Patient Stories with Grey Genetics

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

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