Nikolov, who openly share their emotional journey through birth trauma. We also engage in a compelling discussion with Kim Thomas from the Birth Trauma Association,  and I share my own experiences of birth trauma including a complication called shoulder dystocia which left me and my newborn with serious injuries.We delve into the profound impact of childbirth trauma on women's mental health, exploring the flashbacks, physical and mental injuries, guilt, and isolation that can follow. Angelisa and Veneline's candid stories emphasize the critical need for empathy and support for those who have experienced birth trauma.We talk about the attitude of health care workers and our feeling of failure after our traumatic births -and what can be done to help people who suffer from birth trauma and how the system can be improved.Tune in as we explore these crucial issues and call for a more compassionate approach to childbirth and improved maternity care for all women.#BirthTrauma#MaternityCare#EmpathyInHealthcare#MentalHealth#SupportForMothers#ChildbirthJourney#AdvocacyForChange#BirthTraumaAwareness#CompassionateCare#MaternalMentalHealth#ParentingJourney#MotherhoodMatters#NewParents#FamilySupport#WomenEmpowerment#HealthcareAdvocacy#BirthStories#EmpoweringMothers#MaternalSupport#MaternityRights#MaternalWellbeing#HealthcareReform#MaternityExperience#SharingStories#AwarenessMattersSupport the showhttps://www.angelawalkerreports.com/

Meat reared overseas using practises that would be illegal in the UK is being sold alongside British meat  to unwitting consumers. Jacob Rees Mogg, North East Somerset Conservative MP has called for the UK to import 'hormone-injected beef' from Australia and the scrapping of import tariffs on food to open up trade. He said: "I want cheaper food. I want hormone-injected beef from Australia. I've eaten beef in Australia, it's delicious. There's nothing wrong with it."Ben Gibbons from the National Farmers Union says trade deals are threatening the UK's farming industry by opening up the market to unfair competition and poor quality imports produced to lower environmental standards.Fourth-generation farmer Anna Longthorpe says misleading food labels are undermining  British farming and she wants the government to act. They are calling for  clear, accurate, and simple labels, specifically advocating for a prominent country of origin display.ASDA, Tesco, Defra and the Competitions Authority declined to join us for our discussion.We explore the idea that consumers are more likely to buy products clearly labelled as British, shedding light on the potential impact of food security on the nation's agricultural production.   We scrutinize the government's approach to foreign  trade deals and their impact on food security, we also discuss initiatives like 'Back British Farming Day'. Finally, we delve into the challenge of ensuring that British products are accessible to all budget shoppers, emphasizing on pushing for policies that support sustainable farmers and supply chains. Tune in to gain insights into these pressing issues and more!#farm #farming #farmers #womenfarmers #britishfarming #pork #beef #meat #foreignimports #batterychickens #industrialfarming #animalwelfare  #misleadinglabelling #asda #tesco #lidl #defra #lowerwelfarestandards #buy british #bestofbritish #supermarketsmisleadingconsumers #newzealandlamb #highwelfareproduce #outsidereared #unfaircompetition #tradedeals #brexit #FoodTransparency #ConsumerRights #FarmToTable #EthicalFarming #LocalProduce #QualityControl #Sustainability #EnvironmentalImpact #BuyBritish #TradePolicy #EconomicImpact #SupportFarmers #FairMarket #ImportRegulations #FoodPolicy #FoodSecurity #BritishFarming #FoodLabels #TradeDeals #Agriculture #FoodSafety #SustainableFarming #ConsumerAwareness #BackBritishFarming #EnvironmentalStandards #FarmersUnion #UKAgriculture #FairTrade #SupplyChain #FoodQualitySupport the showhttps://www.angelawalkerreports.com/

Why do we never talk about involuntary male childlessness? A quarter of men do not have children and for many of them this is not through choice.   Join me as I sit down with my guest, Dr. Robin Hadley, academic and author of 'How is a Man Supposed to be a Man?'. We explore male childlessness,  the stereotypes that often stifle men's discussions about their yearning for parenthood and their struggles with fertility. With Dr. Hadley's expert insight, we navigate the emotional labyrinth faced by these men and tackle the societal norms that equate virility with fatherhood.As our conversation unfolds, we turn the spotlight on the evolving perceptions of fatherhood. We delve into the pressures men face when considering paternity leave and the repercussions of the gig economy on their decision. We take a closer look at grandparenthood and its function as a social bridge for children in the absence of their parents. Moreover, we bring into focus the harsh reality of older adults without a support network or children to care for them and the uphill battle they face in society.Finally, we discuss - the profound psychological impact of male infertility. We rip apart societal misconceptions that exacerbate the stigmas around male childlessness and infertility. Dr. Hadley emphasizes the critical need for therapy and the establishment of safe spaces for men to express their vulnerability. So, tune in as we break barriers, challenge conventional wisdom, and underscore the significance of understanding and empathising with the emotional challenges encountered by childless men.#MaleChildlessnes #Infertility #ParenthoodStruggles #DrRobinHadley #FatherhoodPerceptions #EmotionalChallenges #MensHealth #Stereotypes #SupportNetworks #TherapyForMen #InvoluntaryChildlessness #FertilityJourney #PaternityLeave #GigEconomyImpact #Grandparenthood #SupportingChildlessMen #SocialNorms #MentalHealthMatters #BreakingStigmas #SafeSpacesForMen #UnderstandingEmotions #ChallengingSocietalExpectations #MaleInfertility #EmpathyMatters #MenTalkParenthood #bbc #bbcnews #gmb #skynews  #worldchildlessweek #babiesRegenerateSupport the showhttps://www.angelawalkerreports.com/

Imagine what it's like not to be able to eat, not because of a lack of food, but because of a rare disorder that prevents your body from processing it. This is the reality for our guest, Celia Chartres-Aris, living with Loeys-Dietz Syndrome. Celia's condition requires her to be reliant on a feeding tube for nutrition. Her life is a testament to resilience and strength, and she joins us to shed light on her experience, from dealing with verbal abuse to answering inappropriate questions, all while living with a feeding tube. Our conversation takes a critical turn as we scrutinize how legislation often fails to protect those with disabilities. With Celia's life as a backdrop, we examine poignant examples like the introduction of the Down Syndrome Bill, the care for children, and current access and architecture requirements for public buildings. We focus on the urgent need for inclusive policy making that involves the disabled in the process, underscoring the importance of designing everything right from the outset, with accessibility in mind. The final part of our discussion turns to the crucial aspect of accessibility and inclusion. Listen as Celia recounts instances where she was denied access due to her disability, and how she uses these moments to educate others. We explore the Access Maturity Model, a tool organizations can use to assess their inclusion and accessibility policies. We conclude our conversation by emphasizing the importance of diversity inclusion, stressing the need for disabled people to be included in design and entrepreneurship roles, and a deep understanding of these critical issues.#DisabilityRights #Inclusivity #Accessibility#InclusiveDesign #DisabilityAdvocate #Access2Funding#Legislation #PublicBuildings #Resilience#DisabledEntrepreneurs #CeliaChartresAris#FeedingTubeLife #DiversityandInclusion #GovernmentAdvisory#DisabilityAwareness #AccessibleSpaces #InclusivePolicy #ForbesFeature #DiscriminationAwareness #AccessDeniedSupport the showhttps://www.angelawalkerreports.com/

What if you could better understand the complex world of dementia and discover ways to connect with your loved ones affected by it? In today's episode we meet  Shirley Pearce, the CEO and founder of Understanding Dementia. A retired occupational therapist, Shirley's compassion, personal commitment and years of experience have led to the creation of a unique programme that reshapes traditional care approaches by focusing on enhancing the emotional wellbeing of dementia patients.We discuss the nature of dementia, its devastating effects and the tools offered by Shirley's programme to help for caregivers develop new skills. Shirley's valuable insights extend to real-life scenarios, like managing communication hurdles or finding strange items in the fridge, emphasising the importance of understanding human behaviour when caring for dementia patients. We also delve into her ABC programme, which is designed to minimise frustration and confusion  for people with dementia and their families.This episode is a journey through the often misunderstood landscape of dementia care, filled with hope, compassion, and practical guidance. Whether you're a family member, healthcare professional, or someone dealing with dementia, you're bound to find this conversation both enlightening and empowering. Join us as we shed light on the complex world of dementia and explore how hope can be found after a diagnosis.angelawalkerreports.comhttps://understandingdementia.co.uk/#DementiaCare #UnderstandingDementia #EmotionalWellBeing #CaregivingSkills #dementia  #elderly  #elderlypatients #ABCTransition #QualityOfLife #EmpowermentAfterDiagnosis #InnovativeCaregiving #NavigatingChallenges #CompassionateCare #EnlighteningInsights #HopeForDementia #nhs #dementiaawarenessSupport the showhttps://www.angelawalkerreports.com/

Water companies in the UK have been dumping ever-increasing amounts of sewage into our rivers and waterways. Now, a law suit could hit them where it hurts and cost them hundreds of millions of pounds. Law firm Leigh Day is leading a collective action accusing them of abusing their dominant position by over-charging customers. The action hinges on the allegation that water companies knowingly failed to report the number and extent of sewage discharges and were therefore  allowed to charge customers more.  The first claim has been issued against Severn Trent and further claims will be issued against Thames Water, United Utilities, Anglian Water, Yorkshire Water and Northumbrian Water. Zöe Mernick-Levene , a partner at law firm Leigh Day explains the case against them which is being brought by Professor Carolyn Roberts an environmental and water consultant.Ashley Smith from campaign group Windrush Against Sewage Pollution joins us to talk about his work and explain how mathematician Peter Hammond used AI to expose thousands of unnoticed spills. We delve into how this data is captured, scrutinized and the  fact that just 1% of it is reviewed by the environment agency. We'll probe into why water companies are being secretive about data and the crucial impact of citizen scientists in pushing the case forward. We'll also be discussing the reports from dozens of elite triathletes who say they fell ill after competing in the World Championships in Sunderland's water and the response from Northumbria Water. Listen in as we scrutinise the statement issued by the Environment Agency and DEFRA .Brace yourself for a deep dive into the legal challenges faced by water companies for their pollution. Ashley unfolds the inception of Windrush Against Sewage Pollution and its efforts to expose the deteriorating condition of the River Windrush.  Zöe uncovers their legal warfare using opt-out claims to make corporate giants rethink their actions. We'll also compare the water systems globally to the UK's, exploring how privatisation led to profits at the expense of infrastructure. Ending on a note of damages, we decipher how a tribunal would decide the overpayment for each customer.#WaterPollutionUK #SewageScandal #EnvironmentalJustice #WaterwayAbuse #LegalAction #CorporateAccountability #PollutionLawsuit #SewageDischarge #RiversInDanger #EnvironmentalImpact #CitizenScientists #AIExposesPollution #CleanWaterRights #CorporateMisconduct #TransparencyMatters #RiverHealth #WaterwayProtection #PrivatizationEffects #GlobalWaterSystems #PollutionConsequences #LegalChallenges #InfrastructureImpact #CorporateResponsibility #SustainabilityMatters #PollutionAwareness #EnvironmentalAdvocacySupport the showhttps://www.angelawalkerreports.com/

Hundreds of deaths from epilepsy could be prevented every year if the condition was managed properly - according to the founder of a British charity.In the UK, at least 1,000 people with epilepsy die each year.  In this powerful and informative podcast, journalist Angela Walker sits down with Jane Hanna OBE from SUDEP Action, who says many of these deaths could be prevented if changes were made in by the NHS,  in local healthcare management and if care for the the condition was properly funded  by the government.Having lost her partner to sudden death in 1990, Jane is passionate about preventing such tragedies and shedding light on the often under-reported issue of sudden unexpected death in epilepsy .Jane shares her personal experience and reveals that every week, around 21 families face the same devastating loss. SUDEP occurs when an individual diagnosed with epilepsy or experiencing seizure-related episodes suddenly passes away, usually during sleep, with no prior warning signs. Angela and Jane delve deeper into the risk factors associated with SUDEP and discuss the importance of raising awareness among medical professionals and the public.The discussion also explores the challenges faced by the medical community in managing epilepsy cases and calls for a change in protocols to prioritise early diagnosis and intervention. Jane explains about the SUDEP app which can help patients and medics manage the condition better.The podcast delves into the alarming rise in maternal deaths related to epilepsy and discusses the potential link with certain antiseizure medications. Jane highlights the importance of specialized communication and counselling for pregnant women with epilepsy,.Join Angela Walker and Jane Hanna as they bring this critical issue to the forefront, sharing inspiring stories and insights from individuals and families impacted by epilepsy. Through awareness, understanding, and collaborative efforts, they believe that many of these heart-wrenching deaths can be prevented, paving the way for a safer future for those living with epilepsy.#EpilepsyAwareness #SUDEPAction #PreventEpilepsyDeaths #HealthcareChange #EpilepsyManagement #RaisingAwareness #EpilepsyPodcast #MedicalCommunity #EarlyDiagnosis #SUDEPApp #MaternalHealth #PregnancyAndEpilepsy #CollaborativeEfforts #SaferFutureSupport the showhttps://www.angelawalkerreports.com/

Imagine having unlicensed toxins injected into your face by someone with no training. That's what is happening across the UK every day - with disastrous  results. Nurse Practitioner Sarah Healey and Ashton Collins from campaign group Save Face join me to discuss the alarming lack of regulation in the booming non-surgical aesthetics industry. Hear how unscrupulous beauticians are buying unlicensed products from overseas and injecting unwitting consumers with saline, beef gelatine and other products.Sarah, who's been shortlisted for a Safety In Beauty Award, gives us a first-hand account of the process she follows when dealing with patients seeking injectable treatments and the risks they pose. We also discuss how social media and reality TV have played their role in escalating the demand amongst the young, and why it's more important than ever to ensure you're in the hands of a suitably trained and certified practitioner. So, tune in, as we end with a discussion around the current standards in aesthetic treatments and how to ensure your safety in this rapidly growing industry.In loving memory of my friend Sarah, who died suddenly on 6th November 2023, and who always  believed in doing the right thing.Support the showhttps://www.angelawalkerreports.com/

Why are so many childcare providers in the UK feeling the financial strain, and are the government's budget promises enough to tackle the issue? Listen in as we chat with Ian Morgan from the campaign group Champagne Nurseries for Lemonade Funding and director of Little Ducklings Nursery in Berkshire.  We delve into the challenges that the UK childcare industry is facing due to inadequate funding. We explore the increasing cost of staffing, the struggle to retain staff, and the impact of soaring costs for energy and food on providers.Ian shares his 16 years of experience in the industry and his hopes for its future, as well as the challenges faced by childcare providers . We also discuss the feelings amongst people in his group, Champagne Nurseries, Lemonade Funding, and potential solutions for providing quality childcare at an affordable cost for parents. Tune in to find out if the government's recent efforts will be enough to ease the burden on childcare providers and if the industry can adapt and thrive amidst these challenges.Support the showhttps://www.angelawalkerreports.com/

What if you could overcome the limitations of a rare disability and achieve extraordinary feats? Join us for an inspiring conversation with Isaac Harvey MBE, who has done just that. Born with limbpelvic hypoplasia, Isaac has adapted to life without arms and short legs, using his feet as hands.In this episode, we explore his personal story, including the challenges he faced, his adventurous side, and his incredible achievements.We discuss Isaac's experiences growing up in Ilford, navigating public transport, and becoming involved with 'Wheels and Wheelchairs,' a group running in the streets of London. Hear how he conquered high-octane sports like abseiling, skiing, and sailing  pushing himself to achieve his goals and inspiring others. And we'll find out about his recent MBE award, his upcoming events, and his new venture into media production with his company Seated Perspective.Finally, we delve into the power of motivation and self-belief, exploring how Isaac's determination and passion have helped him overcome setbacks and achieve the seemingly impossible. Discover the key to turning obstacles into opportunities and finding inner peace through struggles. Don't miss this uplifting episode that will leave you feeling inspired and motivated to face your own challenges head-on.Support the showhttps://www.angelawalkerreports.com/

3.8 million people in the UK experienced destitution in 2022, including around one million children. That's according to the Joseph Rowntree Foundation report into destitution. This is almost two-and-a-half times the number of people in 2017, and nearly triple the number of children. There is an urgent need for action to tackle destitution in the UK.When faced with the reality of not being able to provide basic essentials for your child, where do you turn for help? In our heartfelt conversation with Emma Cantrell, founder and CEO of Children's Charity First Days, we uncover the shocking statistics surrounding child poverty and food insecurity in the UK. Emma shares the touching story of how First Days began and its growth over the past decade, now supporting over 10,000 children living in poverty by distributing more than 250 tonnes of donated goods.We discuss the vital role of providing children with brand new items on their first day of school, granting them a sense of agency and belonging. Emma sheds light on the challenges of supplying school uniforms amidst rising costs and the disturbing fact that 20% of adults in the UK have experienced food insecurity. We delve into the impact of this crisis on families and their children's well-being and future prospects.In this episode, Emma also shares her insights on how First Days Charity not only meets the basic needs of impoverished families but builds relationships with them to ensure they receive the help they deserve. We explore the inspiring ways the local community comes together to support those in need, as well as the importance of breaking down the stigma around asking for help. Join us for this inspiring and eye-opening conversation with Emma Cantrell, a true champion for children in need.#ChildPovertyUK #FoodInsecurity #ChildrensCharity #FirstDays #HelpingChildren #CommunitySupport #ChildWellbeing #EducationMatters #BasicNeeds #SupportingFamilies #BuildingConnections #InspiringChange #ChildhoodPoverty #GivingBack #CommunitySolidarity #BreakTheStigma #EmpowerChildren #MakingADifference #ChildAdvocacy #UKCharities #ChildhoodInequality #FutureProspects #SocialImpact #PovertyAwarenessSupport the showhttps://www.angelawalkerreports.com/

Thousands of people were infected with HIV and Hepatitis after being given contaminated blood by the NHS in the 1970s and 80s. Many have since died - more are gravely ill.  The government has been directed to pay compensation to those affected and quickly, yet hundreds of people haven't received a penny. Jason Evans lost his father when he was four years old as a result of the infected blood scandal. He spearheaded a mission for truth and justice by setting up campaign group Factor 8 to demand a public inquiry and now he's fighting for the compensation agreed to be paid out.  Joined with Des Collins, a formidable solicitor advocating for hundreds of victims, we delve into this shocking chapter of medical history and its ongoing implications. Hear their stories, the relentless hunt for damning documents, and the profound determination of victims fighting for their rights.Des Collins and Jason Evans share invaluable insights about the bureaucratic red tape that has delayed compensation and justice for those affected. We dive into the intricacies of the Robert Francis report from 2022, the Langstaff report's recommendations, and what these delays mean for those still awaiting compensation.Through their tales of persistence and resilience, Jason and Des will bring us face to face with the realities of trying to hold government officials accountable. #HIVHepatitisScandal #InfectedBloodControversy #NHSCompensation #Factor8Campaign #PublicInquiryDemand #MedicalHistory #CompensationDelays #RobertFrancisReport #LangstaffReport #GovernmentAccountability #VictimsRights #BureaucraticRedTape #JusticeForAll #MedicalInjustice #HealthcareScandal #VictimAdvocacy #TruthAndJustice #CompensationStruggle #GovernmentResponsibilitySupport the showhttps://www.angelawalkerreports.com/

Get ready to be captivated by the miraculous story of Bharti Dhir, a woman abandoned as a newborn baby in Uganda, who overcame unimaginable hardships in her life. We sit down with Bharti as she shares the life-changing moment when she was discovered and adopted by a local Punjabi Sikh family, and how her mother's prophetic dreams of a baby girl played a role in this incredible tale.Bharti's journey was far from easy, as she faced many challenges growing up with a dual heritage and a rare skin condition called Epidermolysis Bullosa (EB). In our conversation, Bharti reveals the various unconventional treatments her father sought to cure her condition, and how her family's unwavering love and support led her towards self-acceptance and healing. Hear the emotional details of her childhood battle with EB and her path to embracing her unique identity.Bharti  recounts the harrowing experiences she and her family faced while living under the brutal regime of Idi Amin in Uganda. Through tales of danger, escape, and the strength of her family's love, Barty's incredible resilience and positivity will leave you in awe. Don't miss this powerful episode, and be sure to pick up Barty's memoir, 'Worth', to learn even more about her remarkable life story.bhartidhir.comSupport the showhttps://www.angelawalkerreports.com/

Are you an entrepreneur seeking guidance on securing investment and navigating the start-up landscape? Join us for an insightful discussion with award-winning entrepreneur, Leroy Lawrence, and Matt Adey, the Director of Economics for British Business Bank. Discover the unique challenges facing start-ups in the UK, especially in the current economic climate, and learn how British Business Bank is helping smaller businesses get the finance they need to start, grow, and develop.Leroy shares his experience of taking his innovative business idea, Pigee Post, to Asia to secure investment, as he felt constrained by the mindset of British investors. We delve into why British investors might be hesitant to take enough of a risk and invest a large enough amount, compared to their American counterparts. Matt also sheds light on the efforts of British Business Bank in supporting angel investors and early-stage venture capital funds.Don't miss out on valuable insights and advice for aspiring entrepreneurs as we discuss the importance of finding the right investor who understands your vision and goals, and explore the different types of finance available to start-ups. Whether you're an entrepreneur looking to make your mark or simply seeking inspiration, this episode is not to be missed.Support the showhttps://www.angelawalkerreports.com/

Why are victims of the infected blood scandal still waiting for compensation despite a directive from the Infected Blood Inquiry chair? Meet the extraordinary man who says his disability is his strength. Plus the nurse practitioner who says the UK is the "Wild West" of the non-surgical beauty aesthetics world. My guests Jason Evans, Isaac Harvey and Sarah Healy.Trailer. Follow and subscribe.#InfectedBloodScandal #contaminatedblood #CompensationDelay#InfectedBloodInquiry #botchedbotox #DisabilityStrength #NonSurgicalBeauty#UKWildWest #Aesthetics #factor8 #JasonEvans#IsaacHarvey #SarahHealy #PodcastDiscussion#MedicalJustice #journalism #angelawalkerreports#SocialJustice #InquiryUpdates #CompensationRightsSupport the showhttps://www.angelawalkerreports.com/

Thousands of people were infected with HIV and Hepatitis after being given contaminated blood by the NHS in the 1970s and 80s. Many have since died - more are gravely ill.  The government has been directed to pay compensation to those affected and quickly, yet hundreds of people haven't received a penny. Jason Evans lost his father when he was four years old as a result of the infected blood scandal. He spearheaded a mission for truth and justice by setting up campaign group Factor 8 to demand a public inquiry and now he's fighting for the compensation agreed to be paid out. The full interview will launch on 3rd July. Subscribe now.#HIVHepatitisScandal #InfectedBloodControversy #NHSCompensation #Factor8Campaign #PublicInquiryDemand #MedicalHistory #CompensationDelays #RobertFrancisReport #LangstaffReport #GovernmentAccountability #VictimsRights #BureaucraticRedTape #JusticeForAll #MedicalInjustice #HealthcareScandal #VictimAdvocacy #TruthAndJustice #CompensationStruggle #GovernmentResponsibilitySupport the showhttps://www.angelawalkerreports.com/

Join former BBC reporter and broadcast journalist Angela Walker as she engages in thought-provoking conversations with inspirational individuals about current affairs and under-reported issues. In this podcast, we aim to shed light on important topics that often go unnoticed, providing a platform for insightful discussions.From activists and social entrepreneurs to academics and community leaders, these individuals bring their expertise and experiences to the table. Through their stories, we explore the challenges they have overcome, their motivations, and the lessons they have learned along the way.Listen to be inspired and informed.Support the showhttps://www.angelawalkerreports.com/