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Navigating the Uncertainty of a BRCA Mutation
Manage episode 383742476 series 3051496
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 explained the breast cancer in Marleah’s family and inspired Marleah’s career as a university professor, focused on communication and decision making surrounding hereditary cancer risk. Marleah met with a genetic counselor when she was in her PhD program but chose to wait until she was 25 before she had genetic testing done and learned that she also carried a BRCA2 mutation. Marleah shares her own journey as a previvor and discusses her ongoing work in the field.
Links and Resources
Marleah’s Tedx Talk: How to Make Decisions Based on Uncertain Information
Marleah as part of the CDC’s Bring Your Brave Campaign
Marleah’s campaign video for the CDC
Dean M, et al. “Shared Decision-Making Experiences of Couples with Inherited Cancer Risk Regarding Family Building.” J Health Commun. 2023 May 4;28(5):292-301.
https://www.facingourrisk.org/BOAST/
Facing Our Risk of Cancer Empowered
Connect with Marleah on Social Media
Marleah on Twitter @marleahdeank
Check out other Patient Stories podcast episodes.
Read other Patient Stories on the Grey Genetics Patient Stories Page.
Interested in digging deeper into the professional issues raised in the podcast? Consider joining the Patient Stories Club!
Do you want to support Patient Stories? You can make a donation online!
Are you looking for genetic counseling? Patient Stories is sponsored by Grey Genetics, an independent telehealth genetic counseling and consulting company. Book an appointment with a genetic counselor specialized in your area of concern. All genetic counseling appointments take place over secure, HIPAA-compliant video-conferencing or by phone.
Looking for a place to collect your family history and share with relatives? Check out the FamGenix app.
Grey Genetics is no longer active on social media. To receive occasional email updates, sign up for our mailing list.
94 episoade
Manage episode 383742476 series 3051496
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 explained the breast cancer in Marleah’s family and inspired Marleah’s career as a university professor, focused on communication and decision making surrounding hereditary cancer risk. Marleah met with a genetic counselor when she was in her PhD program but chose to wait until she was 25 before she had genetic testing done and learned that she also carried a BRCA2 mutation. Marleah shares her own journey as a previvor and discusses her ongoing work in the field.
Links and Resources
Marleah’s Tedx Talk: How to Make Decisions Based on Uncertain Information
Marleah as part of the CDC’s Bring Your Brave Campaign
Marleah’s campaign video for the CDC
Dean M, et al. “Shared Decision-Making Experiences of Couples with Inherited Cancer Risk Regarding Family Building.” J Health Commun. 2023 May 4;28(5):292-301.
https://www.facingourrisk.org/BOAST/
Facing Our Risk of Cancer Empowered
Connect with Marleah on Social Media
Marleah on Twitter @marleahdeank
Check out other Patient Stories podcast episodes.
Read other Patient Stories on the Grey Genetics Patient Stories Page.
Interested in digging deeper into the professional issues raised in the podcast? Consider joining the Patient Stories Club!
Do you want to support Patient Stories? You can make a donation online!
Are you looking for genetic counseling? Patient Stories is sponsored by Grey Genetics, an independent telehealth genetic counseling and consulting company. Book an appointment with a genetic counselor specialized in your area of concern. All genetic counseling appointments take place over secure, HIPAA-compliant video-conferencing or by phone.
Looking for a place to collect your family history and share with relatives? Check out the FamGenix app.
Grey Genetics is no longer active on social media. To receive occasional email updates, sign up for our mailing list.
94 episoade
Toate episoadele
×1 GRIN2B: An Odyssey from Diagnosis to Evacuation 29:43
1 Defying Cystic Fibrosis One Mountain at a Time [Rebroadcast] 36:15
1 Navigating Genetic Testing in Pregnancy & the Path to FiND Genetics 52:02
1 Next Chapter: Losing My Mother, Previving For My Children 55:58
1 Red Herrings, the Diagnostic Purgatory & Mitochondrial Disease 1:12:28
1 Next Chapter: Living with Lynch Syndrome 46:47
1 A Later Abortion Story 1:31:26
1 A Late Diagnosis of Cutis Laxa and the Creation of ThinkGenetics 38:07
1 Next Chapter: A Career in Genetic Counseling 20:20
1 Hypermobile Ehlers-Danlos Syndrome: An Invisible Condition 25:50
1 A Waiting Game & Another Diagnosis 1:08:54
1 Breaking Taboos & Leaving Room for Grief 1:11:01
1 Navigating the Uncertainty of a BRCA Mutation 38:39
1 Bardet-Biedl Syndrome and the Value of a Diagnosis 42:37
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