Join The Photo Detective, Maureen Taylor, each week as she discusses historical photos and how they fit into your family history. From ancestor identification to photo preservation, The Photo Detective Podcast covers it all. Featuring special experts from genealogy, fashion history, photo history, and restoration, it’s a not-to-miss for photo fans, genealogists, and lovers of history.
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Think Like a Founder is a series of conversations with leaders, thinkers, inventors, revolutionaries, problem-solvers, and smart, nice people. Hosted by Maureen Taylor, co-founder of SNP Communications, this podcast dives deeper into a founder’s mindset and mentality -- what makes them tick? The curiosity. The relentlessness. The crazy. The sacrifice. The loneliness. Host, Maureen Taylor (or Mo, as most know her) started SNP Communications with her husband, Renn Vara more than 25 years ago, ...
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A podcast for anyone interested in genealogy and who wants to learn how to document family history. Join Amy and Penny as we take you through our experiences in family history research.
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Rare Disease Advisor's Rare Care Podcast features exclusive interviews with experts and stakeholders from the rare disease community.
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Eyes On Whiteness is a podcast that illuminates the insidious and ignorant ways of whiteness, regardless of intent. Our guests are invited to talk about the ways white supremacy and patriarchy are pervasive and ever-present. Our conversations are rooted in a commitment to normalizing the "how, not if" lens for looking at the ways it's present for all of us.
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137: An Interview With Karin Hoelzer, DVM, PhD, Senior Director of Policy and Regulatory Affairs at NORD
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Larry Luxner, senior correspondent for Rare Disease Advisor, interviews Karin Hoelzer, DVM, PhD, senior director of policy and regulatory affairs at the National Organization for Rare Disorders (NORD). Dr. Hoelzer discusses the importance of convincing the US Congress to renew the Rare Pediatric Disease Priority Review Voucher Program, which is set…
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Preserving Your Legacy: Insights from Amanda Meeks of Permanent.org
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In this episode of The Photo Detective, host Maureen Taylor speaks with Amanda Meeks, the Community and Partnerships Manager at Permanent.org. They discuss the recent developments at Permanent.org, focusing on the Legacy Lab, a new program designed to help users create and publish public archives. The Legacy Lab includes an email course that breaks…
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Discussion on use of court records in genealogical researchBy The Two Blondes
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The Hidden History of Pockets: A Conversation with Hannah Carlson
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In this episode, Hannah Carlson, author of “Pockets: An Intimate History of How We Keep Things Close,” discusses the historical and social significance of pockets. Inspired by a personal experience where she had no pockets during an emergency, Carlson explores how pockets have evolved from medieval times to modern days, highlighting their gender di…
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136: An Interview With Susan Ward, PhD, Founder and Executive Director of the Collaborative Trajectory Analysis Project (cTAP)
15:32
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Larry Luxner, senior correspondent for Rare Disease Advisor, interviews Susan Ward, PhD, founder and executive director of the Collaborative Trajectory Analysis Project (cTAP), which seeks to broaden patient eligibility for clinical trials in Duchenne muscular dystrophy.By Rare Care Podcast
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Uncovering the Past Through Postcards with Maureen Taylor
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In this solo episode of Maureen Taylor’s podcast, “The Photo Detective,” Maureen delves into the captivating world of postcards. She explores their historical significance and practical uses, both as travel memorabilia and valuable tools in family history research. The episode highlights the evolution of postcards from the early 1900s, including th…
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135: An Interview With Taylor Kane, Founder and Executive Director of 'Remember the Girls'
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Larry Luxner, senior correspondent for Rare Disease Advisor, interviews Taylor Kane, founder and executive director of 'Remember the Girls.' The charity advocates for female carriers of X-linked rare disorders including Duchenne muscular dystrophy and hemophilia.By Rare Care Podcast
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134: An Interview With Dr. Jeffrey A. Cohen of the Cleveland Clinic on Cellular Therapies for MS
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Larry Luxner, senior correspondent for Rare Disease Advisor, interviews neurologist Jeffrey A. Cohen, MD, of Ohio's Cleveland Clinic on the latest developments in cellular therapies to treat multiple sclerosis.By Rare Care Podcast
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Discussion on genealogical research at the Library of Virginia.By The Two Blondes
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Threads of Life: Unraveling the Rich Tapestry of Sewing with author Clare Hunter
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Clare Hunter, author of “Threads of Life,” joins Maureen on The Photo Detective podcast. A Scottish native with a background in theatre, community art, and creative writing, Clare discusses her book, which intertwines memoir and history, highlighting the social, emotional, and political significance of sewing. “Threads of Life” explores the profoun…
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133: An Interview With Maureen Juip, Secretary of the Friedreich's Ataxia Research Alliance and Mother of 2 Children With FA
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101
The Hidden Stories of Tattooing: Dr. Matt Lodder on Tattoos in Photography and Society
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Dr. Matt Lodder discusses his book Painted People: 5,000 Years of Tattooed History on The Photo Detective podcast. Focuses on tattoo history post-photography, noting tattoos often didn’t show up in early photos. Tattoos were private, often hidden under clothing, and not commonly photographed. Lodder's interest in tattoos started from family stories…
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133: An Interview With Jacquelyn Bainbridge, DPharm, of the University of Colorado, on Cannabis Therapy for MS
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Larry Luxner, senior correspondent for Rare Disease Advisor, interviews Jacquelyn Bainbridge, DPharm, a neurology professor at the University of Colorado in Aurora, on the benefits of medical cannabis in treating multiple sclerosis.By Rare Care Podcast
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151
Discovering Civil War Ancestors Through Photography: Tips and Tools for Family Historians
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This solo episode of the “Photo Detective” podcast delves into the intriguing task of discovering photographs of Civil War ancestors. Host Maureen offers a wealth of strategies and resources that not only cater to finding Civil War soldier images but also generalize to uncovering historical family photographs. Emphasizing the personal connections a…
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132: An Interview With Michelle C. Werner, CEO of Alltrna
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131: An Interview With Dr. Flavia Nelson of the University of Miami on Treatment Options for NMOSD
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Larry Luxner, senior correspondent for Rare Disease Advisor, interviews Flavia Nelson, MD, director of the Multiple Sclerosis Center of Excellence at the University of Miami in Florida, on the difficulties of diagnosing neuromyelitis optica spectrum disorder.By Rare Care Podcast
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Discussion on preparations for onsite genealogical researchBy The Two Blondes
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Uncovering Manchester’s Dark Past: Dr. Dean Kirby on Angel Meadow and the Victorian Slums
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In this fascinating podcast episode, Dr. Dean Kirby, a historian, journalist, and professional genealogist based in Manchester, England, shares his deep-rooted interest in the Manchester slums. Key Inspiration: Discovery of great-great-great grandfather’s history in Angel Meadow, a notorious Manchester slum. Research Focus: Manchester slums during …
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130: An Interview With Kevin M. Flanigan, MD, Director of the Center for Gene Therapy at Nationwide Children's Hospital in Columbus, Ohio
10:06
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Larry Luxner, senior correspondent for Rare Disease Advisor, interviews Kevin M. Flanigan, MD, director of the Center for Gene Therapy at the Abigail Wexner Research Instute of Nationwide Children’s Hospital in Columbus, Ohio. The subject of our talk is exon skipping therapies for Duchenne muscular dystrophy.…
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How Storied.com Transforms Family History into Captivating Stories
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In this episode of “The Photo Detective,” host Maureen Taylor welcomes Kendall Hewlett, CEO of Storied.com, to discuss the revolutionary platform that fills a crucial gap in the family history industry by emphasizing the importance of storytelling over mere data collection. Inspiration Behind Storied.com: Kendall Hewlett created the platform to foc…
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129: An Interview With Durresamin Khan, Pakistani Mother of a Boy With Duchenne Muscular Dystrophy
8:31
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Larry Luxner, senior correspondent for Rare Disease Advisor, interviews Durresamin Khan, the Pakistani mother of a boy with Duchenne muscular dystrophy, about the difficulties of obtaining treatment for DMD patients who are ineligible for gene therapy.By Rare Care Podcast
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128: An Interview With Jenny Huang, Mother of SMA Patient and MIT Math Whiz Benjamin Lou
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Larry Luxner, senior correspondent for Rare Disease Advisor, interviews Jenny Huang, whose son, Benjamin Lou, is an award-winning math major at MIT who also has spinal muscular atrophy.By Rare Care Podcast
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How to Manage and Remove Duplicate Photos for Genealogy Projects
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In this solo episode of Ask Maureen, I’ll address a common genealogist’s dilemma: managing and organizing digital photos, including handling duplicates. Whether you’re a seasoned genealogist or a beginner, mastering photo organizers and duplicate detection tools can simplify your work and enhance your family history projects. Key Topics Importance …
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127: An Interview With Omer Abdul Hamid, MD, of Nemours Children's Hospital in Orlando, Florida
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Larry Luxner, senior correspondent for Rare Disease Advisor, interviews Omer Abdul Hamid, MD, a neurologist at Nemours Children's Hospital in Orlando, Florida, on gene therapy's potential to treat Duchenne muscular dystrophy.By Rare Care Podcast
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Episode 98 - Stake Your Claim: Genealogy Gold in Homestead Records
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Discussion on using homestead records in genealogical research.By The Two Blondes
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126: An Interview With Pamela Gavin, New CEO of the National Organization for Rare Disorders (NORD)
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14:23
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Larry Luxner, senior correspondent for Rare Disease Advisor, interviews Pamela Gavin, the newly appointed CEO of the National Organization for Rare Disorders (NORD).By Rare Care Podcast
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Exploring Ancestry.com’s New Photo and Storytelling Features with Crista Cowan
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Today, I am thrilled to have Crista Cowan, Ancestry.com’s Corporate Genealogist, also known as “The Barefoot Genealogist” on YouTube, as our guest. Crista has been a pivotal figure at Ancestry, helping countless people uncover their family histories. Introduction of the “Memories” feature, previously known as “Storymaker Studio.” Details on how use…
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125: An Interview With Patricia Weltin, Founder and CEO of Beyond The Diagnosis
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17:59
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Larry Luxner, senior correspondent for Rare Disease Advisor, interviews Patricia Weltin,founder and CEO of Beyond the Diagnosis—a nonprofit that uses art to raise public awareness of children with ultra-rare diseases.By Rare Care Podcast
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Transforming Photo Organization: Insights from Mylio's Founder David Vascovich
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Today, we have a special guest, David Vascovich, the CEO and founder of Mylio.com, a revolutionary digital photo organizing site. In this episode, we delve into the inspiration behind Mylio, its innovative features, and how it stands out in the crowded field of photo organization tools. Key Features of Mylio The Life Calendar: A unique way to visua…
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125: An Interview With Sarah Glass, PhD, of the n-Lorem Foundation
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Larry Luxner, senior correspondent for Rare Disease Advisor, interviews Sarah Glass, PhD, chief operating officer of the n-Lorem Foundation—and the mother of a boy with an ultra-rare disease.By Rare Care Podcast
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124: An Interview with Dimitrios Karussis, MD, PhD, on Stem Cell Therapy for Multiple Sclerosis
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Essential Genealogy Organization Tips: Listener Advice
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In this third solo podcast episode on organization and documentation, listeners shared tips to improve genealogy research. Weekly Paper Organization: Ann Marie recommends setting aside one hour each week, similar to Cindy Ingle’s “Filing Friday”. Note-taking Advice: Stress on thorough documentation to avoid forgetting crucial sources during intense…
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123: An Interview With Mary Morlino, Patient Navigator at the Undiagnosed Diseases Network Foundation
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Larry Luxner, senior correspondent for Rare Disease Advisor, interviews Mary Morlino, who has sarcoidosis and is the patient navigator for the Undiagnosed Diseases Network Foundation.By Rare Care Podcast
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Episode 97 - A Tale of Money, Crime, and Prison!
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22:58
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A discussion on genealogical research. A newspaper article leads to more information and intrigue in family history.By The Two Blondes
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Harnessing AI for Family Photo Tasks with Steve Little and Mark Thompson
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In this episode of "The Photo Detective," guests Steve Little and Mark Thompson return to discuss AI's integration in genealogy photo projects. They discuss historical breakthroughs in image analysis, such as the ability of AI to recognize visual jokes and extract text from images, such as tombstone inscriptions. They also cover the practical appli…
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122: An Interview WIth Tracy Sharp, a Patient With Lambert-Eaton Myasthenic Syndrome
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Navigating the New Era of AI in Genealogy with Steve Little and Mark Thompson
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In this episode of the Photo Detective Podcast, Maureen was joined by Mark Thompson, a professional genealogist and IT expert, and Steve Little, AI Program Director at the National Genealogical Society. Main Discussion Points: Comparisons of AI's current impact to the dot-com era. The role of small companies and startups in driving AI innovations. …
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121: An Interview With University of Pennsylvania Neurologist and CIDP Expert Chafic Karam, MD
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Unlocking Family Secrets: Expert Tips on Interviewing Relatives for Genealogy
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In today's solo episode, Maureen Taylor, the Photo Detective, delves into the essential practice of interviewing relatives for family history research. Following the feedback from newsletter subscribers and podcast listeners, this episode focuses on the collective wisdom and personal insights shared on this topic. We will explore the nuances of con…
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120: An Interview with Avner Reshef, MD, Top Israeli Expert in Hereditary Angioedema
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Larry Luxner, senior correspondent for Rare Disease Advisor, interviews Israeli expert Avner Reshef, MD, director of the Allergy, Immunology, and Angioedema Center at Barzilai University Medical Center in Ashkelon, only a few miles from the border with war-torn Gaza.By Rare Care Podcast
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119: An Interview With Pediatric Neurologist Edward Smith, MD, on the FDA Approval of Vamorolone for Boys With Duchenne Muscular Dystrophy
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Larry Luxner, senior correspondent for Rare Disease Advisor, interviews pediatric neurologist Edward Smith, MD, about the recent approval of vamorolone, a synthetic corticosteroid, in boys with Duchenne muscular dystrophy.By Rare Care Podcast
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118: An Interview With Sharon Hesterlee, PhD, Chief Research Officer at the Muscular Dystrophy Association
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Larry Luxner, senior correspondent for Rare Disease Advisor, interviews Sharon Hesterlee, PhD, chief research officer at the Muscular Dystrophy Association, about the recent proliferation of gene therapies and other treatments for neuromuscular diseases.By Rare Care Podcast
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Episode 96 -A Conversation with Maureen Taylor, the Photo Detective
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Discussion with Maureen Taylor, the Photo Detective, about using family photographs in genealogical research. Maureen Taylor discusses the secrets she uncovered in an old family photograph.By The Two Blondes
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Savoring the Story: Andrew Scravani on the Intersection of Food, Photography, and Life
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Today, we dive into the flavorful world of Andrew Scrivani, a renowned food photographer and author of “That Photo Makes Me Hungry”. Andrew shares his extensive experience spanning over two decades, revealing insights into the evolution of food photography, his creative process, and the broader implications of visual storytelling in our culinary ex…
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Digitize Your Past: How ScanMyPhotos.com Transformed Photo Preservation
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Mitch Goldstone, from ScanMyPhotos.com, returned to the Photo Detective Podcast to discuss the growth and evolution of his photo-scanning business. Having preserved over a billion pictures, the company specializes in digitizing old photographs, slides, and films, thus safeguarding personal and historical memories. Mitch shared the journey of adapti…
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117: An Interview With Ira Walker, the Muscular Dystrophy Association's 2024 National Ambassador, About Living With Spinal Muscular Atrophy
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Larry Luxner, senior correspondent for Rare Disease Advisor, interviews Ira Walker, the Muscular Dystrophy Association's 2024 National Ambassador, at the MDA's 2024 Clinical & Scientific Conference in Orlando, Florida. Walker, 39, has spinal muscular atrophy (SMA) type 2.By Rare Care Podcast
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116: An Interview With Seema Lalani, MD, Director of Project GIVE, a Pediatric Rare Disease Screening Program in the Rio Grande Valley of Texas
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Larry Luxner, senior correspondent for Rare Disease Advisor, interviews Seema Lalani, MD, of Baylor College of Medicine in Houston, Texas. Dr. Lalani directs Project GIVE (Genetic Inclusion by Virtual Evaluation), a pediatric screening program in the impoverished 4-county Rio Grande Valley region of southern Texas.…
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Tracing Your Roots: Key Strategies for New Genealogists
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In this solo episode, Maureen shares invaluable advice from her listeners, guiding beginner genealogists on their journey to trace their ancestry. From the critical importance of verification to the joy of discovering untold family stories, Maureen navigates through the collective wisdom of her audience, offering a treasure trove of tips and insigh…
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The Power of Relatives at RootsTech with Elizabeth Swanay O’Neal
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Elizabeth Swanay O’Neal discusses the popular Relatives at Rootstech feature, which allows conference registrants to connect with family. It’s free to sign up, easy to participate in, and only available until March 31, 2024. Elizabeth shares her strategies for using it. Register for RootsTech to access recorded content and participate in “Relatives…
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115: An Interview With Matt Trudeau of ITF Therapeutics, on Givinostat as a Therapy for Duchenne Muscular Dystrophy
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Larry Luxner, senior correspondent for Rare Disease Advisor, interviews Matt Trudeau, head of ITF Therapeutics—a division of Italy's Italfarmaco—on treating Duchenne muscular dystrophy with givinostat, a histone deacetylase inhibitor.By Rare Care Podcast
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