최고 Lauren Freedman 팟캐스트 (2024)

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Last FREE Ep: The Thyroid Pharmacist! 46:29

10M ago46:29

46:29

Izabella Wentz, PharmD, FASCP, is an internationally acclaimed thyroid specialist and a licensed pharmacist who has dedicated her career to addressing the root causes of autoimmune thyroid disease after being diagnosed with Hashimoto’s thyroiditis in 2009. She is the author of three books on Hashimoto’s: Hashimoto’s Thyroiditis Lifestyle Interventi…

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Episode 149: BACK FROM HIBERNATION: NEW EPISODE 1:11:13

10M ago1:11:13

1:11:13

Chris Armstrong, PhD was first introduced to Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) through research into metabolomics at the University of Melbourne, Australia. As he delved deeper into his work, he discovered its connection to ME/CFS patients, and empathized so much with their plight – and the lack of resources, funding, and …

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148: Getting Sexy with Andrew Gurza 1:39:50

2y ago1:39:50

1:39:50

Andrew Gurza is an award winning Disability Awareness Consultant and the Chief Disability Officer and Co-founder of Bump’n, a sex toy company for and by disabled people. Andrew uses they/he pronouns and identifies proudly as disabled. Their work has been featured on BBC, CBC, Daily Xtra, Gay Times UK, Huffington Post, The Advocate, Everyday Feminis…

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147: Bipolar Señorita Dailyn Santana 1:00:13

2y ago1:00:13

1:00:13

Dailyn Santana is a first-generation Cuban-American actress, keynote speaker, spoken word poet, and mental health advocate. Her work focuses on eradicating mental health stigma and her personal experience of living with bipolar 1 disorder, depression, and anxiety. Her mission is to be an example that those living with mental illness CAN live a happ…

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146: SIBO Sisters and Hashi Posse Unite — It’s Phoebe Lapine! 57:47

2y ago57:47

57:47

Phoebe Lapine is a food and health writer, gluten-free chef, culinary instructor, recipe developer, wellness blogger, Hashimoto's advocate and speaker, and the voice behind the award-winning blog Feed Me Phoebe. Named by Women’s Health Magazine as the top nutrition read of 2017, Phoebe’s debut memoir, The Wellness Project, chronicles her journey wi…

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145: Crafted to Thrive: Mindset Business Coach & Spoonie Nikita Williams 1:20:14

2y ago1:20:14

1:20:14

Nikita Williams is a mindset business coach and the host of the podcast, She’s Crafted to Thrive. She was diagnosed with endometriosis in 2009 and fibromyalgia in 2010. These diagnoses inspired her to use the training she received from previous jobs to jump-start her career as a business coach. Nikita learned that having a chronic illness did not l…

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144: Endometriosis & Autism Advocate Kendall Rayburn 1:23:10

2y ago1:23:10

1:23:10

Originally launched as a means of sharing her craft projects, Kendall Rayburn’s namesake blog has since evolved into her passionate full-time occupation: a place to pour her heart into content across the lifestyle spectrum (see: plus-size fashion, family-friendly travel and activities, home decor, recipes, and more). It has also become a powerful v…

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143: Dr. Akilah Cadet, DEIB Specialist Living with Rare Heart Disease & hEDS 1:02:14

2+ y ago1:02:14

1:02:14

Dr. Akilah Cadet is the Founder and CEO of Change Cadet consulting firm, which offers a broad array of anti-racism and diversity services including strategic planning, crisis rebuilding, advising, executive coaching, and facilitation. Cadet (her last name) is a French term that means soldier. As it's often an uphill battle for BIPOC, women, and his…

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142: Racism Is A Public Health Crisis with Dr. Faith Crittenden 40:03

2+ y ago40:03

40:03

Faith Crittenden, MD MPH is a recently-graduated pediatric resident with her Doctorate of Medicine from the University of Connecticut School of Medicine. While a student, she was an active member of the Student National Medical Association (SNMA) and the American Medical Association (AMA). In 2016, she was appointed as the national liaison for SNMA…

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141: What We Really Mean When We Talk About OCD — With Pooja C. Danay 1:13:50

2+ y ago1:13:50

1:13:50

Pooja C. Danay is a South Asian mental health advocate who lives with obsessive-compulsive disorder (OCD). An actor, entrepreneur, and dancer who specializes in Bollywood dancing (been doing it since she was 5 years old!), she loves traveling and spending time with family and friends. Born and raised in New Jersey and currently living in NYC with h…

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140: Rare Diseases Lesotho Founder Nthabeleng Ramoeli 1:53:59

2+ y ago1:53:59

1:53:59

Nthabeleng Ramoeli was born in the small southern African country of Lesotho. At the age of 12, she began to experience chronic pain and subluxation of her joints, in addition to extreme skin elasticity, GI and lung issues, and anapyhlaxis. These symptoms persisted through her admittance to university, where test after test came back inconclusive. …

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139: The Boys of Bolus Maximus on Life with T1D 1:41:24

2+ y ago1:41:24

1:41:24

The idea behind non-profit community support organization Bolus Maximus began in late 2017 when Matt Tarro and Brandon A. Denson started having weekly discussions about their lives with type 1 diabetes (T1D). Coming from completely different backgrounds, the two actually had a lot in common — and recognized they both wanted to change the narrative …

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138: Morgan Greene — Is, Was, Will Be with MG 1:13:28

2+ y ago1:13:28

1:13:28

Morgan Greene is a chronic illness and holistic wellness blogger and content creator at Is Was Will Be blog. After being diagnosed with rare chronic illness Myasthenia Gravis (MG), Morgan started writing to process her experience — “serving as both therapy and accountability” for her, as she so aptly puts it. As her journey progressed, she found so…

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137: Lyfebulb Founder Dr. Karin Hehenberger 1:08:09

2+ y ago1:08:09

1:08:09

Dr. Karin Hehenberger has close to 20 years of experience in the life sciences sector. She served as an executive at Eyetech Pharmaceuticals and Coronado BioSciences, and had strategic management roles at Johnson & Johnson (Vice President, Metabolic Strategy), JDRF (Senior Vice President, Strategic Alliances), and McKinsey; as well as senior partne…

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136: When It Hurts to Hear — Hyperacusis Awareness Founder Jemma-Tiffany 1:02:57

2+ y ago1:02:57

1:02:57

Jemma-Tiffany is a 17-year-old writer, passionate patient advocate, and founder of Hyperacusis Awareness. Having grown up with severe hyperacusis (a rare and poorly-understood disorder that causes her to experience physical pain from everyday sounds) has motivated her to raise awareness of others with similar conditions. Through her various efforts…

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135: Defining Heroism: A 9/11 First Responder’s Story 1:46:14

2+ y ago1:46:14

1:46:14

* * * TW / CW : mortality, and graphic discussion of the events during and in the aftermath of 9/11, 2001 * * * Twenty years after 9/11, some first responders are still struggling with long-term health complications brought on by the historic event. For Tom Frey, a former NYC detective, the consequences started with a diagnosis of Hodgkin’s lymphom…

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134: Sara Naveed is Fabulous & Fatigued 1:20:46

2+ y ago1:20:46

1:20:46

Sara Naveed is a Canadian writer, chronic illness advocate, and founder of the blog Fabulous and Fatigued. 14 years ago, she was diagnosed with fibromyalgia following a hit-and-run. Inspired by her experience, she started the blog with the aim of creating awareness and ending the stigma of life with chronic illnesses. Her work has been published in…

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133: This Thing They Call Recovery’s Jenny McGibbon on The Nuanced Experience of Living with a Disability 1:16:10

2+ y ago1:16:10

1:16:10

Jenny McGibbon is a disabled graphic designer from Scotland, predominantly living with ME/CFS. She was born with a birth defect known as gastroschisis, and as a result she also lives with short bowel syndrome, chronic internal bleeding, and iron deficiency anemia. At the age of 16, she found herself in and out of hospital almost weekly — something …

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132: Lupus Advocate Cass Rush 1:14:57

2+ y ago1:14:57

1:14:57

Cassandra Rush is a lupus advocate born and raised in Los Angeles, CA. In 2012, after a two-year battle with an undiagnosed illness due to being uninsured, she was finally diagnosed with Systemic Lupus Erythematosus (lupus SLE). Two years later she was diagnosed with lupus nephritis. An “accidental advocate”, she speaks out about the broken US heal…

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131: Faith Ashenden of That Healing Feeling 57:54

2+ y ago57:54

57:54

Faith Ashenden is the founder and CEO of That Healing Feeling. She is a global patient empowerment mentor, master mindset coach, and biohacking expert who helps women hack the system and get their health back holistically, using 1-1 coaching, online courses, a podcast, and social media accounts with over 40k+ followers. Faith empowers people to ask…

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130: Actor & MS Advocate Damian Washington 54:53

3y ago54:53

54:53

Damian Washington is an actor who’s done 30+ commercials for brands like Fruit of the Loom, Realtor.com, and the NFL. Originally hailing from NYC, he attended the prestigious LaGuardia High School for the Performing Arts (Fame, anyone?!). A few years ago, he was diagnosed with multiple sclerosis (MS)…and soon discovered that developing an MS commun…

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129: ADHD Advocate Dani Donovan, Illustrator & Creator of #NeuroDiverseSquad 1:15:58

3y ago1:15:58

1:15:58

Dani Donovan is a purpose-driven designer who creates cathartic ADHD (attention-deficit/hyperactivity disorder) illustrations and a community of validation and solidarity for adults living with ADHD. Her first infographic, “ADHD Storytelling,” went viral within hours and amassed over 100 million views. Her work has been reposted by celebrities like…

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128: Diversability Founder Tiffany Yu 1:18:59

3y ago1:18:59

1:18:59

Tiffany Yu is the CEO & Founder of Diversability, an award-winning social enterprise to amplify disabled voices; the Founder of the Awesome Foundation Disability Chapter, a monthly micro-grant that has awarded $49.5k to 50 disability projects in 8 countries; and the host of TIFFANY & YU, the podcast. She serves on the San Francisco Mayor’s Disabili…

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127: Spoonie Artist & Activist Mimi Butlin of @CantGoOut_ImSick 1:09:54

3y ago1:09:54

1:09:54

In 2012, while studying at university, Mimi Butlin contracted viral meningitis — from which she never fully recovered. Since then she has been diagnosed with Ehlers-Danlos syndrome, fibromyalgia, postural orthostatic tachycardia syndrome, and ME/CFS (as Mimi wryly notes, “a really lovely bunch!”). For years, she felt completely alone and that convi…

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126: The Mata Sisters, Founders of Looms for Lupus 1:23:00

3y ago1:23:00

1:23:00

In 2009, Juana Mata was diagnosed with lupus. One of three very close sisters, nobody in her family had heard of this illness prior to her diagnosis — or knew how to handle her support and treatment. As the family began to research education, resources, and the history of the disease, they began to discover that it was largely misunderstood, and th…

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125: Fight Like A Warrior Founder Alexa Chronister 41:33

3y ago41:33

41:33

Alexa Chronister is the founder and president of Fight Like A Warrior (FLAW). She created FLAW after creating the Cards For Warriors program (sending handmade cards of encouragement to chronic illness warriors across the globe, reminding them they are not alone) in 2016. With the goal of creating a community of empowerment and improving the lives o…

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124: Julian Gavino, @TheDisabledHippie 1:02:12

3y ago1:02:12

1:02:12

Julian Gavino (he/him) is a trans-masculine model, writer, coach, and sex-positive disability influencer living with Ehlers-Danlos syndrome and comorbidities. An outspoken advocate for both the trans and disability communities, Julian grew up never seeing people in media who “looked like” him…and his work has become a direct response to that experi…

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123: Don’t Judge A Book By Its Cover: Shayla Swint on Life with EDS 47:21

3y ago47:21

47:21

Shayla Swint is a 25-year-old college grad from Houston, Texas. Like the old adage, “Don’t judge a book by its cover,” Shayla is so much more than what we can see…she lives with connective tissue disorder Ehlers-Danlos Syndrome (EDS), hypermobile type. She’s survived over 15 surgeries thus far, and lives in an almost-constant state of pain and anxi…

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122: Rhisa Parera: A WOC VS The System — And Lyme 1:26:13

3y ago1:26:13

1:26:13

In the last in our 2021 series on Lyme disease, we are joined by the first WOC to discuss the subject: Rhisa Marie Parera. Though she began experiencing symptoms from a young age, Rhisa grew up as an active young woman in Staten Island, NY, and got heavily involved in the salsa dancing scene and modeling from her late teens into her early twenties.…

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121: Functional Medicine Health Coach Sharon Leggio Falchuk VS Lyme 1:34:51

3y ago1:34:51

1:34:51

Sharon Leggio Falchuk, FMCHC found herself bedridden by a serious illness in 2011, and when the mainstream medical system had no answers or help for her she took matters into her own hands. She spent every moment she could doing research, changing her diet and lifestyle, and assembling a functional medicine and alternative care team to help her for…

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120: Lyme & Thyroid Specialist Lisa Hunt, D.O. 32:25

3y ago32:25

32:25

Lisa Hunt, D.O., D.O.H. is a practitioner at Holtorf Medical Group in El Segundo, CA. She specializes in anti-aging treatment, natural thyroid replacement, menopause/andropause therapy (including bioidentical hormone replacement), chronic fatigue syndrome, fibromyalgia, strengthening the immune system, neurotransmitter analysis/replacement, and nut…

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119: Buenqamino, Lyme & Co. 1:01:31

3y ago1:01:31

1:01:31

Christina Kantzavelos (@buenqamino // @beginwithintoday) is a Lyme warrior, award-winning freelance writer/content creator, chronic illness advocate, and licensed psychotherapist. She was diagnosed with Lyme disease and co-infections in October of 2018. However, she struggled with debilitating symptoms and various autoimmune diseases for years prio…

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118: LLMD Dr. Casey Kelley 50:07

3y ago50:07

50:07

Casey Kelley, MD, ABoIM is the founder and medical director of Case Integrative Health. Dr. Kelley is relentless about getting to the root cause of chronic disease and transforming health through Functional Medicine. On faculty at Northwestern's Feinberg School of Medicine, she is Board Certified in Family Medicine and was also among the first phys…

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117: Alex Moresco, Lyme Advocate & Co-Founder of Advocacy Express 1:02:48

3y ago1:02:48

1:02:48

Whether it’s hiding the likes of Pamela Anderson from paparazzi or helping NeNe Leakes pretend to sell furniture…Alex Moresco has a story about it. A PR executive from Chicago, four years ago her life was turned upside-down by undiagnosed illness. It took her two years and eight specialists (a shorter time than most, she admits) to find a doctor th…

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116: Lyme Survivor & Life Sherpa Gena Chieco 38:21

3y ago38:21

38:21

Gena Chieco is a coach, adventurer, and connector who loves inspiring clients to step into their best lives by providing tools to help them tap into their inner wisdom and dreams. She grew up in a rural suburb of New York City running around barefoot in the summer, obsessed with nature, with dreams of becoming a zoologist. After earning a BA with H…

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115: Integrative Rheumatologist Dr. Micah Yu 50:27

3y ago50:27

50:27

Dr. Micah Yu is an integrative rheumatologist who incorporates complementary medicine with traditional rheumatology. He is double board-certified in internal medicine and lifestyle medicine. He obtained his MD from Chicago Medical School, and holds a Masters in Healthcare Administration and Biomedical sciences. He completed his internal medicine re…

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114: Black Disabled Artist Rana 2.0 53:41

3y ago53:41

53:41

Artist Rana Awadallah grew up surrounded by poverty, abuse, and trauma. Diagnosed with major depression and extreme anxiety at the age of 18, she always felt there was something “wrong” with her body. Then, at the age of 24 — after having dealt with chronic pain for a decade — she was diagnosed with osteoarthritis in both of her knees. Shortly afte…

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113: Myositis Thriver Michole J 58:52

3y ago58:52

58:52

Michole J lives with rare muscle disease polymyositis (PM), which falls under the umbrella of muscular dystrophy. PM is an uncommon inflammatory disease that affects the entire body — and while Michole began to exhibit symptoms in her late 20s, she was diagnosed at age 30 with the rarest form. Living with the condition create mobility challenges, f…

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112: Somatic & Spoonie Therapist Rachel Otis Lives with Crohn’s Disease 1:29:52

3y ago1:29:52

1:29:52

Rachel Otis (she/they) is a somatic therapist, yoga teacher, abolitionist, writer, and pleasure activist who works directly, compassionately and non-judgmentally with the mind-body connection, infusing sessions, groups, retreats, and articles with radical self-love, exploration, and expression. She provides healing pathways of somatically-oriented …

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111: P4AD’s Samantha Reid on Patient Advocacy & Life with Crohn’s Disease 1:24:40

3+ y ago1:24:40

1:24:40

Samantha Reid is the Digital Director for Patients for Affordable Drugs. Growing up in Illinois, she suffered from a “bad stomach” and weakened immune system, having caught pneumonia nine times by the age of nine. But it wasn’t until she was in her late teens that she sought answers. A diagnosis of Crohn’s disease eventually led her into patient ad…

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110: P4AD’s David Mitchell on Drug Pricing and Living with Incurable Cancer 1:06:28

3+ y ago1:06:28

1:06:28

David Mitchell has an incurable blood cancer called multiple myeloma. The price of his current drugs is more than $875,000 per year. Like millions of Americans, David needs innovation and new drugs to survive, but he believes drugs don’t work if people can’t afford them. After more than 30 years at a D.C. policy and communications firm, he retired …

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109: Breath, Movement, and Chronic Pain with TN Advocate Kayla Harley 1:08:12

3+ y ago1:08:12

1:08:12

Kayla Harley is a certified GYROKINESISⓇ instructor, Optimal Life Breath Pathologist, doula, and energy healer helping dancers, athletes and everyday movers alike improve their quality of movement: for breath integration and to prevent injury. She is an International Practitioner and among the forerunners in the International Association for Blacks…

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108: New Series! Innovators — Part 1 1:15:21

3+ y ago1:15:21

1:15:21

Join us as we launch a brand new series on Uninvisible Pod — INNOVATORS! In this series, we will periodically release episodes including short-form interviews with founders whose work is creating waves of change in chronic and invisible illness and disability. First up, as we dive in to the end of the year and look forward into 2021: Yale graduate …

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107: The Point of Pain with Chronicon Founder Nitika Chopra 51:42

3+ y ago51:42

51:42

At the age of 10, Nitika Chopra was diagnosed with a debilitating case of psoriasis. By 19, her joints were entirely inflamed and she was further diagnosed with psoriatic arthritis. From the tips of her toes to the crown of her head, her body was covered in unsightly sores…and for the first five years of her second diagnosis, she was unable to move…

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106: That Chronic Pain Life with The Migraine Diva Jaime Sanders 1:04:02

3+ y ago1:04:02

1:04:02

Jaime Sanders’ journey with migraine has been life-long. From a toddler with abdominal migraine to a wife and mother with chronic intractable migraine, Jaime has learned to turn her pain into empowerment. She also manages her daily life with depression and anxiety, surviving two suicide attempts, along with fibromyalgia, carpal tunnel syndrome, spi…

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105: Naturalist Brittany Sumner on Living with Rare Disease Paramyotonia Congenita 1:02:39

3+ y ago1:02:39

1:02:39

Born and raised in South Carolina, 27-year-old Brittany Sumner always felt like she was different than her peers — both physically and mentally. At an early age, she began falling over without explanation, finding herself unable to climb stairs, going cross-eyed, experiencing slurred speech, choking on food, and feeling almost constant fatigue. It …

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104: Special Needs Siblings Founder Jeniece Dortch 1:08:56

3+ y ago1:08:56

1:08:56

Jeniece Dortch is a mom of six, her children ranging in age from 4-16 years. She has a passion for the special needs community that was born when her second-eldest son, Christian Garcia, was diagnosed with autism and epilepsy. She not only saw the need to advocate for these communities, but for the entire family unit (even those who are able-bodied…

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103: Advocating Like A Mother: Kelly Cervantes on Life After Epilepsy 52:37

3+ y ago52:37

52:37

In May 2016, Kelly Cervantes and her family received two life-changing pieces of news: her husband, Miguel, had landed the starring role of Alexander Hamilton in Hamilton: An American Musical in Chicago; and their then-7-months-old baby girl, Adelaide, was diagnosed with epilepsy — and eventually, infantile spasms — a severe form of childhood epile…

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102: Angels of Epilepsy Founder Natalie Y. Beavers 42:46

3+ y ago42:46

42:46

Natalie Y. Beavers is an award-winning epilepsy survivor, advocate, and founder of the Angels Of Epilepsy Foundation, a non-profit organization that brings awareness, education, and community to epilepsy survivors and their families nationwide. Diagnosed with epilepsy at the age of 5, a seizure while she was driving in 2006 caused a life-changing a…

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101: Breast Cancer Survivor Vatesha Bouler 50:21

3+ y ago50:21

50:21

An educator for over 20 years, Vatesha Bouler is a kindergarten teacher and (almost!) six-year breast cancer survivor. Diagnosed at a relatively young age, her experience pushed her to believe that life must be lived to the fullest — and she walks that walk every day in her advocacy work for others enduring similar experiences. A public speaker and…

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