Patient Stories with Grey Genetics
By Grey Genetics
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Subscribers: 16
Reviews: 0
Episodes: 93
Description
Genetics isn’t always black and white. And the emotions and decisions surrounding genetic testing can be even more complex. Hosted by genetic counselor Eleanor Griffith, the show brings you the personal experiences of patients and genetic counselors.
| Episode | Date |
|---|---|
|
Defying Cystic Fibrosis One Mountain at a Time [Rebroadcast]
|
Apr 23, 2024 |
|
Navigating Genetic Testing in Pregnancy & the Path to FiND Genetics
|
Apr 09, 2024 |
|
Next Chapter: Losing My Mother, Previving For My Children
|
Mar 26, 2024 |
|
Red Herrings, the Diagnostic Purgatory & Mitochondrial Disease
|
Mar 12, 2024 |
|
Next Chapter: Living with Lynch Syndrome
|
Feb 27, 2024 |
|
A Later Abortion Story
|
Feb 13, 2024 |
|
A Late Diagnosis of Cutis Laxa and the Creation of ThinkGenetics
|
Jan 30, 2024 |
|
Next Chapter: A Career in Genetic Counseling
|
Jan 16, 2024 |
|
Hypermobile Ehlers-Danlos Syndrome: An Invisible Condition
|
Jan 02, 2024 |
|
A Waiting Game & Another Diagnosis
|
Dec 12, 2023 |
|
Breaking Taboos & Leaving Room for Grief
|
Nov 28, 2023 |
|
Navigating the Uncertainty of a BRCA Mutation
|
Nov 14, 2023 |
|
Bardet-Biedl Syndrome and the Value of a Diagnosis
|
Oct 31, 2023 |
|
Coming Soon: Patient Stories, Season 3
|
Oct 24, 2023 |
|
Patient Stories is taking a hiatus…. Please take 1 minute to answer our survey!
|
Apr 13, 2021 |
|
Cancer, Genomics, and The Weight of Many Decisions
|
Mar 30, 2021 |
|
A Roll of the Dice
|
Mar 16, 2021 |
|
A Mother's Journey with Sickle Cell Disease
|
Mar 02, 2021 |
|
Far Away with Fabry
|
Feb 16, 2021 |
|
Epidermolysis Bullosa: Great Pain and Gigantic Love
|
Feb 02, 2021 |
|
The Loneliness of Living with Von Hippel-Lindau Syndrome
|
Jan 19, 2021 |
|
Changing the Narrative for Trisomy 18
|
Jan 05, 2021 |
|
Finding Support for Unexpected DNA Discoveries
|
Dec 22, 2020 |
|
A Long Diagnostic Odyssey to Ehlers-Danlos Syndrome
|
Dec 08, 2020 |
|
Pancreatic and GI Cancer Genetic Counseling
|
Nov 24, 2020 |
|
Finding Your Voice Through Dravet Syndrome
|
Nov 10, 2020 |
|
Family History 2.0
|
Oct 27, 2020 |
|
Psychiatric Genetic Counseling
|
Oct 13, 2020 |
|
Reaching New Heights with Hemophilia
|
Sep 29, 2020 |
|
Slowing Down with Mitochondrial Myopathy
|
Sep 15, 2020 |
|
Lucas & Menkes Disease: From Diagnosis Day to The Disorder Channel
|
Sep 01, 2020 |
|
Learning Compassion through Rett Syndrome
|
Aug 18, 2020 |
|
Not Parent Expected (NPE): The Untethering & My Own Story
|
Aug 04, 2020 |
|
Once Upon a Gene: "A Little Love"
|
Jul 29, 2020 |
|
Confronting Ageism with Lynch Syndrome
|
Jul 21, 2020 |
|
Androgen Insensitivity Syndrome (AIS): Finding Self-Acceptance and Connection
|
Jul 07, 2020 |
|
Representation Matters: Increasing Diversity within Genetic Counseling
|
Jun 20, 2020 |
|
Patient Stories is taking a hiatus…. Second Season to come in July!
|
Apr 02, 2020 |
|
Between Worlds: Usher syndrome type III
|
Mar 31, 2020 |
|
Talking about Prader-Willi syndrome with the host of Walking with Freya
|
Mar 17, 2020 |
|
Becoming BRCAStrong
|
Mar 03, 2020 |
|
Sandhoff Disease & A Spirit That Lives On
|
Feb 18, 2020 |
|
A Later Abortion Story
|
Feb 04, 2020 |
|
Walking with Freya: "Ep 53: Eleanor and Grey Genetics"
|
Jan 28, 2020 |
|
Unexpected Joys on the Scenic Route with Down Syndrome
|
Jan 21, 2020 |
|
Down Syndrome & Adoption as an Option
|
Jan 07, 2020 |
|
Patient Stories is taking a holiday break. More episodes in 2020!
|
Dec 24, 2019 |
|
She with Lynch
|
Dec 10, 2019 |
|
Family Health History and a Missed Diagnosis of Lynch Syndrome
|
Nov 26, 2019 |
|
Not Parent Expected (NPE): DNA, Identity, and Changing Family History
|
Nov 12, 2019 |
|
Beyond Survivorship: A Fresh Chapter
|
Oct 29, 2019 |
|
Losing, Living, and Laughing
|
Oct 15, 2019 |
|
Black and BRCA Positive
|
Oct 01, 2019 |
|
DNA Today, Episode #173: "Eleanor Griffith on Grey Genetics"
|
Sep 20, 2019 |
|
Resurrection Lily: A BRCA Memoir
|
Sep 17, 2019 |
|
A Short Life with Tay Sachs & Advocating for Preconceptual Carrier Screening
|
Sep 03, 2019 |
|
Can 23andMe Have It Both Ways?
|
Aug 27, 2019 |
|
Living a Full Life with SMA Type 2
|
Aug 20, 2019 |
|
A Window into Cri du Chat
|
Aug 06, 2019 |
|
Newborn Screening and Support for Glutaric Acidemia Type 1 (GA-1)
|
Jul 23, 2019 |
|
Fragile X: The Leading Genetic Cause of Autism
|
Jul 09, 2019 |
|
Wilson Disease: When early diagnosis makes all the difference
|
Jun 25, 2019 |
|
Men Get Breast Cancer Too!
|
Jun 11, 2019 |
|
“I have FH, FH doesn’t have me!”
|
May 28, 2019 |
|
Living and Learning with Huntington's
|
Apr 30, 2019 |
|
Gratitude After Gastrectomy
|
Apr 16, 2019 |
|
Fitness, Beauty, and Relationships in the BRCA World
|
Apr 02, 2019 |
|
Trisomies, Pregnancy Loss—And Options Counseling!
|
Mar 19, 2019 |
|
MUTYH, MAP, and Colorectal Cancer
|
Mar 05, 2019 |
|
Homocystinuria: A Rare Disease Often Missed on Newborn Screening
|
Feb 19, 2019 |
|
New in the Family: Ford and CTNNB1
|
Feb 05, 2019 |
|
Genetic Counseling: Past, Present and Future
|
Jan 22, 2019 |
|
Support Patient Stories!
|
Jan 17, 2019 |
|
To Gift or Not to Gift that At-Home DNA Testing Kit?
|
Dec 11, 2018 |
|
PKU: A Life-Giving Diagnosis
|
Nov 27, 2018 |
|
Surviving Pancreatic Cancer with the Help of Family, Faith, and Genetics
|
Nov 13, 2018 |
|
BRCA Positive and the Hard Choices that Follow
|
Oct 30, 2018 |
|
Living with and Beyond Early-Onset Breast Cancer
|
Oct 16, 2018 |
|
Building a Community of Hope and Support around Li-Fraumeni syndrome
|
Oct 09, 2018 |
|
Losing My Mother, Previving For My Children
|
Oct 02, 2018 |
|
Sickle Cell Disease: Invisible and Unpredictable
|
Sep 25, 2018 |
|
Ovarian Cancer, RAD51D, and Life Twice Over
|
Sep 11, 2018 |
|
Fighting for Sons with Duchenne
|
Aug 28, 2018 |
|
Defying Cystic Fibrosis One Mountain at a Time
|
Aug 14, 2018 |
|
Facing the World with Cleft Lip & Cleft Palate
|
Jul 31, 2018 |
|
New project coming
|
Jul 17, 2018 |
|
Growing in Empathy: Learning to Take My Own Advice and Seeing the Person Before the Patient
|
Jul 03, 2018 |
|
Genetic Counselors as Patient Advocates with Caroline Lieber
|
Jun 19, 2018 |
|
A Fatal Family Disease & the Flip of a Coin
|
Jun 05, 2018 |
|
Familial Hypercholesterolemia: The Symptomless Sickness
|
May 22, 2018 |
|
Making Sense of a Senseless Death
|
May 08, 2018 |
|
Living with Lynch syndrome - Melanie Breault
|
Apr 24, 2018 |
|
Patient Stories - Episode 0
|
Apr 13, 2018 |