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MPN Forum Live is the only podcast designed exclusively for patients and caregivers of myeloproliferative neoplasms, also known as MPNs. MPNs include the following blood cancers, Polycythemia Vera, Essential Thrombocythemia and Myelofibrosis. MPN Forum Live brings together MPN patients from around the World to share their stories of living life as MPN patients. It’s the home to MPN patient storytelling. The MPN community is a band of brothers and sisters standing together; united to support each other while locked in the fight of their lives. You want to talk about failure not being an option? This is the very definition of failure not being an option. MPN Patients are not just warriors, they are also heroes who often struggle to find the mental fortitude to keep ongoing. Yet somehow, they find the strength to keep moving forward. From the dawn of time, human beings have shared a deep history of bonding with each other through the form of storytelling. MPN heroes all have fascinating and engaging stories to share. These stories provide MPN patients and their families with a unique experience not easily replicated on traditional social platforms. MPN Forum Live serves as an archival of stories for the families of MPN patients for download by family members and saved forever. Besides patient stories, from time to time, we will feature guest hosts, caregivers, hematologists and experts who can provide insight into medical breakthroughs and the benefits of exercise and a well-balanced diet.
9 Episodes
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Today’s guest is Dr. Hugh Young Rienhoff, Jr., a San Francisco Bay Area clinical physician-scientist and entrepreneur. He serves as the CEO and a Founder of Imago BioSciences, a clinical-stage biopharmaceutical company focused on developing novel therapeutics for patients with myeloproliferative neoplasms (MPNs), a family of related, chronic cancers of the bone marrow. In November 2022, Merck announced that it was acquiring Imago. They are using a differentiated pathway and mechanism of actio...
Today’s guest is Nikki. An ET MPN Patient who’s been kind enough to share her journey with the MPN Forum Live community. While many of us have the same MPN Nikki has her own unique experiences, trials and tribulations. Her story is inspiring and she shares many of her learnings. Hope you enjoy listening to her journey as much as I enjoyed interviewing her.
Today I had the pleasure of interviewing Krisstina Gowin Assistant Professor of Medicine at the University of Arizona for our MPN Forum Live Podcast. I heard her speak this year at the Hutch Center Seattle Patient Conference and she delivered an incredible presentation entitled "Living Well Amidst your Disease" which is about the new field of integrated oncology which provides a much more balanced form of treatment for MPN and Cancer Patients. We also spoke about how important exercise and di...
On todays podcast I am joined by Czerny Cohen VO of Clinical Operations for Massive Bio as well as Fiona Evans lead patient advocate for Massive BIO. You may have not heard of Massive Bio but you will be hearing a lot about them. They have created a service for MPN and Cancer patients that uses an AI-Powered technology which sorts through all available Clinical trials tailored specifically for your particular disease. You will not be shown Clinical Trials that you are not qualified for ...
On today’s podcast episode#5 of MPN Forum Live our guest is David Boule a former Navy man whose favorite movie is Top Gun. Who would have thought that? David was diagnosed with PV and is enjoying a very good life in the New Hampshire area where he golfs and enjoys like. As well as being an active member of the MPN Community he is also involved with raising money and supporting patient symposiums and other events.
Episode Description for the interview with Camille MJ to come...
What makes this interview with PV Patient Michael Goldstein interesting and different is that Michael is a Doctor. While there are many similarities between MPN Patient stories this story is different in particular because Michael is a Doctor and he sees thing differently. Michael is also a regular guy who happens to be from New York whose living his life with PV and trying to enjoy this grand journey called life. We take about Interferon, New York and Michael’s Family life. hope I hope you e...
Episode 1 MPN Forum Live Host Jeremy Smith takes you through some of his experiences as an MPN Patient for thirty-three years this year. From his first diagnosis and interaction with his very first first hematologist who told him he had at best ten years to live. To his 30 Years of working with Stanford Hematologist Stanley Schrier as well as his experiences with Dr. Ruben Mesa and Dr. Richard Silver and Jeremy’s fight to start using interferon. In addition Jeremy discusses why he founded MPN...
Jeremy Moberly was diagnosed with Polycythemia Vera in 2018 and is statistically on the younger end of the typical MPN Patient. We talk with Jeremy about his initial reaction to the diagnosis and how he has changed his life to live in this New World.We also talk about the importance of diet and exercise as well as how a thirty something MPN Patient deals with dating and sharing his situation with potential life partners.
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