Patient Stories with Grey Genetics

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Patient Stories with Grey Genetics

Navigating Genetic Testing in Pregnancy & the Path to FiND Genetics

When Ushta was pregnant with her third child, she found herself being told which tests she would...

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Next Chapter: Losing My Mother, Previving For My Children

Eleanor first interviewed Heather in 2018. At that time, Heather was several years out from...

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The Diagnostic Purgatory of Mitochondrial Disease

As a teenager, Devin experienced what she now describes as mito crashes and thought it was just a...

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Next Chapter: Living with Lynch Syndrome

Eleanor first interviewed Melanie in 2018. She was 29 years old at the time and had received a...

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A Later Abortion Story

This episode was originally published in February 2019. On June 24, 2024, ⁠Roe v. Wade was...

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A Late Diagnosis of Cutis Laxa and the Creation of ThinkGenetics

Show Notes Dave and one of his younger sisters were both born with heart defects that required...

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Next Chapter : A Career in Genetic Counseling

Eleanor first interviewed Abigail in 2019 when she was still a second year genetic counseling...

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Hypermobile Ehlers-Danlos Syndrome: An Invisible Condition

Alexandra Parker is a senior student at Sarah Lawrence College. Alex describes her journey to a...

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A Waiting Game & Another Diagnosis

After losing her first son Alex at only 10 months of age to a rare genetic condition, Jill and...

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Breaking Taboos & Leaving Room for Grief

At 20 weeks of pregnancy, Jill learned that her son Alex had a diaphragmatic hernia. And a...

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Navigating the Uncertainty of a BRCA2 mutation

When Marleah was 8 years old, her mother was diagnosed with breast cancer. When Marleah was in...

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Bardet-Biedl Syndrome and the Value of a Diagnosis

Molly sensed that something was different with her son Joshua starting shortly after birth: he...

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Coming Soon: Patient Stories, Season 3

Patient Stories is finally coming back with a new season. Do you want to share your story?...

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Patient Stories is taking a hiatus…. Please take 1 minute to answer our survey!

Patient Stories is taking a hiatus. We plan to be back in the fall with a third season. We would...

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Cancer, Genomics, and The Weight of Many Decisions

While Carlos was studying Biology in the U.S., his father was diagnosed with Philadelphia...

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A Roll of the Dice

A couple gets engaged. They are both of Ashkenazi Jewish ancestry and read that carrier testing...

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A Mother's Journey with Sickle Cell Disease

When Layla was pregnant, she knew there was a 1 in 4 chance that her child would have Sickle Cell...

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Far Away with Fabry

Munique had suffered from pain since she was 4 years old, but it wasn’t until she was 15 years...

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Epidermolysis Bullosa: Great Pain and Gigantic Love

Silvia’s son Nicky was born with a devastating condition called Epidermolysis Bullosa (EB). On...

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The Loneliness of Living with Von Hippel-Lindau Syndrome

As a junior in high school, Mikaela played varsity softball. When her performance started to...

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