Podcast appearances and mentions of Kate Wilson

In the season finale of Demystifying Genetics, host Matt is joined by fellow genetic counselor and podcaster, Kate Wilson, the voice behind All Access DNA. They delve into the evolving landscape of genetic counseling, exploring Kate's personal journey from rural beginnings to becoming a passionate advocate for equitable access to clinical genetics. This episode highlights the disparities within healthcare systems, the importance of accessible genetic information, and how Kate is breaking norms with her dual role as a counselor and a science communicator. Tune in for a compelling discussion on the responsibilities and opportunities for genetic counselors beyond traditional clinical roles. Enjoy this insightful conversation as Matt concludes the season and hints at exciting changes for the show's future format. Here is a link to the article (Tschirgi et al., 2023) that we discuss in this episode. This is Kate's podcast: https://allaccessdna.podbean.com/ Thank you to my sponsor TrakGene.

In this episode we are exploring two publications related to cancer care. In our first segment we talk to 2 authors about their research on genetic counselors and identification of patients for high-risk pancreatic cancer screening. In our second segment, Khalida interviews a genetic counselor about their study to evaluate surgical patient perspectives of genetic testing provided by a non-genetics professional.  Segment 1: “Practices and perspectives of genetic counselors about high-risk pancreatic cancer screening: A cross-sectional survey study” Amy Wiegand is a board-certified genetic counselor who specializes in cancer genetics. She graduated with her Master's in Genetic Counseling in 2017 from from the Icahn School of Medicine at Mount Sinai and has worked as a cancer genetic counselor at the Smilow Cancer Genetics and Prevention Program at Yale-New Haven Health since 2017 where she has seen over 2500 patients for a variety of hereditary cancer indications. Her research interests include hereditary pancreatic cancer and alternative delivery care models for genetic testing. Aparna is a senior genetic counseling assistant (GCA) at Smilow Cancer Genetics and Prevention Program at Yale New Haven Health where she has worked since 2019, and she has over 6 years of experience as a GCA. She holds a Master's degree in Biomedical Genetics and a Bachelor's degree in Biotechnology. She also has a varied background in administration, finance and customer service. She is a high-performing individual and was recently recognized by her colleagues as ‘Employee of the Quarter' and honored by the organization as ‘Smilow Star' for consistently going above and beyond for the patients and the co-workers and for exemplifying the health system's values. She contributes to the program in a variety of other ways outside of her role and works collaboratively with the team to create a patient centered environment. She has a strong interest in Cancer Genetics and is passionate about research. She is currently working on another research project, the abstract of which was selected for presentation in a Poster Session at 2025 ASCO (American Society of Clinical Oncology) annual meeting. She enjoys being part of a collaborative and dynamic team at Smilow Cancer Genetics and Prevention program and is excited about the upcoming research initiatives in the program. In this segment we discuss: - The significance of pancreatic cancer surveillance for high-risk individuals and why early detection plays a critical role in improving outcomes. - How genetic counselors are uniquely positioned to identify and refer individuals at high risk for pancreatic cancer, emphasizing their role in screening efforts. - An overview of the 2019 CAPS (Cancer of the Pancreas Screening) consensus guidelines and how they are applied to identify high-risk individuals for surveillance - The finding that nearly 70% of genetic counselors accurately identified individuals eligible for screening and discussed the factors that may have contributed to this high rate. - The association between provider comfort level and accuracy in identifying high-risk individuals, and discussed strategies to improve provider confidence and access to screening programs.   Segment 2: “Patient experiences of cancer genetic testing by non-genetics providers in the surgical setting” Katie Fiallos is a board-certified genetic counselor who earned her Master of Science in Genetic Counseling from the Johns Hopkins University/National Human Genome Research Institute Genetic Counseling Training program in 2017 and worked for seven years as a cancer genetic counselor at Johns Hopkins. She joined the Department of Medical and Molecular Genetics at Indiana University in August 2024. She is fluent in Spanish and provides genetic counseling in English and Spanish to participants with Parkinson's disease enrolled in the PD GENEration study. She has authored several academic papers related to genetic counseling, and her current research interests include provision of genetic counseling to Latine individuals, alternate service delivery models, and patient experiences with genetic testing and their informational desires. She lives in Michigan with her family and enjoys staying active, particularly practicing aerial silks. The research for the paper we're discussing was done while she was at Johns Hopkins and was funded by the Jennifer L. Brager Memorial Research award through the Johns Hopkins Kimmel Cancer Center.   In this segment we discuss: - Why hereditary cancer genetic testing is becoming increasingly important for patients with breast cancer, especially in relation to surgical decision-making. - The findings that patients preferred genetic testing at an existing appointment shortly after diagnosis, and explored how this timing affects their overall experience. - How many patients had already considered or wanted genetic testing before it was offered, shedding light on patient awareness and readiness. - Why patients were primarily motivated by concern for relatives and a desire for complete information, rather than surgical decision-making. - Gaps in patient-provider communication identified in the study and suggested ways for providers to address these issues in clinical practice.   Would you like to nominate a JoGC article to be featured in the show? If so, please fill out this nomination submission form here. Multiple entries are encouraged including articles where you, your colleagues, or your friends are authors.   Stay tuned for the next new episode of DNA Dialogues! In the meantime, listen to all our episodes Apple Podcasts, Spotify, streaming on the website, or any other podcast player by searching, “DNA Dialogues”.    For more information about this episode visit dnadialogues.podbean.com, where you can also stream all episodes of the show. Check out the Journal of Genetic Counseling here for articles featured in this episode and others.    Any questions, episode ideas, guest pitches, or comments can be sent into DNADialoguesPodcast@gmail.com.  DNA Dialogues' team includes Jehannine Austin, Naomi Wagner, Khalida Liaquat, Kate Wilson and DNA Today's Kira Dineen. Our logo was designed by Ashlyn Enokian. Our current intern is Sydney Arlen.

In this episode we feature 2 articles that explore hot topics in genetics as well as opportunities to improve patient care in honor of DNA Day on April 25. DNA day commemorates the completion of the Human Genome Project and the discovery of DNA's double helix. Both of these studies utilize qualitative methodologies to highlight people's experiences and share their stories. Segment 1: Not Parent Expected” results through direct-to-consumer genetic testing Julia Becker (she/her) is a board-certified genetic counselor and CSU Stanislaus Genetic Counseling Program graduate. She has a strong interest in the ethical, psychological, and social implications of genetic testing, particularly in the context of unexpected parentage discoveries. Julia is the first author of the article, "Experiences of Individuals Receiving ‘Not Parent Expected' Results Through Direct-to-Consumer Genetic Testing," published in the Journal of Genetic Counseling. She presented this research at the American College of Medical Genetics and Genomics (ACMG) Annual Conference in 2021, contributing to the ongoing dialogue on the impact of unexpected genetic findings. Her work focuses on supporting individuals navigating complex genetic discoveries and advancing awareness within the genetic counseling community. In this segment we discuss: - The rise in Not Parent Expected (NPE) discoveries through direct-to-consumer genetic testing and what it means to receive this result. - Key emotional themes from interviews with 25 participants, including identity disruption, grief without death, and shifting family dynamics. - How a background in genetic counseling informed a sensitive and in-depth interview approach. - The emotional motivations behind seeking out biological relatives and the varied outcomes of those efforts. - The need for improved informed consent and follow-up care from DTC companies.   Segment 2: Transgender and gender diverse patients' experiences with pregnancy-related genetics discussions: A qualitative study Jaime Schechner (she/her) works as a neurology genetic counselor at Boston Children's Hospital. She completed her Master of Science in Genetic Counseling at Boston University, and previously worked as a genetic counseling assistant at Beth Israel's Maternal Fetal Medicine Center. Darius  Haghighat (he/him) is a reproductive genetic counselor at Boston Medical Center and an Assistant Professor of Obstetrics and Gynecology at Boston University Chobanian & Avedisian School of Medicine. He has prior experience as a cancer genetic counselor as well. He completed his Master's in Genetic Counseling at Boston University. As a queer genetic counselor he is especially passionate about LGBTQIA+ health equity. In this segment we discuss: - The inspiration behind focusing the study on pregnancy-related genetic counseling experiences among trans and gender diverse (TGD) individuals. - Major gaps in reproductive healthcare for TGD patients, including misgendering, binary language, and lack of provider knowledge. - Participant stories about feeling unseen or misgendered, and discussed the emotional impact of these encounters. - Frustrations with terms like "maternal" and "advanced maternal age," and suggested inclusive alternatives for clinical language. - Moments of affirming care, showing how small gestures can have a powerful impact across the healthcare journey. - The need for systemic change, including inclusive policies, provider education, and future research that centers TGD voices. Would you like to nominate a JoGC article to be featured in the show? If so, please fill out this nomination submission form here. Multiple entries are encouraged including articles where you, your colleagues, or your friends are authors. Stay tuned for the next new episode of DNA Dialogues! In the meantime, listen to all our episodes Apple Podcasts, Spotify, streaming on the website, or any other podcast player by searching, “DNA Dialogues”.  For more information about this episode visit dnadialogues.podbean.com, where you can also stream all episodes of the show. Check out the Journal of Genetic Counseling here for articles featured in this episode and others.  Any questions, episode ideas, guest pitches, or comments can be sent into DNADialoguesPodcast@gmail.com.  DNA Dialogues' team includes Jehannine Austin, Naomi Wagner, Khalida Liaquat, Kate Wilson and DNA Today's Kira Dineen. Our logo was designed by Ashlyn Enokian. Our current intern is Sydney Arlen.

In this episode, we are discussing 2 articles focused on cardiovascular genetics. In the first segment, Khalida talks to authors Marianne and Erin about their research exploring the opportunities for downstream revenue of cardiac genetic counseling services in a pediatric medical center. In the second segment, Naomi chats with Jodie and Erin about the recent NSGC Practice Resource about genetic testing and counseling for hypertrophic cardiomyopathy. Segment 1: Cardiac genetic counseling services: Exploring downstream revenue in a pediatric medical center Marianne Olson, MS, CGC is a genetic counselor at Baptist Health in Kentucky. She provides prenatal genetic counseling at Maternal Fetal Medicine clinics in Louisville and Lexington. Marianne graduated from the Cincinnati Genetic Counseling Graduate Program in 2024. Prior to working as a genetic counselor, Marianne taught high school chemistry and biology for 12 years. Erin Miller is an Associate Professor in the University of Cincinnati College of Medicine. Erin is a genetic counselor IN THE DIVISION OF CARDIOLOGY at Cincinnati Children's Hospital Medical Center. She leads the cardiology genetic counseling team in providing genetic counseling services to individuals of all ages with and at risk for cardiovascular disease. Erin is focused on improving access to genetics services for families with inherited cardiovascular diseases. In this segment we discuss: - What sparked the decision to explore downstream revenue (DSR) in a cardiac genetic counseling setting - Financial challenges institutions face when hiring genetic counselors, especially around reimbursement - The role of genetic counseling in reducing costs by guiding risk stratification and avoiding unnecessary testing - Limited uptake of cardiac screening among at-risk relative and strategies that could help improve adherence - How findings from this study can support the case for sustaining genetic counseling roles within pediatric cardiology - Potential to adapt the study's methodology to other specialties like neurology or prenatal genetics, and considerations for doing so   Segment 2: Genetic testing and counseling for hypertrophic cardiomyopathy: An evidence-based practice resource of the National Society of Genetic Counselors Erin Miller (she/her) is an Associate Professor in the College of Medicine at the University of Cincinnati and a cardiac genetic counselor at Cincinnati Children's Hospital Medical Center in the Division of Cardiology. She leads the cardiology genetic counseling team in providing genetic counseling services to individuals of all ages with and at risk for cardiovascular disease. Erin is focused on improving access to genetics services for families with inherited cardiovascular diseases. Associate Professor Jodie Ingles (she/her)  is Head of the Clinical Genomics Laboratory and Program Director of Genomics and Inherited Disease Program at Garvan Institute of Medical Research. She is a cardiac genetic counsellor in the Department of Cardiology, Royal Prince Alfred Hospital Sydney. Her team is focused on using genomics to improve diagnosis and care of families with inherited cardiovascular diseases. In this segment we discuss: - The motivation behind creating an official practice resource focused on genetic testing and counseling for HCM - Deep dive into the first major recommendation: offering genetic testing to all individuals with a suspected or confirmed diagnosis of HCM, paired with appropriate genetic counseling - Exploration of the second recommendation: ensuring that genetic tests are selected, ordered, and interpreted within the context of genetic counseling, and the complexities that come with this process - Discussion of the third recommendation: providing cardiac and cascade genetic testing to at-risk relatives, without age limitations, and why this is critical for effective family-based care - A look at the barriers to integrating genetic services into cardiology practices, especially in settings without dedicated genetics expertise   Would you like to nominate a JoGC article to be featured in the show? If so, please fill out this nomination submission form here. Multiple entries are encouraged including articles where you, your colleagues, or your friends are authors. Stay tuned for the next new episode of DNA Dialogues! In the meantime, listen to all our episodes Apple Podcasts, Spotify, streaming on the website, or any other podcast player by searching, “DNA Dialogues”.  For more information about this episode visit dnadialogues.podbean.com, where you can also stream all episodes of the show. Check out the Journal of Genetic Counseling here for articles featured in this episode and others.  Any questions, episode ideas, guest pitches, or comments can be sent into DNADialoguesPodcast@gmail.com.  DNA Dialogues' team includes Jehannine Austin, Naomi Wagner, Khalida Liaquat, Kate Wilson and DNA Today's Kira Dineen. Our logo was designed by Ashlyn Enokian. Our current intern is Sydney Arlen.  

In this episode we are exploring rare and ultra-rare disease in honor of Rare Disease Day on February 28 which raises awareness for the 300 million people worldwide living with a rare disease. We are talking with one author about their study on the role of digital tools in rare disease management and another author about their research into experiences of parents who have a child with an emerging-ultrarare disorder. Segment 1: Exploring the role of digital tools in rare disease management: An interview-based study Andrea Chang works as a Genomic Science Liaison at Quest Diagnostics and earned her MS in Genetic Counseling from UCLA's inaugural genetic counseling class. In this segment we discuss: The role of digital tools in healthcare management for rare diseases Real-world examples of existing digital tools for the rare disease community The impact of rare disease on the global population The healthcare gaps currently not addressed by digital tools Recommended digital tool features Segment 2: The book is just being written: The enduring journey of parents of children with emerging- ultrarare disorders Bethany Stafford-Smith works clinically as a genetic counsellor at University Hospitals of Leicester. She also works for Great Ormond Street Hospital as a Research Genetic Counsellor. In this segment we discuss: The definition of emerging ultra rare disorders or E-URD Experiences of parents with children diagnosed with an E-URD Parents' perceptions on the utility of a diagnosis Challenges faced by parents seeking medical and social support after receiving an E-URD diagnosis for their child How researchers and healthcare providers can support advocacy in E-URDs Would you like to nominate a JoGC article to be featured in the show? If so, please fill out this nomination submission form here. Multiple entries are encouraged including articles where you, your colleagues, or your friends are authors. Stay tuned for the next new episode of DNA Dialogues! In the meantime, listen to all our episodes Apple Podcasts, Spotify, streaming on the website, or any other podcast player by searching, “DNA Dialogues”.  For more information about this episode visit dnadialogues.podbean.com, where you can also stream all episodes of the show. Check out the Journal of Genetic Counseling here for articles featured in this episode and others.  Any questions, episode ideas, guest pitches, or comments can be sent into DNADialoguesPodcast@gmail.com.  DNA Dialogues' team includes Jehannine Austin, Naomi Wagner, Khalida Liaquat, Kate Wilson and DNA Today's Kira Dineen. Our logo was designed by Ashlyn Enokian. Our current intern is Sydney Arlen.

On This Episode We Discuss: In this episode we explore genetic testing in low risk populations, both in direct-to-consumer and clinical settings. We interview authors on two recent JoGC papers related to topics of communication of health risks, understanding of genetic testing, and informed decision-making. You can find the Journal of Genetic Counseling webpage via onlinelibrary.wiley.com or via the National Society of Genetic Counselors website.   Segment 1: An analysis of direct-to-consumer genetic testing portals and their communication of health risk and test limitations Nicole Lee is an associate professor of communication in the School of Social and Behavioral Sciences at Arizona State University. Her research examines the intersection of science communication, public relations, and digital media. This work has been applied to many contexts including climate change, biodiversity research, wellness products, and direct-to-consumer genetic testing. x: @lee_nicole linkedin: https://www.linkedin.com/in/nicoleleepr/   In this segment we discuss: - What motivated the exploration of how direct-to-consumer (DTC) genetic testing companies communicate health risks to consumers. - Potential impacts on consumers who may misinterpret relative risk when presented without adequate context. - Importance of genetic counselors in improving interpretation and communication of DTC genetic test results. - Suggestions for enhancing transparency and clarity in communicating health risks to consumers.   Segment 2: Non-Invasive Prenatal Screening: Testing Motivations and Decision Making in the Low-Risk Population Meagan Choates, MS, CGC is the Assistant Program Director of the University of Texas Genetic Counseling Program and Assistant Professor in the Department of Obstetrics, Gynecology, and Reproductive Sciences at the McGovern Medical School at UTHealth Houston where she practices prenatal genetic counseling. She received a BS in Biochemistry and Genetics with a Minor in Psychology from Texas A&M University in 2014 and an MS in Genetic Counseling from the University of Texas Genetic Counseling Program in 2016. Meagan provides prenatal genetic counseling services at several Houston area clinics, and supervises genetic counseling students while on their prenatal rotation. In addition, she directs and teaches the genetic counseling program's Embryology course and Approaches to Genetic Counseling Research I & II. She co-directs and teaches in the program's Prenatal Genetic Counseling, Psychosocial Issues, and Psychosocial Practicum courses. She additionally oversees the genetic counseling students' Master of Science thesis research process. Her personal research interests include understanding how genetic screening and testing options are discussed, utilized, and interpreted in the clinical setting. ResearchGate profile: https://www.researchgate.net/profile/Meagan-Choates-2 In this segment we discuss: - The anecdotal observations that inspired the study, notably that low-risk and high-risk patients shared similar motivations for choosing NIPT. - That insurance coverage was the second most significant factor influencing the decision to undergo NIPT. - About 44% of participants were classified as making "uninformed decisions" despite receiving pre-test counseling from a genetic counselor. However, the term “uninformed” used by the MMIC tool can be misleading. - The challenge of balancing detailed knowledge expectations with patients' ability to make value-consistent and thoughtful decisions.   Would you like to nominate a JoGC article to be featured in the show? If so, please fill out this nomination submission form here. Multiple entries are encouraged including articles where you, your colleagues, or your friends are authors.   Stay tuned for the next new episode of DNA Dialogues! In the meantime, listen to all our episodes Apple Podcasts, Spotify, streaming on the website, or any other podcast player by searching, “DNA Dialogues”.    For more information about this episode visit dnadialogues.podbean.com, where you can also stream all episodes of the show. Check out the Journal of Genetic Counseling here for articles featured in this episode and others.    Any questions, episode ideas, guest pitches, or comments can be sent into DNADialoguesPodcast@gmail.com.    DNA Dialogues' team includes Jehannine Austin, Naomi Wagner, Khalida Liaquat, Kate Wilson and DNA Today's Kira Dineen. Our logo was designed by Ashlyn Enokian. Our current intern is Sydney Arlen.

In this episode we discuss the recent National Society of Genetic Counselor's Practice Resource on Dystrophinopathies, which was recently published in JoGC, with two of the publications' authors. You can find the Journal of Genetic Counseling webpage via onlinelibrary.wiley.com or via the National Society of Genetic Counselors website.   Segment 1: “Genetic counseling for the dystrophinopathies- Practice resource of the National Society of Genetic Counselors”   Ann Martin, MS, CGC is a board certified genetic counselor with Parent Project Muscular Dystrophy (PPMD). Ann serves as the VP of Community Research and Genetic Services and manages a team of genetic counselors who coordinate all aspects of The Duchenne Registry and the Decode Duchenne genetic testing program. Since joining PPMD in 2011, Ann has been directly involved in all aspects of the Registry programs including collection and curation of the Registry data, clinical trial and research study recruitment, data exports, patient and family inquiries, genetic testing, and educational content on the PPMD websites. Ann represents The Duchenne Registry on TREAT-NMD's Global Data Oversight Committee, which is responsible for reviewing requests for data from the TREAT-NMD Global Registries, and serves as the DMD Subgroup Co-Lead. In addition, Ann has been a member of Sarepta Therapeutics' Advisory Board for Early Diagnosis of Duchenne since 2022. Ann is continually engaging and educating both the patient and professional community about the Registry and Duchenne and Becker research. Before joining PPMD, Ann worked as a clinical genetic counselor for 15 years at Carolinas Medical Center in Charlotte, NC, where she provided genetic counseling for pediatric and adult patients with a wide range of genetic disorders. Ann is a graduate of the University of Cincinnati Genetic Counseling Graduate Program. She is board-certified by the American Board of Genetic Counseling and is a member of the National Society of Genetic Counselors. Angela Pickart (she/her) is a licensed, certified genetic counselor practicing in the Genomics Laboratory at Mayo Clinic, performing variant interpretation, report writing and test development for neurogenetics assays. She received her Master of Science degree in Genetic Counseling at the University of Minnesota and has extensive clinical experience in pediatric, neurology, and oncology genetic counseling prior to transitioning to her laboratory role. She has been awarded the academic rank of Assistant Professor of Laboratory Medicine at the Mayo Clinic College of Medicine and Science where she serves as course co-director of the Center for Clinical and Translational Sciences Molecular Variant Evaluation Course. She is also the course co-director of the Laboratory Practicum for the Medical College of Wisconsin Master of Science Genetic Counseling Graduate Program and Adjunct Assistant Professor of the Medical College of Wisconsin School of Graduate Studies.   In this segment we discuss: - Origins and significance of the genetic counseling-specific practice resource for dystrophinopathies. - Changes in the treatment landscape due to FDA-approved therapeutics and ongoing clinical trials for dystrophinopathies. - Strategies for educating patients and families about the implications of genetic testing and diagnosis in dystrophinopathies. - Advocacy roles of genetic counselors in helping patients access the latest therapies and participate in clinical trials for DMD/BMD. - Importance of interdisciplinary collaboration in managing dystrophinopathies and the roles genetic counselors play within these teams. - Potential broader impact of the practice resource on the medical field and patient community.    Would you like to nominate a JoGC article to be featured in the show? If so, please fill out this nomination submission form here. Multiple entries are encouraged including articles where you, your colleagues, or your friends are authors. Stay tuned for the next new episode of DNA Dialogues! In the meantime, listen to all our episodes Apple Podcasts, Spotify, streaming on the website, or any other podcast player by searching, “DNA Dialogues”.  For more information about this episode visit dnadialogues.podbean.com, where you can also stream all episodes of the show. Check out the Journal of Genetic Counseling here for articles featured in this episode and others.  Any questions, episode ideas, guest pitches, or comments can be sent into DNADialoguesPodcast@gmail.com.  DNA Dialogues' team includes Jehannine Austin, Naomi Wagner, Khalida Liaquat, Kate Wilson and DNA Today's Kira Dineen. Our logo was designed by Ashlyn Enokian. Our current intern is Sydney Arlen.

In this episode, we dive into the evolving landscape of talent attraction with Monica Hershberger and Kate Wilson from Role Call. As the world of work shifts, we explore how remote work has changed the game for communities and businesses striving to attract and retain top talent. Monica and Kate share their insights on the strategies that successful communities and companies are using, the role of quality of life and placemaking in talent retention, and how talent attraction efforts reflect a community's identity. Plus, we look into the crystal ball to discuss what the future holds for talent attraction strategy and economic development. 

Greg Maxwell & Kate Wilson/Jackson County Schools Work Based Learning Work-Based Learning (WBL) programs connect employers and schools to offer students unique opportunities that bridge classroom learning with real-world application. These experiences, which may be paid or unpaid, help students explore career interests, assess training needs, and cultivate the skills and mindset essential for […]

Greg Maxwell & Kate Wilson/Jackson County Schools Work Based Learning Work-Based Learning (WBL) programs connect employers and schools to offer students unique opportunities that bridge classroom learning with real-world application. These experiences, which may be paid or unpaid, help students explore career interests, assess training needs, and cultivate the skills and mindset essential for […] The post Greg Maxwell & Kate Wilson – Jackson County Schools Work Based Learning appeared first on Business RadioX ®.

In this episode we discuss two papers that highlight the importance of communication around family health history and the influence of family beliefs on genetic testing decisions. You can find the Journal of Genetic Counseling webpage via onlinelibrary.wiley.com or via the National Society of Genetic Counselors website.   Segment 1: ““Family health beliefs and cascade genetic testing in Asian families with hereditary cancer risk: “Okay, now what?””   Leena Tran began her career as a cancer genetic counselor at Cedars-Sinai in 2022, after completing her Master's of Science in Human Genetics and Genetic Counseling at Stanford University. Originally from Southern California, she is grateful to have the opportunity to work with patients and providers within the greater Los Angeles area. Leena is passionate about facilitating both provider and patient-directed education, as well as improving health care access and experiences for patients of diverse backgrounds.   In This Segment We Discuss: - The motivation behind exploring family health beliefs and cascade genetic testing in Asian families with hereditary cancer risk.. - Use of a constructivist approach in this study and rationale for choosing this methodology. - Influence of shared health beliefs within families on decisions regarding genetic testing and family communication. - Common strategies participants employed to discuss genetic testing with their relatives. - Roles genetics providers play in facilitating family discussions about cascade genetic testing.   Segment 2: “Young adults' reasoning for involving a parent in a genomic decision-making research study”   Dr. Melanie Myers is a Professor in the Division of Human Genetics, in the Department of Pediatrics, at Cincinnati Children's Hospital. She is the Co-Director of the Graduate Program in Genetic Counseling, a joint program between the University of Cincinnati and Cincinnati Children's Hospital. Dr. Myers has a background in public health genomics with specific training in genetic counseling, public health, social and behavioral sciences, and applied epidemiology. Her research interests include the impact of integrating genomics into public health research and practice. Dr. Myers's current NIH-funded work focuses on empowering adolescents from diverse backgrounds to participate in the decision-making process about learning genomic results. Myers obtained her MS in genetic counseling from the University of Cincinnati and her PhD in public health from the Johns Hopkins School of Hygiene and Public Health. www.cincinnatichildrens.org/geneticcounselingprogram   Julia Pascal is an oncology genetic counselor at Virginia Cancer Specialists. She earned her masters in genetic counseling from the University of Cincinnati genetic counseling program in 2023. Originally from the Washington DC area, Julia is grateful for the opportunity to care for cancer patients in the community where she grew up.    In This Segment We Discuss:   - Unique aspects of young adults' approaches to medical decisions compared to those of older adults. - Influence of cognitive maturity on young adults' readiness to make independent health decisions, particularly in complex fields like genomics. - Challenges encountered in designing a study that addresses both autonomous decision-making and parental influence. - Role of healthcare providers in supporting young adults' transition to independent decision-making.   Stay tuned for the next new episode of DNA Dialogues! In the meantime, listen to all our episodes Apple Podcasts, Spotify, streaming on the website, or any other podcast player by searching, “DNA Dialogues”.    For more information about this episode visit dna dialogues.podbean.com, where you can also stream all episodes of the show. Check out the Journal of Genetic Counseling here for articles featured in this episode and others.    Any questions, episode ideas, guest pitches, or comments can be sent into DNADialoguesPodcast@gmail.com.    DNA Dialogues' team includes Jehannine Austin, Naomi Wagner, Khalida Liaquat, Kate Wilson, and DNA Today's Kira Dineen. Our logo was designed by Ashlyn Enokian. Our current intern is Sydney Arlen.

In this episode we discuss a research study that focuses on Black women who tested positive for a pathogenic variant associated with an increased risk for breast cancer. You can find the Journal of Genetic Counseling webpage via onlinelibrary.wiley.com or via the National Society of Genetic Counselors website. Please note that the terminology used refers to women to reflect the language used in the paper, and all genders can have a risk to develop breast cancer. Segment 1: “A qualitative study of Black breast cancer previvors' and survivors' experiences after positive genetic testing” Malika Sud (she/her) is a genetic counselor who specializes in fetal genetics and rare disease diagnosis. She works at the Manton Center at Boston Children's Hospital, where her projects focus on discovering genetic causes of rare disease, improving access to genetic testing/counseling, and support around perinatal loss. She also cares for people with high-risk pregnancies at the Maternal Fetal Care Center at Boston Children's Hospital. Malika's work is informed by her community activism and lived experience as a woman of color - she is a longtime advocate for reproductive justice and strives to center marginalized voices healthcare and research. She teaches at the Boston University Genetic Counseling Program and serves on the NSGC J.E.D.I. Stewardship Committee in an effort to make the genetic counseling field more inclusive for patients and colleagues. Malika's Twitter handle is @malikasud   Erika Stallings is an attorney and writer based in Jersey City, NJ. In 2014 she learned that she carried a BRCA2 mutation and underwent a preventative mastectomy that same year. Since undergoing genetic counseling and testing she has worked to raise awareness of hereditary cancer with a specific focus on raising awareness in minority communities. Her writing about her experience with hereditary cancer as well as her work on health inequities has been published in NPR, O Magazine, The Cut, Jezebel and The New York Times. She is active on social media at the handle quidditch424 on X."  In This Episode We Discuss: - The origins of the study and the reasoning behind choosing this specific topic. - Erika's involvement as a patient advocate and how the team's diverse backgrounds shaped the research approach. - The five key themes uncovered in the study, with relevant participant quotes shared. - Insights on how healthcare providers can improve support for Black women with genetic results indicating higher breast cancer risk. - Discussion of the study's potential impact on future research and changes in clinical practice.   Stay tuned for the next new episode of DNA Dialogues! In the meantime, listen to all our episodes Apple Podcasts, Spotify, streaming on the website, or any other podcast player by searching, “DNA Dialogues”.    For more information about this episode visit dnadialogues.podbean.com, where you can also stream all episodes of the show. Check out the Journal of Genetic Counseling here for articles featured in this episode and others.    Any questions, episode ideas, guest pitches, or comments can be sent into DNADialoguesPodcast@gmail.com.    DNA Dialogues' team includes Jehannine Austin, Naomi Wagner, Khalida Liaquat, Kate Wilson, and DNA Today's Kira Dineen. Our logo was designed by Ashlyn Enokian. Our current intern is Sydney Arlen.

In this episode we discuss research on patient and family experiences in neurogenetics. You can find the Journal of Genetic Counseling webpage via onlinelibrary.wiley.com or via the National Society of Genetic Counselors website.    Segment 1: “Individuals' experiences in genetic counseling and predictive testing for familial amyotrophic lateral sclerosis” Connolly Steigerwald is a certified genetic counselor at NYU Langone Health's Division of Neurogenetics and Lysosomal Storage Disorders Program in NYC, where she assists in providing evaluations and genetic counseling for those with suspected or confirmed neurogenetic disorders. Her clinic population includes those with neurodevelopmental disabilities, epilepsies, neuromuscular disorders, dementias, white matter disorders, movement disorders, and lysosomal storage disorders. Connolly holds a Master of Science in Genetic Counseling from Columbia University, where she completed a specialty rotation in neurology with a focus on neurodegenerative and neuromuscular disorders such as amyotrophic lateral sclerosis. Her research interests include predictive genetic testing, lysosomal storage disorders, and implementation of genetic counselor led clinic models. Elizabeth Harrington, MS, CGC, is an ABGC board-certified genetic counselor and Lecturer in the department of Neurology at Columbia University. Ms. Harrington received her graduate degree in human genetics and genetic counseling from the Stanford University School of Medicine.  Ms. Harrington provides genetic counseling expertise in neuromuscular, neurodegenerative, and motor neuron diseases, and specifically provides clinical genetic counseling to patients and families with ALS. In addition to her clinical and academic responsibilities, Ms. Harrington directs the ALS Families Project research study, a presymptomatic natural history study designed to understand the genetic underpinnings of genetic forms of ALS and the impact on affected families. Link to the ALS Families Project: https://clinicaltrials.gov/study/NCT03865420 In this segment we discuss: How the experiences and decision-making processes for ALS risk compare to other neurodegenerative disorders, such as Huntington disease (HD). What influences individuals at risk for familial ALS/FTD to choose predictive genetic testing, including factors like religious affiliation. The psychological impact of testing positive for ALS-associated mutations is compared to those who test negative or opt out of testing, revealing significant emotional differences. Social support networks, whether from family, friends, or healthcare professionals, are critical for those processing genetic test results or managing their risk for ALS/FTD. The importance of integrating psychological care into the predictive genetic testing process to support individuals facing the risk of neurodegenerative diseases. Segment 2: “How parents of children with ataxia-telangiectasia use dynamic coping to navigate cyclical uncertainty” Victoria Suslovitch (Tori) is a genetic counselor and works as a genomic science liaison for the rare disease team at Ambry Genetics. She educates healthcare providers about genetic testing and genomic medicine, and aims to advance access, equity, and quality of genetics services. Prior, Victoria was a research genetic counselor at Boston Children's Hospital, for a study that develops genomically targeted therapies for children with rare neurological diseases. In this role, she worked closely with families of patients with ataxia telangiectasia. She received her Master of Science in Genetic Counseling degree from Boston University, and is certified by the American Board of Genetic Counseling.  Julia Schiller works as a cancer genetic counselor at AdventHealth in Parker, CO. She attended Drake University for her undergraduate degree, and Boston University School of Medicine for her genetic counseling degree and is certified by the American Board of Genetic Counseling. Originally from Minnesota, she now enjoys all the outdoor adventures Colorado has to offer with her partner, Adam, and their dog, Sprocket. Her passionate for health equity and preventative care drive her to create a space for patients where they feel empowered in their own healthcare. Link to the Ataxia Telangiectasia Children's Project (ATCP): https://atcp.org In this segment we discuss: Ataxia-Telangiectasia (A-T) - a pediatric movement disorder characterized by ataxia, immune deficiencies, and a higher risk of cancer, with symptoms often starting in early childhood. The similarities and differences in parental experiences as well as emotional and clinical challenges faced by families The five key themes that emerged: changes in parental responsibilities, shifts in family identity, evolving coping strategies, continuous uncertainty, and the importance of support from various sources. A-T's progressive nature meant that coping and identity changes were ongoing, with parents turning to connections with family, medical teams, and other A-T families. Parents described emotional, logistical, and financial challenges associated with the diagnosis, highlighting the need for supportive and understanding healthcare providers.   Stay tuned for the next new episode of DNA Dialogues! In the meantime, listen to all our episodes Apple Podcasts, Spotify, streaming on the website, or any other podcast player by searching, “DNA Dialogues”.    For more information about this episode visit dnadialogues.podbean.com, where you can also stream all episodes of the show. Check out the Journal of Genetic Counseling here for articles featured in this episode and others.    Any questions, episode ideas, guest pitches, or comments can be sent into DNADialoguesPodcast@gmail.com.    DNA Dialogues' team includes Jehannine Austin, Naomi Wagner, Khalida Liaquat, Kate Wilson, and DNA Today's Kira Dineen. Our logo was designed by Ashlyn Enokian. Our current intern is Sydney Arlen.

Screenwriter Stuart Wright talks to former film producer Kate Wilson about her debut novel PROSPECTS & the workplace culture app CALL IT! and "3 Films That Have Impacted Everything In Your Adult Life" BUGSY MALONE (1976)BACK TO THE FUTURE (1985)THE ACCUSED (1988)The novel PROSPECTS is out now https://www.prospects-novel.comFor more about the workplace culture app CALL IT! https://www.callitapp.org/about  "3 FILMS THAT HAVE IMPACTED EVERYTHING IN YOUR ADULT LIFE" is a podcast by screenwriter Stuart Wright that explores the transformative power of cinema. From emotional masterpieces to thought-provoking classics, each episode delves into the films that have had a profound impact on our personal growth and perspective. Through engaging storytelling, critical analysis, and cultural commentary, Stuart aims to uncover the lasting influence that movies have had on his guests. Please join him on an emotional journey through the world of film and discover how just three movies can change the direction of a life, cement memories you will never forget or sometimes change how you see the world."CreditsIntro/Outro music is Rocking The Stew by Tokyo Dragons (www.instagram.com/slomaxster/)Podcast for www.britflicks.com https://www.britflicks.com/britflicks-podcast/Written, produced and hosted by Stuart WrightSupport this podcast at — https://redcircle.com/britflicks-com-podcast/donationsAdvertising Inquiries: https://redcircle.com/brandsPrivacy & Opt-Out: https://redcircle.com/privacy

Guests include Megan Cho to discuss her paper, “Beyond multiple choice: Clinical simulation as a rigorous and inclusive method for assessing genetic counseling competencies” as well as Amanda Polanski and Ashley Kuhl to discuss their paper, “Leadership development in genetic counseling graduate programs.”   In this episode we discuss clinical training by exploring papers that discuss clinical simulation and leadership development. You can find the Journal of Genetic Counseling webpage via onlinelibrary.wiley.com or via the National Society of Genetic Counselors website.    Segment 1 “Beyond multiple choice: Clinical simulation as a rigorous and inclusive method for assessing genetic counseling competencies”   Megan is the Associate Director of the Johns Hopkins/NIH genetic counseling training program.  Prior to that, as the Research Program Manager at GeneDx, she created and led a team working to discover and describe rare genetic disorders.  Megan has practiced clinically at Columbia/New York Presbyterian Hospital and was also adjunct teaching faculty at the Sarah Lawrence College genetic counseling program.  She serves as the Co-Chair of the GCEA Education Committee, past Chair of the NSGC Outcomes Committee, past Chair of the NSGC Research Special Interest Group, and has been a member of various task forces including the NSGC Research Task Force and the ACGC Practice Based Competencies task force.   In this segment we discuss:  Challenges posed by standardized tests in ensuring equity. Alternative methods proposed in the article for assessing competence in new genetic counseling graduates and trainees. Contrasts between formative and summative assessments in simulation-based education. Differences in assessment difficulty and methodology between genetics knowledge and counseling competence. Barriers and challenges in implementing simulation in large-scale certification exams in other fields.   Segment 2 “Leadership development in genetic counseling graduate programs”   Amanda Polanski is a certified genetic counselor at Minnesota Perinatal Physicians. She graduated from the University of Wisconsin-Madison Master of Genetic Counselor Studies program in 2023, and her research focused on characterizing the role of leadership development in genetic counseling graduate programs. Previously, she has done research on identification and diagnosis of familial hypercholesterolemia through the University of Minnesota. She currently enjoys providing compassionate and inclusive care to prenatal patients alongside other dedicated providers.   Ashley Kuhl, MS, CGC, is the Assistant Program Director at the Master of Genetic Counselor Studies program at the University of Wisconsin-Madison and an assistant professor (CHS) in the Department of Pediatrics. She enjoys working with genetic counseling and other health professions learners in various capacities and with patients and families in the UW Biochemical and Medical Genetics clinics at the Waisman Center. She began her clinic work in 2013 after completing her master's degree in Medical Genetics from the UW-Madison Genetic Counseling Training Program.   In This Segment  We Discuss: Enhancement of genetic counselors' impact through leadership skills. Importance of intentional leadership development in advocating for patients and the profession, and the role of genetic counseling in broader healthcare advocacy efforts. The variation in the definition and understanding of leadership among program leaders, and its impact on leadership development within genetic counseling (GC) programs. Role of faculty in driving leadership development and effective strategies employed to instill leadership skills in GC students. Identification of current leadership development as a top area for improvement and actionable steps for programs to address this gap.   [Plug guest website and SM]   Would you like to nominate a JoGC article to be featured in the show? If so, please fill out this nomination submission form here. Multiple entries are encouraged including articles where you, your colleagues, or your friends are authors.   Stay tuned for the next new episode of DNA Dialogues! In the meantime, listen to all our episodes Apple Podcasts, Spotify, streaming on the website, or any other podcast player by searching, “DNA Dialogues”.    For more information about this episode visit dnadialogues.podbean.com, where you can also stream all episodes of the show. Check out the Journal of Genetic Counseling here for articles featured in this episode and others.    Any questions, episode ideas, guest pitches, or comments can be sent into DNADialoguesPodcast@gmail.com.    DNA Dialogues' team includes Jehannine Austin, Naomi Wagner, Khalida Liaquat, Kate Wilson and DNA Today's Kira Dineen. Our logo was designed by Ashlyn Enokian.   

Guests include Gina Sanchez to talk about her paper, “Status of abortion curriculum in genetic counseling: Survey of graduate programs and recent graduates in the United States” and Dr. Holly Rankin to discuss her paper, “Termination counseling among US perinatal genetic counselors in the setting of second trimester fetal anomalies.”   Segment 1: Gina Sanchez, MS, MB(ASCP), CGC is a genetic counselor and Instructor in the Department of Obstetrics, Gynecology, and Reproductive Sciences at the McGovern Medical School at The University of Texas Health Science Center at Houston. She received a BS in Zoology from Texas Tech University in 2012, a MS in Molecular Pathology from Texas Tech University Health Sciences Center in 2013, and a MS in Genetic Counseling from The University of Texas Genetic Counseling Program in 2022. Gina provides prenatal genetic counseling services in both English and Spanish at several Houston area clinics. She is a member of the National Society of Genetic Counselors and the Texas Society of Genetic Counselors. Gina's research interests include genetic counseling education and increasing access to genetic counseling care for the Spanish-speaking patient population. In this segment, we discuss: Assessment of the abortion curriculum in genetic counseling graduate programs and the study participants. Variability in the amount and types of abortion training across surveyed programs. Factors influencing the training provided. Greater satisfaction and preparedness among graduates from programs with a dedicated abortion curriculum. Notable discrepancies between responses from recent graduates and program representatives. Key topics highlighted as important parts of abortion education. Variability in clinical training as a barrier to abortion education and potential solutions to standardize this education. Segment 2: Dr. Holly Rankin received her undergraduate degree in anthropology, graduating summa cum laude, from the University of California, Los Angeles. She completed her medical education at Sidney Kimmel Medical College at Thomas Jefferson University, Philadelphia where she was inducted into the Gold Humanism and the Alpha Omega Alpha Honor Societies. Dr. Rankin completed her residency training in Obstetrics and Gynecology at Johns Hopkins University, Baltimore. She received the Ryan Program Excellence in Family Planning Award at the end of residency training. Dr. Rankin is excited to be a Complex Family Planning fellow at UC Davis and plans to focus her career on providing abortion and contraceptive specialty care to underserved, rural communities. In this segment, we discuss: The impact of state laws and location on counseling and termination options. Differences between genetic counselors and other healthcare providers in handling these cases. Balancing patient autonomy with counseling challenges. How reproductive justice affects the discussion of termination options, especially with changing abortion laws.   Follow us on Instagram @dnadialoguespodcast and on LinkedIn at Journal of Genetic Counseling.   Stay tuned for the next new episode of DNA Dialogues! In the meantime, listen to all our episodes Apple Podcasts, Spotify, streaming on the website, or any other podcast player by searching, “DNA Dialogues”.    For more information about this episode visit dnadialogues.podbean.com, where you can also stream all episodes of the show. Check out the Journal of Genetic Counseling here for articles featured in this episode and others.    Any questions, episode ideas, guest pitches, or comments can be sent into DNADialoguesPodcast@gmail.com.    DNA Dialogues' team includes Jehannine Austin, Naomi Wagner, Khalida Liaquat, Kate Wilson and DNA Today's Kira Dineen. Our logo was designed by Ashlyn Enokian. Our current intern is Sydney Arlen.  

In this episode we discuss navigating non-invasive prenatal screening, also known as non-invasive prenatal testing, by reviewing two articles covering genetic counseling insights, informed consent challenges, and inclusive practices. You can find the Journal of Genetic Counseling webpage via onlinelibrary.wiley.com or via the National Society of Genetic Counselors website.    Segment 1 “Genetic counseling for fetal sex prediction by NIPT: Challenges and opportunities”   Chelsea Stevens is a clinical and research genetic counselor in the cardiovascular genetics clinic at Brigham and Women's Hospital. She has been working at BWH since 2022 and works primarily on projects aimed to understand genotype/phenotype relationships in cardiomyopathies. The publication we will be discussing today is the result of Chelsea's capstone project during her genetic counseling graduate education at the MGH Institute of Health Professions. She is from Connecticut and has been living in Boston for the past 6 years and loves working in a city with a strong genetic counseling network.   Courtney Studwell  is a laboratory genetic counselor in the Center for Advanced Molecular Diagnostics (CAMD) at Brigham and Women's Hospital. In the cytogenetics laboratory, Courtney serves as a liaison to clinical providers ordering genetic testing and helps to implement updated testing protocols that reflect patient needs and the evolving landscape of genetic testing technologies. In addition to working in the laboratory, Courtney also sees patients in the Center for Fetal Medicine and Reproductive Genetics at Brigham and Women's Hospital and is passionate about providing high-quality genetics care to patients at all stages of their reproductive process.   In this segment, we discuss: An overview of NIPS, its evolution and recommendations on utilizing it as a screening tool Insights into study participants' clinical practices and training regarding inclusive language for sex and gender Challenges and misconceptions faced by providers when offering NIPS Recommendations to address issues related to challenges and misconceptions   Segment 2 "What knowledge is required for an informed choice related to non-invasive prenatal screening?"   Jill Slamon is an Assistant Professor in Obstetrics and Gynecology in the Vanderbilt School of Medicine and the founding Assistant Program Director of the Vanderbilt University Master of Genetic Counseling Program. Jill has over 12 years of clinical experience in reproductive and prenatal genetic counseling with unique experiences in preconception counseling in the queer community. Her research interests focus on topics ranging from genetic counseling education and training, genetic counseling outcome measures, patient-reported outcome measures, and experiences of queer patients seeking preconception and prenatal care. Jill earned a Bachelor of Science from the Lyman Briggs College at Michigan State University. She then earned a Master of Art in Teaching from National Louis University and a Master of Science in Genetic Counseling from Northwestern University in Chicago, IL.   In this segment, we discuss: The challenges in informed consent and fetal sex prediction in NIPS Professional guidelines related to informed consent and NIPS The multidimensional measure of informed choice (MMIC) Impact on decisional conflict among patients offered NIPS   Would you like to nominate a JoGC article to be featured in the show? If so, please fill out this nomination submission form here. Multiple entries are encouraged including articles where you, your colleagues, or your friends are authors.   Stay tuned for the next new episode of DNA Dialogues! In the meantime, listen to all our episodes Apple Podcasts, Spotify, streaming on the website, or any other podcast player by searching, “DNA Dialogues”.    For more information about this episode visit dnadialogues.podbean.com, where you can also stream all episodes of the show. Check out the Journal of Genetic Counseling here for articles featured in this episode and others.    Any questions, episode ideas, guest pitches, or comments can be sent into DNADialoguesPodcast@gmail.com.    DNA Dialogues' team includes Jehannine Austin, Naomi Wagner, Khalida Liaquat, Kate Wilson and DNA Today's Kira Dineen. Our logo was designed by Ashlyn Enokian. 

Kate Wilson - Vail Resorts - Y on Earth Community Podcast The post Episode 164 – Kate Wilson, Vail Resorts, VP of Environmental & Social Responsibility first appeared on Y on Earth Community.

In our fourth episode, we delve into the importance of gender-inclusive language in genetic counseling and the specific challenges transgender and gender-diverse (TGD) individuals face in accessing hereditary cancer care. You can find these articles in a special virtual issue of the Journal of Genetic Counseling which is free and open access for the month of June. You can find the Journal of Genetic Counseling webpage via onlinelibrary.wiley.com or via the National Society of Genetic Counselors website.    Segment 1 “Use of gender-inclusive language in genetic counseling to optimize patient care”   Heather Motiff graduated with a B.S. in Psychology from the University of Wisconsin-Whitewater in 2006. She has extensive experience working as a crisis response advocate and co-facilitating support groups for survivors of intimate partner violence. Heather discovered her interest in genetic counseling during her first pregnancy in 2010. She has served as a Community Resource Specialist and contributed significantly to gender-affirming care initiatives during her graduate studies at UW-Madison. Heather is now an oncology genetic counselor at SSM Health Cancer Care in Madison, WI, and is dedicated to providing inclusive, quality healthcare and genetic services.   In this segment we discuss: Specific examples and terms used in gender-inclusive language. Comfort levels of genetic counselors with using gender-inclusive language. Findings from thematic analyses on the use of gendered language and its impact on patient care. Suggestions for additional training resources for healthcare professionals. Segment 2 “Experiences of hereditary cancer care among transgender and gender diverse people: “It's gender. It's cancer risk…it's everything”   Sarah Roth is a genetic counselor and a PhD candidate in Anthropology at Johns Hopkins University. She is a BRCA1 carrier whose research focuses on the experiences of patients, communities, and providers in cancer care and genomic medicine. Sarah has been a founding editor of Tendon at JHU's Center for Medical Humanities & Social Medicine, a contributing writer at Synapsis: A Health Humanities Journal, and a recent predoctoral fellow in Bioethics at the National Institutes of Health.   In this segment, we discuss: Challenges faced by TGD individuals in accessing hereditary cancer care. Participants' perspectives on gendered language in healthcare. Actionable recommendations for healthcare providers to support TGD individuals with hereditary cancer syndromes.   Would you like to nominate a JoGC article to be featured in the show? If so, please fill out this nomination submission form here. Multiple entries are encouraged including articles where you, your colleagues, or your friends are authors.   Stay tuned for the next new episode of DNA Dialogues! In the meantime, listen to all our episodes Apple Podcasts, Spotify, streaming on the website, or any other podcast player by searching, “DNA Dialogues”.    For more information about this episode visit dnadialogues.podbean.com, where you can also stream all episodes of the show. Check out the Journal of Genetic Counseling here for articles featured in this episode and others.    Any questions, episode ideas, guest pitches, or comments can be sent into DNADialoguesPodcast@gmail.com.    DNA Dialogues' team includes Jehannine Austin, Naomi Wagner, Khalida Liaquat, Kate Wilson and DNA Today's Kira Dineen. Our logo was designed by Ashlyn Enokian. 

Can the corporate veil be protected? In our latest podcast, Kate Wilson, a Professional Support Consultant in our London Real Estate team, is joined by Alex Wright, a Senior Associate in our Corporate Real Estate team, and Somers Brewin, Vice-President in the Transactional Risk team at Lockton, to discuss the potential liabilities that can arise on corporate acquisitions pursuant to the Building Safety Act 2022, and the ways in which the insurance market is adapting to address these risks.

To celebrate DNA Day we are releasing our April episode exploring concepts related to the diagnostic odyssey, whole genome sequencing, and results returned.    Segment 1: A Journey of Hope and Resilience   In our first segment, we delve into the research conducted by Celine Lewis, focusing on the emotional impact of receiving a "no primary finding" (NPF) result from genome sequencing. This recent JoGC paper is titled, “The disequilibrium of hope: A grounded theory analysis of parents' experiences of receiving a “no primary finding” result from genome sequencing.”   Celine's study uncovers the multifaceted journey of parents grappling with the absence of a definitive diagnosis for their children. Through grounded theory analysis, two primary themes emerge: "Striving to Solve the Unsolved Puzzle" and "Navigating Hope, Lost then Found." These themes encapsulate the oscillating emotions of hope, disappointment, and resilience experienced by parents amidst the diagnostic odyssey.   Dr. Celine Lewis is a behavioural scientist working in the field of genetic and genomic medicine. She is currently at University College London Institute of Child Health, and is an NIHR Advanced Fellow. Her work focuses on how patients and families relate to, communicate and make decisions around personal genetic information, and the subsequent behavioural, psychological and social outcomes.    Through her research, Celine has worked with a range of key stakeholders including researchers in the UK and abroad, healthcare professionals and policy makers as well as voluntary organisations, patients and families. She is regularly invited to present at UK and international conferences and meetings and is increasingly asked to present her research findings to organisations such as NHS England and the Department of Health.   Key Insights from Segment 1: - The importance of understanding the emotional dimensions of genetic testing, especially for families receiving inconclusive results. - The dynamic role of hope as both a motivator and a coping mechanism throughout the diagnostic journey. - Suggestions for pre and post-test counseling strategies to support families navigating genomic testing, emphasizing the significance of managing expectations and fostering adaptive hope.   Segment 2: Systematic Review of Secondary Findings   In our second segment, we explore a systematic review conducted by Lucas Mitchell and Dr. Amanda Willis, focusing on the uptake and outcomes of returning secondary findings to research participants. This recent JoGC article is titled, “Systematic review of the uptake and outcomes from returning secondary findings to adult participants in research genomic testing.”   Through rigorous analysis of existing literature, Lucas and Amanda illuminate key insights into the prevalence of secondary findings and their psychological, medical, and ethical implications. Their review underscores the critical role of researchers in navigating the complexities of result return, highlighting considerations for enhancing participant engagement and support.   Lucas Mitchell is a research genetic counsellor at the Garvan Institute of Medical Research in Sydney, Australia. He contributes to the My Research Results genetic counselling platform, an evidence-based service that supports researchers in delivering actionable research genomic findings to participants nationwide. With a Master of Genetic Counselling from the University of Technology Sydney, Lucas is passionate about helping participants and their families in understanding their research findings and facilitating access to ongoing support. Lucas's current research interests lie within the application of genomics and returning secondary findings, and the intersection of genetic healthcare with diverse communities and improving inclusion and accessibility.   Dr. Amanda Willis is a research genetic counsellor at the Garvan Institute of Medical Research. After completing a Master of Genetic Counselling in 2013, Amanda worked as a cancer genetic counsellor in Australia and the UK and completed a PhD in 2018. Amanda's current work is centred around the My Research Results program, developed to help research participants access their genetic information. Amanda provides genetic counselling to research participants who receive a genetic result and conducts research to understand the experiences of these participants. Through this work, she aims to increase access to genomic information and improve outcomes for research participants and their families.   Key Insights from Segment 2: - The significance of secondary findings in research genomic testing and the need for comprehensive strategies to address participant needs. - Key findings regarding the uptake of secondary findings and diverse outcomes experienced by research participants. - Implications for researchers, healthcare providers, and policymakers in optimizing result return processes and promoting participant well-being.   As we conclude our exploration, it becomes evident that genetic testing transcends the realm of science, delving deep into the intricacies of human emotions and resilience. Through the insightful research of our guests, we gain valuable insights into the lived experiences of individuals navigating genetic testing, offering a glimpse into the profound impact of hope, disappointment, and adaptive coping mechanisms.    Stay tuned for the next new episode of DNA Dialogues! In the meantime, listen to all our episodes Apple Podcasts, Spotify, streaming on the website, or any other podcast player by searching, “DNA Dialogues”.    For more information about this episode visit dnadialogues.podbean.com, where you can also stream all episodes of the show. Check out the Journal of Genetic Counseling here for articles featured in this episode and others.    Nominate your articles, or a colleagues, here and we may feature it on the show! Any questions, episode ideas, guest pitches, or comments can be sent into DNADialoguesPodcast@gmail.com.    DNA Dialogues' team includes Jehannine Austin, Naomi Wagner, Khalida Liaquat, Kate Wilson and DNA Today's Kira Dineen. Our logo was designed by Ashlyn Enokian. 

In our second episode, we explore two recent articles focusing on the intersection of the disability community and genetic counseling training and practice.    Segment 1: “Disability education and implications for genetic counselor training”   Lauren Douglas (she/her) serves as an oncology genetic counselor and supervisor for graduate student rotations at MHealth Fairview in Minneapolis, MN. She received a degree in Genetic Counseling from the University of Texas MD Anderson Cancer Center UTHealth Graduate School of Biomedical Sciences in 2021. Outside of work, she finds joy in practicing yoga, enjoying the outdoors, and cheering on her favorite Minnesota sports teams.   Chelsea Wagner (she/her) is a seasoned genetic counselor specializing in prenatal and reproductive health. She is the outgoing chair for NSGC's Prenatal Special Interest Group and serves as reproductive health expert for NSGC's media panel. She is currently a Lead Genetic Counselor at BillionToOne. Chelsea identifies as a person with a disability courtesy of a brain injury acquired in 2019 and her experience living with chronic illness for almost two decades.    Segment 2: “Experiences of genetic counseling students with disabilities and chronic illnesses: A qualitative study”   Rachel Epstein (she/her) is a 2022 graduate of the Boston University Genetic Counseling Program. She is currently working as a genetic counselor in the Neaman Center for Personalized Medicine at Endeavor Health in Evanston, IL, where she works primarily in adult cancer genetics.   During the episode we recommending the following resources: NSGC Member Webinar Series: 2023 Community Conversations  Disability in Genetic Counseling Group on Instagram @disabilitygc or email disabilitygc@gmail.com   Would you like to nominate a JoGC article to be featured in the show? If so, please fill out this nomination submission form here. Multiple entries are encouraged including articles where you, your colleagues, or your friends are authors.   Stay tuned for the next new episode of DNA Dialogues! In the meantime, listen to all our episodes Apple Podcasts, Spotify, streaming on the website, or any other podcast player by searching, “DNA Dialogues”.    For more information about this episode visit dnadialogues.podbean.com, where you can also stream all episodes of the show. Check out the Journal of Genetic Counseling here for articles featured in this episode and others.    Any questions, episode ideas, guest pitches, or comments can be sent into DNADialoguesPodcast@gmail.com.  DNA Dialogues' team includes Jehannine Austin, Naomi Wagner, Khalida Liaquat, Kate Wilson and DNA Today's Kira Dineen. Our logo was designed by Ashlyn Enokian.

ROI serves as an important benchmark for all life sciences companies, whether it involves a pipeline candidate, new products, or marketing strategies. But what does ROI have to do with creating a culture of care?In this episode of Moving Forward, Giving Back, our guests Troy Wilson, CEO of Kura Oncology, Kate Wilson, President of the Gilead Foundation, Matt Gline, CEO of Roivant, and Tom Croce, Vice President of Global Patient Advocacy at Jazz Pharmaceuticals join host Morgan Berman, Executive Director of Life Science Cares Philadelphia, to explore how creating a culture of care ensures overall business success, achieves a competitive advantage within their specific business landscape, creates a supportive work environment for employees, and maintains a genuine, distinct corporate identity.This is an insightful, information rich conversation on an essential topic that you do not want to miss. To learn more go to lifesciencecares.org.

Welcome to the first episode of DNA Dialogues! Today is February 29th, 2024. It is a leap year, so today marks an extra special rare disease day.    Rare diseases can impact so many people - from patients themselves, to families, to broader communities. To celebrate rare disease day, we are going to dive into two recent articles from the Journal of Genetic Counseling that showcase the rare disease experience. The following interviews provide insight into the wider impact of rare disease, with a special focus on families.   Segment 1: “Understanding type and quality of relationships between individuals with chromosome 18 syndromes and their siblings”   Dr. Catherine Larson joins us in the first segment to talk about her recent article titled, “Understanding type and quality of relationships between individuals with chromosome 18 syndromes and their siblings”.    Dr. Catherine Larson is a Child and Adolescent Psychiatrist and a sibling to Elizabeth, who has a Chromosome 18 deletion. After earning her undergraduate degree, she worked as a research assistant at the Chromosome 18 Research Center, where she began her research on Sibling relationships. Dr. Larson earned her Medical Degree from the University of Texas School of Medicine at San Antonio. She then went on to complete a General Psychiatry Residency Program, followed by a Fellowship in Child and Adolescent Psychiatry at The University of Texas at Austin, Dell Medical School. As a practicing psychiatrist, she opened her private practice in Austin, Texas, and she also returned to join the research team at the Chromosome 18 Research Center.   Dr. Catherine Larson is double Board Certified by the American Board of Psychiatry and Neurology in General Psychiatry and Child and Adolescent Psychiatry. Dr. Larson earned her Medical Degree from the University of Texas School of Medicine at San Antonio. She then went on to complete a General Psychiatry Residency Program, followed by a Fellowship in Child and Adolescent Psychiatry at The University of Texas at Austin, Dell Medical School. In addition to her private practice, she is currently an Adjunct Assistant Professor at The University of Texas Health School of Medicine at San Antonio.  Segment 2 “Families' experiences accessing care after genomic sequencing in the pediatric cancer context: ‘It's just been a big juggle'”   Authors Sarah Scollon and Blake Vuocolo talk about their recent Journal of Genetic Counseling paper in the pediatric cancer space.    Sarah Scollon is an Assistant Professor in the Department of Pediatrics at Baylor College of Medicine and certified genetic counselor for the Texas Children's Hospital Cancer Genetics and Genomics Program. She has served in dual clinical and research roles across the course of her career. Her research interests engage the overarching themes of (1) adaptation of genetic counseling practice to implement evolving technologies (2) optimization of patient-provider communication and education and (3) equity and inclusion for diverse populations in genetic medicine and research. Ms. Scollon has had a longstanding dedication to the care of children and families affected by cancer. She is an advocate for including genetic counseling into pediatric cancer care. She works to educate others on the role genetics and genomics can play in the care of patients with pediatric cancer and their families both from a clinical and psychosocial standpoint.   Blake Vuocolo is a certified research genetic counselor in the Department of Molecular and Human Genetics at Baylor College of Medicine. She graduated from the Baylor College of Medicine Genetic Counseling Program in 2022, and her thesis work focused on access to follow-up hereditary cancer care in underserved pediatric populations through the KidsCanSeq study. Currently, her work focuses on exome and genome sequencing of medically underserved populations with undiagnosed diseases throughout Texas. Ms. Vuocolo is passionate about finding sustainable ways to improving genomic health equity worldwide. Her interests include exploring access barriers to receiving genomic care in different healthcare contexts and improving genetics education for non-genetics healthcare providers in under resourced regions of the country and beyond.   Stay tuned for the next new episode of DNA Dialogues! In the meantime, listen to all our episodes Apple Podcasts, Spotify, streaming on the website, or any other podcast player by searching, “DNA Dialogues”.    For more information about this episode visit dnadialogues.podbean.com, where you can also stream all episodes of the show. Check out the Journal of Genetic Counseling here for articles featured in this episode and others.    Any questions, episode ideas, guest pitches, or comments can be sent into DNADialoguesPodcast@gmail.com.    DNA Dialogues' team includes Jehannine Austin, Naomi Wagner, Khalida Liaquat, Kate Wilson and DNA Today's Kira Dineen. Our logo was designed by Ashlyn Enokian. 

Joe speaks with Kate Wilson, Associate Advisor at Matthews + Associates, about an essential topic of estate planning: preplanning and prepaying for your funeral.   Kate stresses the importance of thoughtful consideration of one's end-of-life wishes, encouraging you to document your preferences and keep them alongside your estate planning documents. While the topic may not be the most lighthearted, Joe and Kate offer practical insights, aiming to empower listeners to make informed decisions about their final arrangements.    Read the full show notes and find more information here:  EP 67 Show Notes

Thu, 14 Dec 2023 13:00:00 +0000 https://efm-industry-insights.podigee.io/46-innovative-production-tools-shaping-the-future-of-filmmaking a5a2f18a026c4cd62c93feb78002370b Industry Insights – The EFM Podcast is presented by the European Film Market of the Berlinale. Hosted by strategist, conference curator, moderator & speaker AC Coppens, it delves deep into the rapidly evolving film industry. In this episode, EFM Startups Alumni Kate Wilson, Volha Paulovich, and John Mahtani delve into the realm of innovative tools for the film industry. They share valuable insights on recognising and responding to industry needs, as well as navigating the challenges of introducing new tools to the market. Additionally, they express their perspectives on current developments in the film industry and discuss maintaining a balance between technical advancements and fostering creativity. Volha Paulovich is a dynamic force in the world of technology and storytelling, combining her passion for both to create truly awe-inspiring experiences. With an impressive background in advertising, game development, and commercial video production, she has honed her skills in crafting captivating narratives that leave a lasting impact. As a co-founder of PentoPix, Volha is currently at the helm of a team that harnesses the power of artificial intelligence to revolutionize the way stories are brought to life. By seamlessly transforming movie scripts into editable 3D animated videos, she is spearheading a new era of creativity and efficiency. PentoPix has gained worldwide recognition and support from esteemed film studios, directors, producers, and renowned film festivals such as the European Film Festival, Berlinale, and SXSW, where it has claimed double awards for being the best in entertainment, media, and content. Volha's unwavering dedication to innovation and commitment to pushing the boundaries of storytelling make her a true trailblazer in her field. John Mahtani is a Chartered Accountant with commercial & financial experience within the Media industry, extensive global network across Europe, North America, Middle East, & Asia. He held corporate roles at Warner Bros, Paramount Pictures, and Universal Pictures, before Co-founding Cinelab London. Currently John is the CEO of Drylab Media Tech group plc - a SAAS platform servicing film and tv productions globally. Kate Wilson works in film and TV as a writer, producer and consultant. She worked with the Film and TV Charity on their mental health project and Covid relief strategy, raising more than £9M from industry partners. She is a graduate of UCLA and RADA and a Member of the Bar of England and Wales. The host AC Coppens is a strategist, conference curator, host, moderator & speaker. They founded THE CATALYSTS, an agency for innovative & creative players working at the crossing of Digital Tech, Film/XR, Music/Sound, Design & Culture, to turn conferences into sites of knowledge exchange and co-creation. The Berlinale's European Film Market is the first international film market of the year, where the film industry starts its business. Industry Insights - The EFM Podcast puts a spotlight on highly topical and trendsetting industry issues, thereby creating a compass for the forthcoming film year. The year-round podcast is produced in cooperation with Goethe-Institut and co-funded by Creative Europe MEDIA. full no EFM,Film Industry,European Film Market,Startups,PentoPix,Drylab,Call it,Production Tools,AI,Technology European Film Market

This is the story of an engineering rebel who embraced Auburn sight unseen, fell in love with Aubie, broke Oxford's generational curse on her family, and tackled the greatest challenges for green infrastructure. Eat your heart out, Ole Miss.Listen to the award-winning #GINNing gang's interview with junior Kate Wilson, the new president of Auburn's chapter of the American Society of Civil Engineers (ASCE).

For the month of October, applications are open for YOU to become a TFI Advocate, bridging the gap between foster care agencies and churches right in your local community. This only happens twice a year! Learn more and apply here. If you've ever had a dream in your heart, you know there can be a lot of steps to make it a reality. Along the way, you will likely encounter hardships, delays, and doubts. I have a special treat for you today as we have not one, but two guests! Kate Wilson is the Founder and CEO of Foster + Heart, a Non-Profit in Idaho that is dedicated to igniting the community to meet the needs of children in foster care. Even though the journey was long towards realizing her dream, God set things in motion to not only place that calling on her life early on but also see it come to fruition. Secilia “Cece” Bedolla is a former foster youth and team member at Foster + Heart. Experiencing an incredibly challenging and traumatic upbringing, Cece's story is a story of discovering hope in the midst of hardship. I was so honored to have this conversation and I hope it's an encouragement to you this week! Listen in as they share how God guided their circumstances and gave them the experience to meet the needs of children in foster care today. Show Notes: https://theforgotteninitiative.org/wilson-bedolla-205/

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BWNO: Bias Breakers - Archna Gohil & Kate Wilson | Archna Gohil and Kate Wilson's turn in this 6-part series of Bias Breakers, focussing on the recent anthology with 12 authors released on 19th April 2023, today's segment covers two stories by two women of differing heritage converging on their womanhood. Both taking routes to self-actualisation through their study and entrepreneurial efforts. You can purchase your copy of the book here: Bias Breakers (Dr Andrea Malam BEM) - https://amzn.to/43wIYh2 Episode Sound Partner: Seasalt.ai --- Send in a voice message: https://podcasters.spotify.com/pod/show/curious-anarchy/message

The first report from a seven-year inquiry into undercover policing in England and Wales has been published, finding that undercover policing deployments were unjustified and would have been "brought to a rapid end" if the public had known what was going on. First commissioned in 2015 by then Home Secretary Theresa May, the investigation is aiming to discover the truth about undercover policing over the past 50 years and provide recommendations for the future. On the Sky News Daily with Niall Paterson, our Home Editor Jason Farrell explains the history of ‘spycops' that led to the inquiry, and Kate Wilson, an environmental activist who was deceived into a two-year intimate relationship by an undercover police officer in 2003, talks about her experience. Producer: Soila Apparicio Interviews producer: Alex Edden Editor: Danielle Weekes-Chilufya

Relax with a calming mix of music and natural sounds, from the Atlantic rainforests of Brazil to Eastern Banjo Frogs in Adelaide, Australia. Plus a dawn chorus in Cornwall and chaffinches in Noja, Northern Spain. Recordings by BBC Radio 3 Sunday Breakfast listeners Bob Castell, Kate Wilson, Peter Halmkin and Kevin Cox.

Caroline Harleaux & Lee Andrews en direct de Manchester ! Leurs invités ce mois-ci sont Iyun et Sam, un duo qui opère sous le nom de GOMID, et mixent electronica, beats, hip-hop et folklore, avec une intensité fascinante.TracklistGOMID - GOGOMID - Tongueoyamao – IrohaLil Yachty – running out of timeClub Eat – BlueBABYXSOSA – MONEY BAGS IN THE TRUNKDreams – Chill Lo-fi Algorithms To Study ToIceboy Violet – this ain't rain it's an avalancheCOI LERAY – FLY SH1TLEVI CARTER – NOT TRYNA LINKQOVŌP – So ColdYoung Fathers – Tell SomebodyBuju - Many Ways feat. WizkidIan Isiah – 247Sachio Fujioka, Manchester Camerata, John Barrow, Joe Houghton, Kate Wilson, Jonathan Price & Kyoko Tabe – Dream Colored Mobile II, Op. 58aLianne Le Havas – Read My MindJapan – GhostsFlorence Sinclair – snow bunnyOZOMATECUHTLI – TEOTIHUACANOSPerfume Genius & Nídia – Moonbend (Nídia Remix)Chunky – Dancin' on TablesAir Max '97 – Work To LiveSeyi Vibez – Para Boi Hébergé par Acast. Visitez acast.com/privacy pour plus d'informations.

Caroline Harleaux & Lee Andrews en direct de Manchester ! Leurs invités ce mois-ci sont Iyun et Sam, un duo qui opère sous le nom de GOMID, et mixent electronica, beats, hip-hop et folklore, avec une intensité fascinante. GOMID - GO GOMID - Tongue oyamao – Iroha Lil Yachty – running out of time Club Eat – Blue BABYXSOSA – MONEY BAGS IN THE TRUNK Dreams – Chill Lo-fi Algorithms To Study To Iceboy Violet – this ain't rain it's an avalanche COI LERAY – FLY SH1T LEVI CARTER – NOT TRYNA LINK QOVŌP – So Cold Young Fathers – Tell Somebody Buju - Many Ways feat. Wizkid Ian Isiah – 247 Sachio Fujioka, Manchester Camerata, John Barrow, Joe Houghton, Kate Wilson, Jonathan Price & Kyoko Tabe – Dream Colored Mobile II, Op. 58a Lianne Le Havas – Read My Mind Japan – Ghosts Florence Sinclair – snow bunny OZOMATECUHTLI – TEOTIHUACANOS Perfume Genius & Nídia – Moonbend (Nídia Remix) Chunky – Dancin' on Tables Air Max '97 – Work To Live Seyi Vibez – Para Boi

Joining Nadia in the studio for this episode of the ground-breaking Women of FinTech Podcast is Kate Wilson, Global Head of Consumer Deposits and Payments at RFI Global.Kate's tenure at RFI Global is well beyond the average often seen across our industry. We explore why Kate has stayed at RFI Global for over 10 years; from exposure and the opportunity to engage with a variety of roles, to the evolving growth-orientated culture, we gain an exclusive insight into the retention strategy at the company.The pair go on to discuss DE&I at industry events, sharing what it takes to empower voices often underrepresented in financial services panel discussions. Presenting and public speaking wasn't an inevitable engagement for Kate; but with the right support structures and positive training, Kate was elevated to feel comfortable as a public speaker. We gain insight into the further actions we can take to roll the latter approach out to the entire marketplace.And Kate also reminds us of the importance of ensuring our approach to inclusion is reflective- not one crafted by an isolated group. This will undoubtedly innovation in FinTech as we begin to speak to an inherently more diverse consumer-base.Kate's thoughts on family policies at companies is also highly revealing of the work we all still need to do to #walkthetalk for change across the entire industry.Thank you Kate for joining us on the Women of FinTech Podcast!

Erin is joined by Kate Wilson, managing editor of the Vancouver Tech Journal, to check-in on Collision Conference, the Olympics of Tech. More than 340 women-led startups were featured 39% of speakers were women, up 9% from 2019 Over 44% over attendees were women 2022 featured the Indigenous Atendee Program for the first time

In Season 4, Episode 2 of the Global Digital Banker Podcast, RFI Global's Kate Wilson discusses the exciting role embedded finance plays in today's banking ecosystem, and what the future holds for Railsbank, with COO, APAC Ben Smith.   Subscribe to our RFI Global channel and get notified when we have new episodes: https://youtu.be/M7lpAK6Itao  Connect with Ben Smith on LinkedIn: https://www.linkedin.com/in/bensmithprofile/  Connect with Anna Shaw on LinkedIn:  https://www.linkedin.com/in/anna-perera-shaw-966530129/  Connect with Kate Wilson on LinkedIn: https://www.linkedin.com/in/kate-wilson-5448667b/    To learn more about RFI Global, visit: https://rfi.global/

Vaxa Group communications specialist Kate Wilson explains more. See omnystudio.com/listener for privacy information.

This week it's Talicza's turn to share a UK story where women fought back and also this week, Talicza and Rachael are in the same room for the first time! From Los Angeles, Talicza tells the story of Kate Wilson and how she, along with several other women, fought against Mark Kennedy and other police officers after they were deceived in an undercover operation. Like what you're hearing? Leave a rate and review in Apple Podcasts and let us know what you think by visiting us on our socials: Instagram: @transatlanticcrime Twitter: @transatcrimepod Facebook: facebook.com/transatlanticcrime Patreon: patreon.com/transatlanticcrime Want to support us even more? Check out our merch store: https://www.redbubble.com/shop/ap/59763237 And our booklist: https://bookshop.org/shop/transatlanticcrime

In Season 4, Episode 1 of the Global Digital Banker Podcast, RFI Global's Anna Shaw sat down with Volt Bank's CEO and Founder, Steve Weston. In this short session they discuss his extensive experience of the banking industry, innovation and the history of Volt Bank and what's next.   Subscribe to our RFI Global channel and get notified when we have new episodes. Connect with Steve Weston on LinkedIn:  https://www.linkedin.com/in/steve-weston-b5102166/  Connect with Anna Shaw on LinkedIn:  https://www.linkedin.com/in/anna-perera-shaw-966530129/  Connect with Kate Wilson on LinkedIn:  https://www.linkedin.com/in/kate-wilson-5448667b/   To learn more about RFI Global, visit: https://rfi.global/  

Episode No. 539 features artist Stephanie Syjuco and historian Kate Wilson. Stephanie Syjuco's work is featured in several exhibitions around the United States. The Amon Carter Museum in Fort Worth is presenting "Stephanie Syjuco: Double Vision," a site-specific commission that builds from the Carter's collection to investigate historical and art historical narratives around American imperialism in the West. The project was curated by Kristen Gaylord and will be on view through January 2023. Syjuco is also in "Futures," a 32,000-square-foot pan-Smithsonian exhibition on view at the Smithsonian's Arts & Industries building through July 6; "Constellations: Photographs in Dialogue" at the San Francisco Museum of Modern Art through August 21; and "Stephanie Syjuco: Latent Images" at New York's Ryan Lee Gallery through March 12. Syjuco works across media such as installation and photography to investigate how images have helped build racialized, exclusionary narratives that have helped construct history and determine citizenship. Among the institutions that have presented her projects and solo exhibitions of her work are the Baltimore Museum of Art, the Blaffer Art Museum, the Contemporary Art Museum Saint Louis, the University of Kentucky, the Cantor Arts Center at Stanford University, and the Asian Art, Havana and Bucharest biennials. Wilson is a senior lecturer in the Department of Classics in Arts & Sciences at Washington University in St. Louis. Last semester she taught a class called "Race and Identity in Greco-Roman Antiquity." Concurrently she organized a teaching gallery exhibition in Wash U's Kemper Art Museum titled, "Colonizing the Past: Constructing Race in Ancient Greece in Rome." The project was the rare presentation of whiteness studies-informed exhibition in American art museum. Instagram: Stephanie Syjuco, Tyler Green. 

Four weekly audio stories in February & March from The Writers' Block, Writers Room. Pencarrow Suit by Kate Wilson Kate Wilson writes short stories and flash fiction. Her favourite writers are 1) Kevin Barry 2) Lucia Berlin and 3) Deborah Eisenberg although this order changes regularly depending whose work she's reading. She also loves George Saunders. Kate completed an MA in Creative Writing at Exeter University in 2021. Read by Nina Hills, Olivia Lowry, Aidan Nightingale & Keith Sparrow. Directed by Connie Crosby Audio recording & production by Phil Innes. 

David Chaviano welcomes Kate Wilson again. This time she gives an overview on what RISE with SAP is and what learning content is available on SAP Learning Hub and other sources. Kate is an experienced trainer and learning room lead on SAP Learning Hub with focus on SAP S/4HANA private and public cloud edition as well as RISE with SAP.

In this episode David Chaviano welcomes Kate Wilson, experienced trainer and learning room lead on SAP Learning Hub with focus on SAP S/4HANA private and public cloud edition. Kate gives a brief introduction what SAP S/4HANA essentially is and shares insights for new and experienced learners on how to get started, staying current and certified as well as how to make best use of the digital learning opportunities in SAP Learning Hub.

In this week's episode, Kate Wilson speaks to FIS' Head of Banking Solutions APAC, Adrian Toynton, to get his thoughts on the accelerated digitialisation of the banking sector as a result of the pandemic. With a focus on Core Platform Modernisation and Cloud Migration, this chat dives into the tech powering big banks, the need for banks to address their aging core systems as a priority and what the future holds for the industry in ANZ. FIS Report: https://empower1.fisglobal.com/digitalization-and-cloud-migration.html?utm_campaign=BS_LBGL_MB_PM_TPP_RFI_DEC2021_WP_BANKMODERNIZATIONRFI%5bT

The COVID-19 pandemic continues to affect the pediatric community. With the return to school and the surge in pediatric COVID-19 cases, young children face challenges they've never met before, both at school and home. Join host Dr. Vanessa Raabe and special guest Abby Hollis, a Certified Child Life Specialist at Children's Healthcare of Atlanta, as they discuss the challenges facing young children today and highlight various strategies and resources that parents, teachers, and healthcare workers can use to help kids cope with COVID-19 during the pandemic.Questions or comments for NETEC? Contact us: info@netec.orgFind us on the web: netec.orgHostVanessa N. Raabe, MDAdult and Pediatric Infectious Disease Physician at NYU Grossman School of MedicineGuestAbby HollisCertified Child Life Specialist at Children's Healthcare of AtlantaResourcesAssociation of Child Life Professionals: https://www.childlife.orgCoronavirus, a Book for Children, written by Elizabeth Jenner, Kate Wilson and Nia Roberts. FREE DOWNLOAD at https://stayhome.candlewick.comNETEC COVID-19 Novel Coronavirus Resources: https://repository.netecweb.org/exhibits/show/ncov/ncovNETEC COVID-19 Webinar Series Playlist: https://www.youtube.com/playlist?list=PL5JyGXQ8MP0TZXU2Ldy-jzjLuUNfFX8JZNETEC Resource Repository: https://repository.netecweb.org

This third part on the legal action taken relating to undercover police officer Mark Kennedy at the Investigative Powers Tribunal. This episode looks at the actual trial of Kate Wilson's Human Right's claim at the High Court. Part 1 (Episode 6): https://soundcloud.com/spycops/episode-6-kate-wilson-the-ipt-part-1 Part 2: (episode 16): https://soundcloud.com/spycops/kate-wilson-the-ipt-part-2 Look out for the 4th and final part of this mini-series once the judgement of the Tribunal is handed down. hopefully before the end of 2021.

Kate and Ben return to talk more about the case Kate brought to the Investigative Powers Tribunal, you can hear part one here: https://soundcloud.com/spycops/episode-6-kate-wilson-the-ipt-part-1 You can learn about her case at the Investigative Powers Tribunal: https://campaignopposingpolicesurveillance.com/kate-wilson-case-exposing-institutional-sexism-spycops/ Follow Kate on twitter: https://twitter.com/fruitbatmania Please support the pod by ordering some stickers: https://ko-fi.com/s/df86432870

Core Participants in the Undercover Policing Inquiry Kate Wilson and Ben have a wide ranging chat with their neighbour Brian on the topic. This episode serves as useful introduction to those not familiar with the details of the whole issue. For Kate Wilson's story check out: https://policespiesoutoflives.org.uk/our-stories/kates-story/ Kate and Ben first appeared in episode 6 talking about the legal case Kate brought to the Investigative Powers Tribunal: https://soundcloud.com/spycops/episode-6-kate-wilson-the-ipt-part-1

Majestic Horses: Live at The Bearded Lady, West End, 16 November 2019 Majestic Horses are a three-piece led by Kellie Lloyd, a long-time lynchpin of the Brisbane music community who has played in such bands as White Mansions, Warm Guns, DEAFCULT and Screamfeeder. On record, Majestic Horses are made up of Lloyd on vocals and guitar, Andrew P Street on bass and Kate Wilson on drums. Howerver, due to each member living in a different state they have taken on many different incarnations when playing live. The set you'll hear in this episode featured Lloyd, Imogen Kowalczyk on bass and Nathan Crust on drums. In 2019 the Majestic Horses released their debut album, "Away From The Sun". Includes an interview with Kellie Lloyd. Recorded by Nell Forster & Scott Mercer Mixed by Jack B-Jones Special thanks to live engineer Nell Forster Show production, engineering and host: Scott Mercer Originally aired via Zed Digital, 7-8pm, Sunday 22 August, 2021

We have an exciting episode for everyone today! We are joined by Dr. Kate Wilson. Dr. Wilson is a holistic healthcare practitioner; she deals with manual osteopathy (the structure of the body.) Today we talk about who we are- not just a physical 3D body, but cover the mind, body, and soul. To learn more about Dr. Kate Wilson visit her website at: http://integralhealingwellness.com/Follow Us:Facebook https://www.facebook.com/AwakeningConsciousnessAJInstagram https://www.instagram.com/awakeningconsciousnessaj/YouTube https://www.youtube.com/channel/UCljw7ae6Nrwfi8oJ30r14YwBitchute https://www.bitchute.com/channel/zdtnY6dXNSJr/Brand New Tube https://brandnewtube.com/@AwakeningConsciousness_AJRumble https://rumble.com/c/c-891787Gab https://gab.com/AwakeningConsciousnessAJMeWe https://mewe.com/p/awakeningconsciousnesswithasherandjesseJoin our Telegram Chat: https://t.me/AwakeningConsciousness_AJOur Websites:https://drtomcowan.com/https://www.drcowansgarden.com/https://www.abecuador.com/

Latest Spoken Label Session features the wonderful Kate Wilson. More details about Kate can be read at: http://katejwilson.co.uk/ Her collection be can bought on Wildpressbooks at: http://www.wildpressedbooks.com/one-night-in-january.html and can be puchased on Amazon for £1.99 (sterling) Pieces read out in this session include: 1. Mount Esja 2. America 3. Yearning 4. Anecdote 5. Sunflowers 6. Lessons

Join Dr. Mark Sylvester and Dr. Richard Schulman as they speak with Dr. Kate Wilson on how the world went crazy in the last year and how we're going to restore it to sanity. It's a sweet discussion about creating harmony between ourselves and the natural world.

Join Anna Shaw and Kate Wilson as they discuss financial wellness and inclusion. Joined by Mariko Braswell from Move78 and Dr. Vinita Godinho from Financial Resilience Australia as they discuss the challenges that generations are facing with their financial wellbeing. They discuss their partnership to create the APAC Financial Wellness Initiative as well as their global alliances.    Hosts:  Anna Shaw - Head of Client Insights. RFi Group Kate Wilson - Research Director and Deputy GM AUNZ, RFi Group   Producer:  Taylor Henderson - Marketing Manager, RFi Group

Guest: Kate Wilson In the latest episode of what has become known as 'the soap war', the advertising regulator has ruled that Protex still can't be advertised as a soap that can 'naturally protect against germs' because of its flaxseed oil ingredient. In February, the regulator gave Colgate-Palmolive, the company that makes Protex, 3 months to amend its packaging so that it did not make the claim. The case was brought against it by competitor Reckitt Benckiser, which manufactures soap products under the Dettol brand. We speak to Kate Wilson, a chemical engineer who works in product development at Rain Natural Skincare, which makes soaps and natural body products. See omnystudio.com/listener for privacy information.

Kate Wilson was one of the women deceived into to a relationship by undercover police officer Mark Kennedy. Like several others she brought a civil claim against the police about it, unlike anyone else she was able to finally get a day in court about it. You can read her personal story here: https://policespiesoutoflives.org.uk/our-stories/kates-story/ Learn about her case at the Investigative Powers Tribunal here: http://campaignopposingpolicesurveillance.com/2021/04/24/kate-wilson-case-exposing-institutional-sexism-spycops/ And follow her on twitter here: https://twitter.com/fruitbatmania This is just part one of what is likely to be a very long running series, look out for part two in the months ahead.

病毒來勢洶洶，我們到底該怎麼辦？ 新型冠狀病毒究竟是什麼？ 如何傳染？如何預防？ 感染後的症狀是什麼？有治療的方法嗎？ 本書以孩子能理解的語言， 傳遞我們每個人在這段非常時期都必備的醫學常識， 即時解答關於疫情的許多疑問。 本書選自《病毒來了，我該怎麼辦？》三民書局出版 作者：Elizabeth Jenner , Kate Wilson , Nia Roberts 繪者：Axel Scheffler 翻譯：三民書局編輯部 Powered by Firstory Hosting

Today if you are a woman you are likely to live into your eighties. But what to do with those extra couple of decades? Dawn French is best known for her comedy and acting and is now an author long listed for the Women’s Prize. She talks about reinvention and still being relevant at any age. Kate Wilson talks about her court case against the Metropolitan Police and the National Police Chiefs Council. She's taking the legal action because she fell in love with a man who wasn't who he said he was. He was an undercover policeman whose job was to infiltrate environmental protest groups. Women's Football is seeing a huge growth in interest and exposure but there's some concern that the commentary of women's matches is too soft on mistakes and ends up sounding patronising. Ben Bloom, Telegraph sports columnist and commentator and Jacqui Oatley commentator and founding member of Women in Football discuss whether commentary should become more critical as the success of the game develops. Nazanin Zaghari Ratcliffe has been sentenced to another year in an Iranian prison and has been banned from travelling abroad. Her husband, Richard Ratcliffe talks about how Nazanin felt after hearing about the sentence and what it means for their family. Betty Webb MBE is 98 years old. During WW2 she worked at Bletchely Park and briefly at the Pentagon. She talks about promoting and remembering her war time experiences. How does the order in which we are born into our families affect us and our whole lives? The writer Lynn Berger discusses why people choose to have a second child and what does it mean to be one. Presenter: Anita Rani Producer: Paula McFarlane Editor: Lucinda Montefiore

Arlene Foster, First Minister of Northern Ireland and leader of the DUP, has stood down. She was the first woman and the youngest person to hold both jobs. In her resignation announcement she said that her election as leader of the Democratic Unionist Party broke a glass ceiling, and she also spoke about the trolling she's received. We discuss what her legacy will be. Kate Wilson has been giving evidence at The Royal Courts of Justice because she's suing The Metropolitan Police and the National Police Chiefs Council. She's taking legal action because she fell in love with a man who wasn't who he said he was. He was an undercover policeman who called himself Mark Stone. He was really Mark Kennedy whose job was to infiltrate environmental protest groups. Kate will have to wait until later in the year to get a result but she explains why she's taken the action. We talk to Kelly Critcher, who's a palliative care nurse. She works at the first hospital in the UK to declare a critical incident of Covid 19. She's written a book called A Matter of Life and Death: courage, compassion and the fight against the corona virus on the front-line. And do you share the bath water? TV property developer, Sarah Beeny, does. She gets in the bath after her husband and four sons. Sarah tells us why.

Season 3 is kicking off with our new hosts Kate Wilson and Anna Shaw!   

We had a really interesting chat with Emma-Kate Wilson about her journey into art writing through an Arts theory degree, writing art statements, and the importance for artists to be professionals. Thanks for speaking to us Emma-Kate.  After volunteering at a little ARI gallery in the Rocks, Emma-Kate decided to immerse herself in the visual language of Australia. In 2015, she embarked on a degree in Art Theory at UNSW and Art & Design in Paddington, Sydney, graduating in June 2018. Since then she has been published extensively in print and digital media, as well as working at some of Sydney's most prominent cultural institutions.Today, she can happily say, she is working full time as a freelance art and design journalist— including copywriting for renowned artists, designers, and publications.Emma-Kate writes regularly for Art Almanac, Artist Profile, Hunter & Folk, Est Living, Habitus Living, Domain Living, Ocula, MutualArt. She has also written for The Local Project, Vault, Articulate PR ( & The Golden Mean), Running Dog, un Projects, Art + Australia Online, Urban List, Art Monthly, ABC Arts, Lovatt's Media: Mindful Parenting & Audrey Daybook, Broadsheet, Concrete Playground, and Time Out. She also provides an awesome service for artists, writing copy for websites, statements etc. Get in touch with Emma through her website.

A lot of us build our photography business around what we think we "should" do to be successful and end up burnt out and broke as a result. What I’ve learned over the years and what I teach the photographers I coach inside of The Six Figure Studio is that the real secret to success comes from figuring out what YOU do, what your passion is, and then doing it fearlessly. In today’s episode, I’m talking with Toronto photographer Kate Wilson about this very thing. In our conversation, Kate shares how she freed herself from the "should" trap and instead built the foundations for her dream business. And best of all, she did it in just 90 days! Enjoy! SHOWNOTES: https://www.sandracoaneducation.com/podcast/letting-go-of-should And if you're ready to start building YOUR dream business? Download the Six-Figure Photography Framework. It will tell you what you need to focus on to turn your dreams into reality as well as what mistakes to avoid in the process. Follow this link to get your FREE copy! https://sandra-coan-photography.ck.page/c58ac67241

Meet Kate Wilson Somers, Sailor, Sailing Instructor and Entrepreneur. A life-long sailor, and sailing instructor, Kate has also been involved with the Volvo Ocean Race as support crew for Team Vestas 11th Hour Racing, the America's Cup with Oracle Team USA in 2012-2013, and The Rolex Big Boat Series in San Francisco.At the 24th Annual Providence Boat Show (2017), the Rhode Island Marine Trades Association recognized Kate as the Rhode Island Boater of the Year. Kate received that For the work she did to transform youth sailing programs to keep kids engaged, gain experience on some big boats, and boost and diversify the enrollment in these programs. In accepting the award, Kate chose to dedicate it to all the volunteers who work tirelessly to ensure these programs reach as many as possible.Kate is the Founder & Chief Designer of a marketing and web design company called RisingT Media and Marketing. Kate has worked with many clients including The Herreshoff Marine Museum. Storm Trysail Club, National Sailing Hall of Fame, Confident Captain, and many more. Learn more about Kate by visiting her website: risingt.com

Who would have thought that flax shives(husks) would present an opportunity to replace plastic in a wide range of consumer goods? In today’s episode, VP of Marketing Kate Wilson tells the story of the founding of Pela and how they are bringing a range of compostable consumer goods that aim to reduce our reliance on plastic day to day. She describes how a series of messy marketing experiments led to enhanced connection with their customers and a deeper sense of meaning within the company. KEY TAKEAWAYS FROM THIS EPISODEPersonal marketing is not an easy process, but it is so worth it for both customers and employees and creates amazing connections.You cannot automate relationships.Get personal. Feature your employees, be open, and use video to creatively connect with your customers. TODAY’S GUESTKate Wilson is VP of Marketing at Pela, the first compostable phone case company. She is deeply involved in every aspect of bringing the Pela brand to market at a time when we need alternatives to plastic more than ever.Find more about Pela on LinkedIn or visit their website at https://pelacase.com.Connect with Kate at LinkedIn. If you want to learn more about the eCommerce Growth Plan for your brand click here:https://mindfulmarketing.co/products/full-growth-planIf you've been paying attention and your brand is ready to GROW, apply now to be the one new brand we take on this month!https://mindfulmarketing.co/applyWant to join a network of founders and executives who know your unique challenges in scaling your E-com brand from 7 to 8 figures? Apply to join our Ecom Executives Mastermind here: https://Mindfulmarketing.co/mastermind

On this episode of the Deep Dive Podcast, Pastor Tracy Wilde-Pace sits down with Kate Wilson to talk about purpose and singleness. Kate is the mother of five children through adoption. Kate gives her testimony on having a grace for being a mother and trusting that God's timing is perfect and, at times, non-traditional. Email: CYAPodcast@capitalchurch.co Instagram: CapitalYoungAdults Music: www.purple-planet.com

Daniel Griffin provides a clinical report on COVID-19, then Amy joins us to discuss the 2020 Chemistry Nobel Prize for gene editing using CRISPR/Cas9, continuing circulation of poliovirus in Afghanistan, inborn errors of interferon in patients with severe COVID-19, and listener questions. Hosts: Vincent Racaniello, Alan Dove, and Rich Condit Guests: Daniel Griffin and Amy Rosenfeld Subscribe (free): iTunes, Google Podcasts, RSS, email Become a patron of TWiV! Links for this episode ASH guidelines on anticoagulants in COVID-19 patients (ASH) Followup of adults with noncritical COVID-19 (Clin Micr Inf) Tocilizumab in COVID-19 ICU patients (Lancet Rheum) Biological safety officer position at CUMC Support MicrobeTV at Parasites Without Borders 2020 Nobel Prize Chemistry (pdf) Progress towards polio eradication Afghanistan (MMWR) Inborn errors of IFN and serious COVID-19 (Science) Letters read on TWiV 671 Timestamps by Jolene. Thanks! Weekly Science Picks Amy - Coronavirus : A book for children by Kate Wilson and Nia Roberts Alan - Lost Prologue Rich -RAPS COVID-19 vaccine tracker Vincent - A Crack in Creation by Doudna and Sternberg and Sternberg on TWiM 184 Intro music is by Ronald Jenkees Send your virology questions and comments to twiv@microbe.tv

Daniel Griffin provides a clinical report on COVID-19, then Amy joins us to discuss the 2020 Chemistry Nobel Prize for gene editing using CRISPR/Cas9, continuing circulation of poliovirus in Afghanistan, inborn errors of interferon in patients with severe COVID-19, and listener questions. Hosts: Vincent Racaniello, Alan Dove, and Rich Condit Guests: Daniel Griffin and Amy Rosenfeld Subscribe (free): iTunes, Google Podcasts, RSS, email Become a patron of TWiV! Links for this episode ASH guidelines on anticoagulants in COVID-19 patients (ASH) Followup of adults with noncritical COVID-19 (Clin Micr Inf) Tocilizumab in COVID-19 ICU patients (Lancet Rheum) Tech position with Dr. Rosenfeld Biological safety officer position at CUMC Support MicrobeTV at Parasites Without Borders 2020 Nobel Prize Chemistry (pdf) Progress towards polio eradication Afghanistan (MMWR) Inborn errors of IFN and serious COVID-19 (Science) Letters read on TWiV 671 Timestamps by Jolene. Thanks! Weekly Science Picks Amy - Coronavirus : A book for children by Kate Wilson and Nia Roberts Alan - Lost Prologue Rich -RAPS COVID-19 vaccine tracker Vincent - A Crack in Creation by Doudna and Sternberg and Sternberg on TWiM 184 Intro music is by Ronald Jenkees Send your virology questions and comments to twiv@microbe.tv

The coronavirus delayed the release of many books in the UK. In a couple of weeks, 600 new titles will come out all at once. Kate Wilson, Managing Director of Nosy Crow 00:36 #Book #Britain #Literature

Join Seth and Rebecca as they discuss their favorite books about how to talk to kids about the current pandemic and social distancing.  Show Notes: 3:00- Stay Inside Lil' Mouse, by Liz Russell 7:13- My COVID-19 Time Capsule, by Shaz Lambe 10:33- The Breaking News, by Sarah Lynne Reul 19:04-Coronavirus: A Book for Children, by Elizabeth Jenner, Kate Wilson, and Nia Roberts 35:03- Hello Lighthouse, by Sophie Blackall 43:57- Alma and How She Got Her Name, by Juana Martinez-Neal 44:00- A Big Mooncake for Little Star, by Grace Lin 44:05- Thank You Omu, by Oge Mora 44:13- The Rough Patch, by Brian Lies Find us on the web! Rad Child Podcast: www.radchildpodcast.com Facebook Twitter Instagram Contact us: radchildpodcast@gmail.com Be a guest Donate Buy Rad Merch Shift Book Box: https://www.shiftbookbox.com/ Facebook Instagram Twitter  

Hi everyone, we'd love you to give our new podcast a listen.Being Socially Distant is a new lockdown audio comedy from the producers of The Backstory Podcast. Written and produced by Tin Shed Productions and starring Suzy Coulson, Claire Mutimer, Kate Wilson and Ivan Vaughan. It is recorded remotely.You can listen to episode 1 here or click here to subscribe directly so that you get new episodes when they're released.Please follow us on instagram: @beingsociallydistantMusic: 'Latin Nights'Composer: Tim Brown, Brown House MediaPublisher: Pond 5Being Socially Distant is a Tin Shed Production. Hosted on Acast. See acast.com/privacy for more information.

This week Seth is joined by author and parent Meera Sriram and author and teacher Liz Russell as they discuss how to talk to kids about the current COVID-19 pandemic and social distancing. Show Notes: 9:03-COVID-19 Same & Different Social Story 9:50- Be a Coronavirus Fighter, by Songju Ma Daemicke 10:22- Coronavirus: A Book For Children, by Elizabeth Jenner, Kate Wilson, and Nia Roberts 11:38- Stay Inside Lil' Mouse, by Liz Russell 27:42- The Breaking News, by Sarah Lynne Reul 43:01- COVID-19 Time Capsule 51:51- Handwashing Video 52:37- Pepper & Soap Experiment 59:26- Society of Children's Book Writers and Illustrators 1:02:06- Author's Reading their Stories 1:04-25- The Yellow Suitcase, by Meera Sriram 1:05:00 A Gift For Amma, by Meera Sriram 1:05:23- Between Two Worlds, by Meera Sriram For More info about today's Guests: Meera Sriram www.meerasriram.com Liz Russell Instagram- @Minisculedeviations   Find us on the web! www.radchildpodcast.com Facebook Twitter Instagram Contact us: radchildpodcast@gmail.com Be a guest Donate Buy Rad Merch

Hamilton Perkins Collection Bags. In 2014, Hamilton Perkins founded Hamilton Perkins Collection, an independent brand, designing and producing unique and award winning bags and accessories from recycled materials. Hamilton Perkins Collection exists to create timeless limited edition bags made from recycled plastic water bottles, pineapple leaf fiber, and billboard vinyl. The result is that no two bags are ever the same. Our first design (pictured right), the Earth Bag Premium, was created so that our customers would not only carry a bag that was stylish but carry a bag they could be proud of. We surveyed more than 1,000 consumers to obtain their thoughts and feedback for each component of the Earth Bag Premium, which soon became one of our most popular designs. Perkins was the winner of the Virginia Velocity Tour hosted by the Governor of Virginia, and the recipient of a HUD Community Development Block Grant. The non-profit B Lab honored Hamilton Perkins Collection as a "Best for the World Overall" B Corporation in 2017. Hamilton Perkins Collection has been featured in Forbes, Fast Company, Money Magazine, and The Washington Post. The brand is currently offered in nearly 100 leading department stores and specialty stores in the United States, Canada, and Europe. https://hamiltonperkins.com/

Kate Wilson and Micky Yang from HSF's Real Estate and Corporate Real Estate teams discuss the proposed Registration of Overseas Entities Bill (which will require an overseas entity acquiring property in the UK to publicly register details of its beneficial owners) and the potential impact of the register on investment in UK real estate.

Certified genetic counselor Kate Wilson discusses both clinical care and insurance billing and coverage issues surrounding gene panel testing. Numerous studies have shown higher positive rates when testing with larger panels. Why do higher positive rates not necessarily lead to better insurance coverage? What will it take to get data showing a reduction in morbidity and mortality and demonstrating utility for medical management? Kate also provides insight into the complexities of billing for panels and the downsides of low-self pay pricing within an insurance-based healthcare system. Do you have questions or topics you’d like a genetic counselor to discuss on a future episode ? Leave us a short voice message here! We may use your message on a future show. Related Articles Robson M, Domchek S. “Broad Application of Multigene Panel Testing for Breast Cancer Susceptibility—Pandora’s Box Is Opening Wider.” JAMA Oncol. October 3, 2019.  Ray, Turna. “Concert Genetics Launches Software to Limit Coding Variability in Genetic Testing.”Genome Web. September 6, 2019.  Follow Kate on Twitter Connect with Kate on LinkedIn

Kate Wilson, Walk Manager for the Peoria Metro Walk to End Alzheimer’s discusses statistics and facts related to Alzheimer’s disease, plus what her organization is doing to help families impacted by it. She previews an upcoming charity event to help fight this disease.

From the Valley Episode 51 - Kate grew up in Peachester - spent a lot of time in Bundaberg before moving to Brisbane. Was Campbell Newman on Facebook for 3 years. Currently in her own business of Social Media Advisory. Gymast, Running, Mt Cootha, LNP - Great chat!

In this episode, Kate Wilson and Khalida Liaquat sit down with Nicole Bertsch, Jenny Morgan, and Patricia Birch to further explore the authors' recent articles in the Journal of Genetic Counseling and shed light on genetic counselors cultivating cultural safety with diverse patient populations.  For complete information on the speakers in today's episode, and on the NSGC Podcast series, visit https://www.nsgc.org/podcasts.  Don't forget to subscribe to the show!

For episode 50, I've looked back at the past year of interviews and put together a compilation of some of the best bits - or, at least, some memorable ones for me! In this episode, I look back at why people set up a publishing business, whether it's a small publisher, a tech business or something else. Reasons range from being made redundant, through frustration with how the industry works, to a simple passion for doing something else. This episode features extracts from interviews with Emma Barnes (episode 3), Alison Jones (episode 7), Ken Jones (episode 8), Bec Evans (episode 17), Justo Hidalgo (episode 18), Nancy Roberts (episode 20), Kate Wilson (episode 22), John Bond (episode 28) and Dominique Raccah (episode 29).

This week we take at look at how heightened customer expectations are really driving Buy Now Pay Later (BNPL) services across the Australian and New Zealand Markets. Guests include Tommy Mermelshtayn, Chief Strategy Officer at Zip Money and Kate Wilson, Research Director – Australia and New Zealand at RFi Group. Tommy shares an overview of the BNPL landscape, ZipMoney's customer centric approach, the impacts of regulation on the market, how they differentiate themselves and what they have planned for the near future. Kate shares data and insights into the trends within the BNPL space across awareness, usage, demographic variances, channel usage and satisfaction as well as the needs gap behind BNPL services and predictions around whether or not BNPL will displace other credit services available to consumers. The Global Digital Banker is an insight-backed podcast series focused on key trends, market insights, thought leadership and best practice within the fast growing and dynamic world of digital banking. www.globaldigitalbanker.com

This episode is brought to you by SharePoint Saturday Toronto where host Mark Kashman attended as keynote speaker and attendee. We talk with four leading Canadian SharePoint developers and consultants: Yana Berkovich, Vincent Biret, Kate Wilson and Sherman Woo. You'll hear their expertise and guidance on classic to modern migration, information architecture and taxonomy, Power BI, governance, and large-scale implementations of Microsoft Teams.   Running Time: 68min Show Intro [00:00:00:00] – SharePoint Saturday Toronto Guest Perspective – Roundtable Discussion with Vincent Biret, Kate Wilson, Sherman Woo and Yana Berkovich [00:02:22:00] Guest Perspective – SharePoint Saturday Toronto Sponsor Interviews with Habanero and Creospark [00:50:35:00] Article of the Week – SharePoint Look Book [01:01:30:00] Upcoming Events [01:03:35:00] Show Wrap [01:06:30:00]   Social and Info Links: SharePoint site SharePoint Community Blog SharePoint Facebook @MSSharePoint SharePoint Twitter@SharePoint Mark Kashman Twitter @mkashman Chris McNulty Twitter @cmcnulty2000 2toLead Twitter @2toLead Kanwal Khipple, CEO & Founder of 2toLead, Twitter @kkhipple, Eric Riz, Founder & CEO of Empty Cubicle, Twitter @RIZinsights and @empty_cubicle, Yana Berkovich, Microsoft Data Platform MVP, Data Solution Enabler Vincent Biret Twitter @baywet, Office Development MVP, Azure and Office 365 Developer at 2toLead Kate Wilson Twitter KwilsonTO, Office 365 Consultant at 2toLead Sherman Woo Twitter @SPSherm, Microsoft Office 365 Collaboration Specialist at MEC™ Habanero Twitter @HabaneroConsult Creospark Twitter @creospark   Resources: The Intrazone Audience Survey SharePoint "Look Book" aka.ms/SharePointLookBook   Upcoming Events: SPS Events and on Twitter @SPS_Events SharePoint Fest and on Twitter @SharePointFest  SharePoint Conference North America, May 21-23, 2019 Microsoft Ignite | The Tour   Subscribe to The Intrazone: Show Page: https://aka.ms/TheIntrazone Apple Podcasts Google Play Spotify Stitcher Overcast RadioPublic RSS

In the latest instalment of Bristol Live's podcast, our reporters discuss how South Bristol’s version of Hollywood is expanding, bumping into Poldark, the closure of one of the city’s most famous clubs and how student flats are taking over the city centre.Politics editor Kate Wilson is up first in the studio to talk about the breaking news this week that there are big plans for the Bottle Yard Studios in south Bristol, and the effect having such a world-renowned film and TV studio in the city has.Entertainment specialist Robin Murray is up next to talk about a big story in Stokes Croft - the closure of one of the city’s nightclubs, which has been announced.He talks about how the influx of student flats into this most trendy part of Bristol is actually changing the area to be less, er, trendy.If you have ever wished you could take a look inside your local newsroom and meet the team behind the headlines, Bristol Live have launched the perfect podcast for you.Every Friday, Bristol Live will give you an insight into the things happening in your area and give you exclusive access to the team.To listen to the podcast you can click here or alternatively download from wherever you get your podcasts. Just search ‘Inside Bristol Live’.You can also rate, review and subscribe to the podcast to make sure you don’t miss out.For anyone who wants to get in touch you can follow us on Twitter @ILBpodcast.You can rate, review and subscribe to the podcast on Apple Podcasts or wherever else you get your podcasts.   For information regarding your data privacy, visit acast.com/privacy

This weeks' episode focuses on the Financial needs of SMEs within the Australian market. Kate Wilson, Research Director - AU & NZ, RFi Group shares the data behind the current trends and the growth of alternative lenders in the Australia market. From a lender perspective, Beau Bortoli, CEO, Prospa discusses the biggest pain points for Australian SMEs and how Prospa differ from other lenders in the market. The Global Digital Banker is an insight-backed podcast series focused on key trends, market insights, thought leadership and best practice within the fast growing and dynamic world of digital banking. www.globaldigitalbanker.com

Kate Wilson is the Founder and CEO of Nosy Crow, an award-winning child-focused, parent-friendly publisher of children's books. Kate has an extensive pedigree in publishing, but her decision to start a publishing company has its roots in a professional crisis that she's turned to a comprehensive victory! In this episode, we talk about the need to know yourself as a Founder, and to surround yourself with people who will complement your strengths (and weaknesses), and about how even commercial failures can be a great source of pride. Kate's story also highlights the importance of finding a support network - whether that's people on a similar journey or even stories and books about those who've trod the path before us.

Robins On The Wire Episode 42 is a celebratory affair as Bristol City are granted planning permission for their upgraded training ground plans.Sky Sports' Michelle Owen and Bristol City reporter Gregor MacGregor discuss what this means and how important this is for the club while we also hear Lee Johnson's thoughts on the subject.The story behind Wednesday's planning decision is also examined in detail with local democracy reporter Kate Wilson providing the inside line from the planning meetings involving the club, with club CEO Mark Ashton making the case for upgrading Failand at a previous meeting. Wilson has sat in on all the official planning meetings and reveals what has been said so far, why there was a hold-up and the subsequent resolution.Meanwhile, Owen and MacGregor tussle over the line-up that the Robins should go for on Saturday, with Gregor revealing the thoughts of his colleagues from Yorkshire on the upcoming clash, as well as revealing that there is a good possibility of a new contract for one of Bristol City's starlets in the near future.The pair also turn their attention to the visit to the Hawthorns on Tuesday and also chew on the visit to Paul Cook's Wigan.Finally, the duo ponder why so few City games are on Saturdays in September and October. For information regarding your data privacy, visit acast.com/privacy

In this inaugural episode of the NSGC Podcast Series, hosts Khalida Liaquat and Kate Wilson sit down with Scott Weissman, MS, CGC; Jessica Greenwood, MS, LGC; and Dena Goldberg, MS, LCGC to discuss the importance of genetic counselors' involvement with social media.  For complete information on the NSGC Podcast series, visit https://www.nsgc.org/podcasts.  Don't forget to subscribe to the show!

Kate Wilson and Lucy Morton, lawyers in the Real Estate and Planning teams at HSF, provide a summary of the importance of marking documents with the words 'subject to contract' when entering a real estate transaction or joint venture arrangement, as discussed in the recent Court of Appeal case of Generator Developments v Lidl UK [2018] EWCA Civ 396

On this week's episode, Alex talks with digital editor Luke Beardsworth about what his job entails, how he got started in journalism and the age old issue of clickbait. Luke explains the importance of reporters being ingrained in their communities and, taking criticism from readers, and 'trending content'.Also on the show, Tristan Cork explains his latest project, the Bristol World Cup - his mission is to find one person from every country competing, bringing everyone together to celebrate Bristol and living here. It's a great idea and has received a lot of love across social media. Tristan explains where the idea came from, what the challenges have been so far and where he sees the project going in the near future.Lastly, Alex talks to Kate Wilson about her new role (a role that didn't exist a year ago) of being local democracy reporter. Funded by the BBC, Kate explains how it works and why it's important to communities across the region.Links to this episode's stories:Claims Bristolians can give '£150 an hour' to beggars at Temple Meads as city described as a 'soft touch'The Bristol World Cup If you'd like to follow us or any of the reporters featured in today's episode, here are the links:Inside Bristol Live: @IBLpodcastHost Alex Ballinger: @ambhackLuke Beardsworth: @LukeBeardsworthTristan Cork: @TristanCorkPostKate Wilson: @KWilson_journo For information regarding your data privacy, visit acast.com/privacy

Hangover cure by Ian Woolf, Michael Widjaja talks about bacteria using cleavage, Kate Wilson talks about building the virtual Penrith Observatory. Sound and facts checked by Charles Willock, Produced and hosted by Ian Woolf Support Diffusion by making a contribution bitcoin: 1AEnJC8r9apyXb2N31P1ScYJZUhqkYWdU2 ether: 0x45d2cd591ff7865af248a09dc908aec261168395

Special Guest & Owner of My Pretty Little Pretzel, Kate Wilson shares her story. Plus, we talk about top five pieces of advice for starting a food business. https://myprettylittlepretzel.com/

Join the DTRH gang for a festive special: a review of the year in children's books with YA author Melinda Salisbury, illustrator Steve Lenton and Nosy Crow publisher Kate Wilson. Including our favourite books of 2016, an interview with Guardian Children's Prize nominee Zana Fraillon, a feature on YA charity anthology I'll Be Home For Christmas, and readings from a new collection of stories, Winter Magic.

Twitter is a great way for real estate agents to stand out from the crowd. It doesn’t have to be complicated and it can be super effective. Learn how to get quick wins using this dynamic social media platform.

Kate WIlson is Chair of the Housing and Built Environment Forum and joint co-ordinator of the local Friends of the Earth group.

Whether you're new to Hampton Roads or a life-long resident, one of the best things about our region is the abundant, and delicious seafood. What's being done to prevent our coastal waters from overfishing and pollution? Has the oil spill in the Gulf of Mexico affected the seafood industry in Hampton Roads? We'll be joined by Virginia Marine Products Board executive director Mike Hutt, Kate Wilson from the Chesapeake Bay Foundation, and Karen Burns from the Virginia Aquarium. Plus, Jerry Bryan, owner of Coastal Grill in Virginia Beach will discuss how local seafood is an advantage and a challenge. HearSay's resident foodie, Patrick Evans-Hylton will get our mouths watering as he shares his seafood secrets as well.

Kate is senior at SMU and shares about how her relationship with Christ helped her overcome her addiction to alcohol