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AliveandKick'n the podcast

Robin Beth Dubin

AliveandKick'n the podcast

A weekly Health, Fitness and Kids podcast
Good podcast? Give it some love!
AliveandKick'n the podcast

Robin Beth Dubin

AliveandKick'n the podcast

Episodes
AliveandKick'n the podcast

Robin Beth Dubin

AliveandKick'n the podcast

A weekly Health, Fitness and Kids podcast
Good podcast? Give it some love!
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Episodes of AliveandKick'n the podcast

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I sit down with LeeAnne Hayden, Lynch Syndrome patient, ostomy patient, and host of The Beautiful Bag podcast.  Not only does she have an inspirational story, but she is also the first and only (so far) lynch syndrome podcaster that I've had on
I sit down with Alison Rosen, colon cancer survivor and lead on Project Echo for the American Cancer Society.  We talk about young adult survivorship, cancer advocacy and of course Lynch Syndrome. While Alison was 32 at diagnosis, she (so far)
Full disclosure, we recorded this in February, just as the Alabama Supreme Court IVF decision was handed down.  I sit down with Scott Weissman, Genetic Counselor and so much more, at the Norton & Elaine Sarnoff Center for Jewish Genetics.  Stat
I sit down with Dr Asaf Maoz, Medical Oncologist at Dana Farber Cancer Institute, who I recently saw at the LynkedIn and Scientific Symposium.  We discussed what brought Dr Maoz to this point, discussing immunology, T-cells, receptors and targe
I sit down with Emily Goldberg, Genetic Counselor for JScreen.  JScreen is a nonprofit that provides cancer genetics testing, but also has a reproductive carrier screening panel. Most patients choose saliva but sometimes blood is chosen by mobi
Boise Podcast pro Cody Mitchell joined me on the podcast as we talked Lynch Syndrome as she approaches her 4th cancerversary of endometrial cancer.  Cody has been able to turn her diagnosis into knowledge and cohesion among her network.  Cody i
I sit down with the Awkward Angler herself, Erica Nelson, from west of Denver in Crested Butte, Colorado.  Erica is a flyfishing guide in the Valley with a Lynch Syndrome story and so much more.  Erica also does consulting on diversity, equity
I sit down with Dianne Hammer, who shares her Lynch Syndrome story for the first time on a podcast.  Recently diagnosed, Diane is still a previvor, although she found pre-cancer when she had her hysterectomy.  She's also unsure which side of he
I sit down with Rachel Travis, otherwise known as the TattedRayofSunshine.  Not only does Rachel have a Lynch Syndrome colorectal and peritoneal cancer story, but also an alcohol, a firearms, a weight, a childhood trauma, rape and more.  Rachel
I sit down with Michelle Vina-Baltas, who has been having colonoscopies for 20 years, developed skin cancer 12 years ago, but only got tested for Lynch Syndrome recently.  Even as a life coach with tools for mitigating it, Michelle still gets a
I sit down with Amber Eastman, Lynch Syndrome survivor, and member of the Confederated Tribes of Ronde in Oregon. Amber confirmed with me that women of color face a more difficult challenge in that they are often noit believed, that they're cry
I sit down with Srinivas Pai, Lynch Syndrome survivor from lots of different places including India, Singapore, Michigan, New York and now Indiana.  While of course he has a rectal cancer story, how he and his wife, an Internist herself, manage
I sit down with Jaystan Davis, colon cancer survivor at age 19, as we discuss Lynch Syndrome, basketball, and more.  We also talk about how what was originally thought was an infection was actually additional cancers, so being your own advocate
I sit down with Dr Toni Seppala from Finland, GI surgeon, as we talk Lynch Syndrome and hockey instead of soccer for a change.  We talk risk-reducing surgeries, screening intervals, and the debate that continues, especially as it pertains to th
I sit down with Erin House, Lynch Syndrome survivor with a great story, including her running in the NYC marathon on behalf of AliveAndKickn.  Erin, originally from Australia, has an interesting story of genetics and international implications.
I sit down with Rachelle Manookian, Genetic Counselor at Children's Hospital of LA.  We discuss the transition from adult oncology at City of Hope to pediatrics, and the nuances it entails.  Rachelle and I originally met when she was a student
I talk with Dr Jose Perea Garcia, Digestive Surgeon as well as cancer researcher in Madrid.  We talk about how surgery has evolved and management of the Lynch Syndrome patient compared to sporadic cases.  We compare some protocols and coverage
I sit down with Dr Tiago Biachi, Medical Oncologist at Moffitt Cancer Center, as we discuss Lynch Syndrome, GI cancers, MSI, immunotherapy and of course soccer including the women's world cup, the pickup game at ASCO which I was not invited to,
I sit down with Dr William Karnes, Gastroenterologist and Director of High Risk and Colonoscopy Quality at the Digestive Health Institute at UC Irvine Health, as we discuss his accomplishments, including the launch of DocBot.  We discuss qualit
I talk community oncology with Dr Harsha Vyas, Oncologist at Cancer Center of Middle Georgia. Dr Vyas is also Advocacy Chair for the Community Oncology Alliance (COA). Belk, Kroger, and WalMart are the centers of the area, so people will come t
I had a conversation with Brian Kelly, life sciences and diagnostics professional.  Brian's career is expansive but working with pharma on advanced diagnostics has been his passion for the last dozen years.  Precision therapy is not a simple tr
I talk with Melissa Carr where we talk Lynch Syndrome, meteorology, and how she has dedicated herself to a number of public health initiatives in Wisconsin.  We also talk soccer and the Forward Madison (fla)mingos, her team Wildflowers team par
I sit down with Angela, psychotherapist in the UK and we talk Lynch Syndrome.  Angela went through her cancer journey during Covid, which has its own challenges.  We talk about coping with the mental and emotional strain and putting things into
I talk with Dr Marilena Mela and discuss her scientific evolution to where she is now.  Thankfully Dr Mela was exposed to Lynch Syndrome so much that she has focused on molecular genetics.  Dr Mela is PhD trained and is taking her board exams i
I talk with Shweta Walia, Lynch Syndrome patient from northern India.  Shweta has a significant history of cancer in her family, but she is the first to look into genetic testing and do something about it, both for herself and her daughter.  I
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