All Episodes
Patient Stories with Grey Genetics — 94 episodes
GRIN2B: An Odyssey from Diagnosis to Evacuation
Defying Cystic Fibrosis One Mountain at a Time [Rebroadcast]
Navigating Genetic Testing in Pregnancy & the Path to FiND Genetics
Next Chapter: Losing My Mother, Previving For My Children
Red Herrings, the Diagnostic Purgatory & Mitochondrial Disease
Next Chapter: Living with Lynch Syndrome
A Later Abortion Story
A Late Diagnosis of Cutis Laxa and the Creation of ThinkGenetics
Next Chapter: A Career in Genetic Counseling
Hypermobile Ehlers-Danlos Syndrome: An Invisible Condition
A Waiting Game & Another Diagnosis
Breaking Taboos & Leaving Room for Grief
Navigating the Uncertainty of a BRCA Mutation
Bardet-Biedl Syndrome and the Value of a Diagnosis
Coming Soon: Patient Stories, Season 3
Patient Stories is taking a hiatus…. Please take 1 minute to answer our survey!
Cancer, Genomics, and The Weight of Many Decisions
A Roll of the Dice
A Mother's Journey with Sickle Cell Disease
Far Away with Fabry
Epidermolysis Bullosa: Great Pain and Gigantic Love
The Loneliness of Living with Von Hippel-Lindau Syndrome
Changing the Narrative for Trisomy 18
Finding Support for Unexpected DNA Discoveries
A Long Diagnostic Odyssey to Ehlers-Danlos Syndrome
Pancreatic and GI Cancer Genetic Counseling
Finding Your Voice Through Dravet Syndrome
Family History 2.0
Psychiatric Genetic Counseling
Reaching New Heights with Hemophilia
Slowing Down with Mitochondrial Myopathy
Lucas & Menkes Disease: From Diagnosis Day to The Disorder Channel
Learning Compassion through Rett Syndrome
Not Parent Expected (NPE): The Untethering & My Own Story
Once Upon a Gene: "A Little Love"
Confronting Ageism with Lynch Syndrome
Androgen Insensitivity Syndrome (AIS): Finding Self-Acceptance and Connection
Representation Matters: Increasing Diversity within Genetic Counseling
Patient Stories is taking a hiatus…. Second Season to come in July!
Between Worlds: Usher syndrome type III
Talking about Prader-Willi syndrome with the host of Walking with Freya
Becoming BRCAStrong
Sandhoff Disease & A Spirit That Lives On
A Later Abortion Story
Walking with Freya: "Ep 53: Eleanor and Grey Genetics"
Unexpected Joys on the Scenic Route with Down Syndrome
Down Syndrome & Adoption as an Option
Patient Stories is taking a holiday break. More episodes in 2020!
She with Lynch
Family Health History and a Missed Diagnosis of Lynch Syndrome
Not Parent Expected (NPE): DNA, Identity, and Changing Family History
Beyond Survivorship: A Fresh Chapter
Losing, Living, and Laughing
Black and BRCA Positive
DNA Today, Episode #173: "Eleanor Griffith on Grey Genetics"
Resurrection Lily: A BRCA Memoir
A Short Life with Tay Sachs & Advocating for Preconceptual Carrier Screening
Can 23andMe Have It Both Ways?
Living a Full Life with SMA Type 2
A Window into Cri du Chat
Newborn Screening and Support for Glutaric Acidemia Type 1 (GA-1)
Fragile X: The Leading Genetic Cause of Autism
Wilson Disease: When early diagnosis makes all the difference
Men Get Breast Cancer Too!
“I have FH, FH doesn’t have me!”
Living and Learning with Huntington's
Gratitude After Gastrectomy
Fitness, Beauty, and Relationships in the BRCA World
Trisomies, Pregnancy Loss—And Options Counseling!
MUTYH, MAP, and Colorectal Cancer
Homocystinuria: A Rare Disease Often Missed on Newborn Screening
New in the Family: Ford and CTNNB1
Genetic Counseling: Past, Present and Future
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To Gift or Not to Gift that At-Home DNA Testing Kit?
PKU: A Life-Giving Diagnosis
Surviving Pancreatic Cancer with the Help of Family, Faith, and Genetics
BRCA Positive and the Hard Choices that Follow
Living with and Beyond Early-Onset Breast Cancer
Building a Community of Hope and Support around Li-Fraumeni syndrome
Losing My Mother, Previving For My Children
Sickle Cell Disease: Invisible and Unpredictable
Ovarian Cancer, RAD51D, and Life Twice Over
Fighting for Sons with Duchenne
Defying Cystic Fibrosis One Mountain at a Time
Facing the World with Cleft Lip & Cleft Palate
New project coming
Growing in Empathy: Learning to Take My Own Advice and Seeing the Person Before the Patient
Genetic Counselors as Patient Advocates with Caroline Lieber
A Fatal Family Disease & the Flip of a Coin
Familial Hypercholesterolemia: The Symptomless Sickness
Making Sense of a Senseless Death
Living with Lynch syndrome - Melanie Breault
Patient Stories - Episode 0