Hosted by Grey Genetics · 🇺🇸 US · EN · 94 episodes
Established thought leaders with verified media credentials.
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.
Grey Genetics hosts Patient Stories with Grey Genetics, a health show with 94 episodes published.
Nadia Billous is a mother of two young sons, including 9-year-old Andryusha who was diagnosed with GRIN2B-related neurodevelopmental disorder. Nadia and her family are Ukrainian and lived in Kyiv at the time of Andryusha
This episode was originally published in August 2018. Last Sunday, Sophie ran the London Marathon—her first of 36 marathons she plans to run in 36 days, as she raises money for Cystic Fibrosis Trust. You can follow Sophi
When Ushta was pregnant with her third child, she found herself being told which tests she would be having done—rather than being offered options and having them explained to her. As a genetic counselor working in reprod
Eleanor first interviewed Heather in 2018. At that time, Heather was several years out from completing a prophylactic mastectomy and oophorectomy related to her BRCA1 mutation and was living in Singapore. Her children we
As a teenager, Devin experienced what she now describes as mito crashes and thought it was just a normal part of being a teenager. Her older brother led the way to a shared diagnosis of an autosomal recessive mitochondri
Eleanor first interviewed Melanie in 2018. She was 29 years old at the time and had received a diagnosis of Lynch syndrome just before turning 25. Melanie shared her experience with receiving a diagnosis, recommended scr
This episode was originally published in February 2019. On June 24, 2024, Roe v. Wade was overturned. A few related links have been updated. Erika and Garin were 30 weeks into a complicated pregnancy when they learned
Dave and one of his younger sisters were both born with heart defects that required surgery. When Dave was 60, he was diagnosed with an aortic aneurysm. By this time, he had a daughter, Dawn Laney, who was a genetic coun
Eleanor first interviewed Abigail in 2019 when she was still a second year genetic counseling student. Abigail shared the story of her diagnosis of Wilson Disease and how it led her to a career in genetic counseling. She
Alexandra Parker is a senior student at Sarah Lawrence College. Alex describes her journey to a diagnosis of Hypermobile Ehlers-Danlos Syndrome and the skepticism that she faced from medical professionals. She had to adj
After losing her first son Alex at only 10 months of age to a rare genetic condition, Jill and her husband went on to have four more children. Jill’s youngest daughter, Katie, was always small from birth. By the time she
At 20 weeks of pregnancy, Jill learned that her son Alex had a diaphragmatic hernia. And a ventricular septal defect. An amniocentesis revealed a rare diagnosis of Mosaic Trisomy 5: some of her son’s cells had a typical
When Marleah was 8 years old, her mother was diagnosed with breast cancer. When Marleah was in college, her mother had genetic testing done and learned that she carried a mutation in the BRCA2 gene. This finding explaine
Molly sensed that something was different with her son Joshua starting shortly after birth: he was a very fussy baby; his growth was off the charts. By 10-12 months, Molly had the full attention of her pediatrician; Josh
Patient Stories is finally coming back with a new season. Do you want to share your story? Email us at podcast@greygenetics.com. You will be interviewed by Eleanor, a genetic counseling student, or..... you could also be
Patient Stories is taking a hiatus. We plan to be back in the fall with a third season. We would love to better understand our audience. If you could take 1 minute to fill out this survey, we would appreciate it! Check o
While Carlos was studying Biology in the U.S., his father was diagnosed with Philadelphia Chromosome positive Acute Lymphocytic Leukemia (Ph+ALL) in Mexico. The same condition which he’d just learned about in school and
A couple gets engaged. They are both of Ashkenazi Jewish ancestry and read that carrier testing is recommended. They rightly assume that the most likely outcome is that they will not be carriers for the same condition. T
When Layla was pregnant, she knew there was a 1 in 4 chance that her child would have Sickle Cell Disease. Routine newborn screening was done in London when Suki was 5 days old. She would be notified soon if her daughter
Munique had suffered from pain since she was 4 years old, but it wasn’t until she was 15 years old that she finally received a diagnosis that explained why: Fabry Disease. After seeing multiple doctors, she, her father,
Heather
VP of Content · Momentum: A Motorsports Podcast
1 appearance on this show
Devin
pediatric and family chiropractor · Cognition AI
1 appearance on this show
Melanie
teacher · How To Harp
1 appearance on this show
Abigail
student · Cheltenham Education Partnership
1 appearance on this show
Jill
tech safety expert · Postpartum Resource Center of New York
2 appearances on this show
Carlos
Head of Wine · JCP 360 bike fit
1 appearance on this show
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Patient Stories with Grey Genetics is hosted by Grey Genetics. The show is categorised under Health (Fitness) and has published 94 episodes.
Patient Stories with Grey Genetics has published 94 episodes.
Patient Stories with Grey Genetics regularly covers Health, Fitness, Medicine. It sits in the Health category, with a Fitness focus.
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Episodes of Patient Stories with Grey Genetics average 43 minutes. a focused format where a clear narrative arc and tight preparation matter most.
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