I'm Aware That I'm Rare: the phaware® podcast
987 episodes - English - Latest episode: 13 days ago - ★★★★★ - 14 ratingsI'm Aware That I'm Rare: the phaware® podcast is devoted to raising global pulmonary hypertension awareness with dynamic stories from PH patients, caregivers and medical professionals from around the world.
Through this series of impactful, insightful and, most importantly, hopeful stories from members of the global pulmonary hypertension community, we hope to further the global #phaware conversation as well as to capture, engage and enable misdiagnosed and undiagnosed PH patients because early diagnosis and treatment can mean the difference between life and death.
Topics range from the importance of early diagnosis and global PH awareness, to the impact of clinical trials to how patient support and advocacy are paramount to battling this disease.
Learn more about PH at www.phaware.global
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Episodes
Sanjay Mehta, MD - phaware® interview 212
January 15, 2019 13:00Sanjay Mehta, MD, FRCPC, FCCP, is PHA Canada’s Chair. He is additionally Professor of Medicine at the University of Western Ontario, and Director of the Southwest Ontario Pulmonary Hypertension Clinic at the London Health Sciences Center in London, Canada. He is also Chair of the Pulmonary Vascular Disease Committee of the Canadian Thoracic Society. Dr. Mehta has been caring for patients with PH and doing research in PH since 1989. In this episode, Dr. Mehta discusses the importance of earl...
Episode 212 - Sanjay Mehta, MD
January 14, 2019 13:00 - 7 minutes - 6.81 MBSanjay Mehta, MD, FRCPC, FCCP, is PHA Canada’s Chair. He is additionally Professor of Medicine at the University of Western Ontario, and Director of the Southwest Ontario Pulmonary Hypertension Clinic at the London Health Sciences Center in London, Canada. He is also Chair of the Pulmonary Vascular Disease Committee of the Canadian Thoracic Society. Dr. Mehta has been caring for patients with PH and doing research in PH since 1989. In this episode, Dr. Mehta discusses the importance of early...
Lori Heaton - phaware® interview 211
November 30, 2018 13:00Pulmonary hypertension caregiver and author, Lori Heaton discusses her daughter Maddie's twenty-year journey of courage and strength living with PH. Maddie conquered cancer and lived on to receive two separate lung transplants. Lori details wisdom learned being Maddie’s caregiver through hard-gained lessons which she calls "difficult blessings." My name is Lori Heaton. I was a parent caregiver to my daughter Madison Heaton. We are from Provo, Utah. Maddie was diagnosed with pulmonary hype...
Episode 211 - Lori Heaton
November 29, 2018 13:00 - 13 minutes - 14.3 MBPulmonary hypertension caregiver and author, Lori Heaton discusses her daughter Maddie's twenty-year journey of courage and strength living with PH. Maddie conquered cancer and lived on to receive two separate lung transplants. Lori details wisdom learned being Maddie’s caregiver through hard-gained lessons which she calls "difficult blessings." Learn more about pulmonary hypertension trials at www.phaware.global/clinicaltrials. Never miss an episode with the phaware® podcast app. Follow u...
Kristine Ritchie - phaware® interview 210
November 27, 2018 13:00Pediatric PH caregiver Kristine Ritchie discusses her son Brendan’s pulmonary hypertension diagnosis. Kristine talks about the importance of advocating for her child, the power of online support groups and struggle of navigating a new normal. My name is Kristine Ritchie, I am from the Central Interior of BC in West Kelowna. I am the parent of an idiopathic pulmonary hypertension child who is 10 years old, and he was diagnosed at four and a half years old on December 12th of 2012. Brend...
Episode 210 - Kristine Ritchie
November 26, 2018 13:00 - 6 minutes - 8.22 MBPediatric PH caregiver Kristine Ritchie discusses her son Brendan’s pulmonary hypertension diagnosis. Kristine talks about the importance of advocating for her child, the power of online support groups and struggle of navigating a new normal. Learn more about pulmonary hypertension trials at www.phaware.global/clinicaltrials. Never miss an episode with the phaware® podcast app. Follow us @phaware on Facebook, Twitter, Instagram, YouTube & Linkedin Engage for a cure: www.phaware.global/don...
Sonya Collins - phaware® interview 209
November 23, 2018 13:00Diagnosed with IPAH almost 16 years ago, Canadian Sonya Collins discusses spending about four years questioning her shortness of breath (SOB) and severe fluid retention. Sonya details why she became a PHA Canada Ambassador and how her short and long term goals have shifted over the years thanks to her PH therapies. My name is Sonya Collins, and I'm from Paradise Newfoundland, Canada. I am a PH patient. I have been diagnosed for almost 16 years and have recently become an ambassador for PH...
Episode 209 - Sonya Collins
November 22, 2018 13:00 - 8 minutes - 9.35 MBDiagnosed with IPAH almost 16 years ago, Canadian Sonya Collins discusses spending about four years questioning her shortness of breath (SOB) and severe fluid retention. Sonya details why she became a PHA Canada Ambassador and how her short and long term goals have shifted over the years thanks to her PH therapies. Learn more about pulmonary hypertension trials at www.phaware.global/clinicaltrials. Never miss an episode with the phaware® podcast app. Follow us @phaware on Facebook, Twitter...
Shannon Reitor - phaware® interview 208
November 20, 2018 13:00Pediatric PH caregiver Shannon Reitor discusses her son Adam’s pulmonary hypertension diagnosis. Shannon details lobbying the Canadian government, the challenge of navigating side-effects of unapproved treatments for children with PH and how Adam became the first child in Canada to go on IV therapy. My name is Shannon Reitor. I am from Edmonton, Alberta, in Canada, and my connection to pulmonary hypertension is through my son, Adam. He was diagnosed the day before his second birthday. I...
Episode 208 - Shannon Reitor
November 19, 2018 13:00 - 4 minutes - 4.44 MBPediatric PH caregiver Shannon Reitor discusses her son Adam’s pulmonary hypertension diagnosis. Shannon details lobbying the Canadian government, the challenge of navigating side-effects of unapproved treatments for children with PH and how Adam became the first child in Canada to go on IV therapy. Learn more about pulmonary hypertension trials at www.phaware.global/clinicaltrials. Never miss an episode with the phaware® podcast app. Follow us @phaware on Facebook, Twitter, Instagram, Yo...
Angela Michelle - phaware® interview 207
November 16, 2018 13:00Angela Michelle is a professional photographer and yoga instructor living in San Antonio, Texas. She was diagnosed with CTEPH in January 2018 after years of experiencing symptoms. Angela underwent PTE surgery in August of 2018 at UCSD. My name is Angela Michelle. I am from San Antonio, Texas, and I was diagnosed with CTEPH, which is a form of pulmonary hypertension. How I was diagnosed is actually quite a story. I began getting short of breath probably about 2013, and I kept bringing it...
Episode 207 - Angela Michelle
November 15, 2018 13:00 - 9 minutes - 9.16 MBAngela Michelle is a professional photographer and yoga instructor living in San Antonio, Texas. She was diagnosed with CTEPH in January 2018 after years of experiencing symptoms. Angela underwent PTE surgery in August of 2018 at UCSD. Learn more about pulmonary hypertension trials at www.phaware.global/clinicaltrials. Never miss an episode with the phaware® podcast app. Follow us @phaware on Facebook, Twitter, Instagram, YouTube & Linkedin Engage for a cure: www.phaware.global/donate #pha...
Robert Frantz, MD - phaware® interview 206
November 13, 2018 13:00Robert P. Frantz is the director of the Mayo Pulmonary Hypertension Clinic, which has a robust referral practice of patients with pulmonary arterial hypertension. Dr. Frantz has served as the Mayo site PI on numerous multicenter trials in PH including the majority of trials resulting in FDA approved PH therapies. He also performs complex hemodynamic studies in the catheterization laboratory including right heart catheterizations for patients with pulmonary arterial hypertension and also pat...
Episode 206 - Robert Frantz, MD
November 12, 2018 13:00 - 10 minutes - 9.59 MBRobert P. Frantz is the director of the Mayo Pulmonary Hypertension Clinic, which has a robust referral practice of patients with pulmonary arterial hypertension. Dr. Frantz has served as the Mayo site PI on numerous multicenter trials in PH including the majority of trials resulting in FDA approved PH therapies. He also performs complex hemodynamic studies in the catheterization laboratory including right heart catheterizations for patients with pulmonary arterial hypertension and also pati...
Jennifer Gendron - phaware® interview 205
November 09, 2018 13:00Canadian caregiver Jennifer Gendron has been working with the pulmonary hypertension community since 2003, when her son Braden was diagnosed at the age of five. She discusses Braden’s PH journey that ultimately led to him having a double-lung transplant at The Hospital for Sick Kids in September 2009. My name is Jennifer Gendron. I am from Hampton, New Brunswick. I am the mom of a young man [Brayden], who was diagnosed with pulmonary hypertension when he was five, and received a double l...
Episode 205 - Jennifer Gendron
November 08, 2018 13:00 - 11 minutes - 12.4 MBCanadian caregiver Jennifer Gendron has been working with the pulmonary hypertension community since 2003, when her son Braden was diagnosed at the age of five. She discusses Braden’s PH journey that ultimately led to him having a double-lung transplant at The Hospital for Sick Kids in September 2009. Learn more about clinical trials at: www.phaware.global/clinicaltrials Never miss an episode with the phaware® podcast app. Follow us @phaware on Facebook, Twitter, Instagram, YouTube & Link...
Janette Reyes, NP - phaware® interview 204
November 06, 2018 13:00Janette Reyes, NP has provided comprehensive care for children with Pulmonary Hypertension at the Hospital for Sick Children since the development of the Pulmonary Hypertension Service in the year 2000. She is involved in research and strives to improve pediatric patients’ quality of life. Janette discusses Child to Adult Transition Guidelines specific to the pulmonary hypertension patient population. I'm Janette Reyes. I'm a nurse practitioner, and I work at the Hospital for Sick Childre...
Episode 204 - Janette Reyes, NP
November 05, 2018 13:00 - 6 minutes - 8 MBJanette Reyes, NP has provided comprehensive care for children with Pulmonary Hypertension at the Hospital for Sick Children since the development of the Pulmonary Hypertension Service in the year 2000. She is involved in research and strives to improve pediatric patients’ quality of life. Janette discusses Child to Adult Transition Guidelines specific to the pulmonary hypertension patient population. Learn more about pulmonary hypertension trials at www.phaware.global/clinicaltrials. Neve...
Sam Bowker and Ken Porter - phaware® interview 203
November 02, 2018 12:00Sam Bowker is a pulmonary hypertension patient on triple therapy from Canada. Ken Porter is her partner and caregiver. They discuss Sam’s diagnosis and creative ways they work together to manage her PH treatment regimen. Sam: My name is Sam Bowker. I'm a patient at the Vancouver PH Clinic. But I live in Victoria. I was diagnosed with pulmonary hypertension almost three years ago. So my diagnosis date is November. Ken: My name is Ken Porter. I'm Sam's partner. We've been together for e...
Episode 203 - Sam Bowker and Ken Porter
November 01, 2018 12:00 - 8 minutes - 9.95 MBSam Bowker is a pulmonary hypertension patient on triple therapy from Canada. Ken Porter is her partner and caregiver. They discuss Sam’s diagnosis and creative ways they work together to manage her PH treatment regimen. Learn more about pulmonary hypertension trials a www.phaware.global/clinicaltrials. Never miss an episode with the phaware® podcast app. Follow us @phaware on Facebook, Twitter, Instagram, YouTube & Linkedin Engage for a cure: www.phaware.global/donate #phaware #YoungwithP...
Natalie Roy - phaware® interview 202
October 30, 2018 12:00Canadian Natalie Roy is a former pulmonary hypertension patient who received a double-lung transplant in September 2017. She discusses having an identity crisis post PH. My name is Natalie Roy. I live in Vancouver, British Columbia, Canada. I was diagnosed with, what was called at the time, primary pulmonary hypertension in 2005 when I was 20. Currently, I am one year past new lungs. I just celebrated my one-year lungiversary. I just started fainting. I started noticing that I was havin...
Episode 202 - Natalie Roy
October 29, 2018 12:00 - 6 minutes - 8.1 MBCanadian Natalie Roy is a former pulmonary hypertension patient who received a double-lung transplant in September 2017. She discusses having an identity crisis post PH. Learn more about pulmonary hypertension trials a www.phaware.global/clinicaltrials. Never miss an episode with the phaware® podcast app. Follow us @phaware on Facebook, Twitter, Instagram, YouTube & Linkedin Engage for a cure: www.phaware.global/donate #phaware #YoungwithPAH #LifeInPurple #PHUnited @PHACanada @antidote_me
Brooke Paulin - phaware® interview 201
October 26, 2018 12:00Canadian Pulmonary Hypertension Patient, Brooke Paulin discusses her road to PH Diagnosis. My name's Brooke Paulin. I am from Mississauga, Ontario, just outside of Toronto. I was diagnosed in February of 2014, so I guess four and a half years ago, just shy of five. I was a competitive athlete growing up. I represented Canada in figure skating, I was a pair skater. So obviously aerobic capacity was pretty much second to none. I "retired", when I was about 21, and it was actually at that ...
Episode 201 - Brooke Paulin
October 25, 2018 12:00 - 7 minutes - 8.59 MBCanadian Pulmonary Hypertension Patient, Brooke Paulin discusses her road to PH Diagnosis. Learn more about pulmonary hypertension trials a www.phaware.global/clinicaltrials. Never miss an episode with the phaware® podcast app. Follow us @phaware on Facebook, Twitter, Instagram, YouTube & Linkedin Engage for a cure: www.phaware.global/donate #phaware #YoungwithPAH @PHACanada @antidote_me
Iain Armstrong - phaware® interview 200
October 23, 2018 12:00Chairman of PHA UK, Iain Armstrong talks about PHawareness Week 2018 (October 22-28), EmPHasis10 and the power of collaboration within the PH Community. My name is Iain Armstrong. I'm chair of PHA UK. I do two jobs, I do that part-time. I'm also consultant nurse in one of the large PH centers in the UK. I've been working in PH now for 20 years. 20 years ago we thought it would be a good idea if some of the patients I had could be put in with other patients by telephone, and from that gr...
Episode 200 - Iain Armstrong, PHA UK
October 22, 2018 12:00 - 5 minutes - 7.3 MBIn this episode, Chairman of PHA UK, Iain Armstrong talks about PHawareness Week 2018 (October 22-28), EmPHasis10 and the power of collaboration within the PH Community. Learn more about clinical trials at: www.phaware.global/clinicaltrials Never miss an episode with the phaware® podcast app. Follow us @phaware on Facebook, Twitter, Instagram, YouTube & Linkedin Engage for a cure: www.phaware.global/donate #phaware #phawareMD @antidote_me @PHA_UK #PHWeek18 #LetsTalkPH
Darren Dempsey - phaware® interview 199
October 19, 2018 12:00Canadian Pulmonary Hypertension Caregiver Darren Dempsey discusses the impact rare disease has had on his family and how stress impacts the entire family. My name is Darren Dempsey. I am a caregiver. My wife, Nicole, was diagnosed with PH five years ago. It's really affected our family more than I could ever imagine. We've had to deal a change in employment. Change in finances. Change in the amount of work that I have to do around the house. But we have managed pretty well in the last fiv...
Episode 199 - Darren Dempsey
October 18, 2018 12:00 - 3 minutes - 5.02 MBCanadian Pulmonary Hypertension Caregiver Darren Dempsey discusses the impact rare disease has had on his family and how stress impacts the entire family. Learn more about pulmonary hypertension trials at www.phaware.global/clinicaltrials. Never miss an episode with the phaware® podcast app. Follow us @phaware on Facebook, Twitter, Instagram, YouTube & Linkedin Engage for a cure: www.phaware.global/donate #phaware @antidote_me @phacanada
Marion Roth - phaware® interview 198
October 16, 2018 12:42Canadian Pulmonary Hypertension Patient, Marion Roth discusses the importance of clinical trials, fearlessly tackling her bucket list and educating the world about #phaware-ness. My name is Marion Roth. I'm a 63 year old lady from Milverton, Ontario. I was diagnosed seven and a half years ago. I'm alive, kicking, and looking for more adventure. I began to believe that I was overweight. I was out of shape, because as I went for my walks daily with my neighbor who is 20 years younger tha...
Episode 198 - Marion Roth
October 15, 2018 12:00 - 6 minutes - 8.28 MBCanadian Pulmonary Hypertension Patient, Marion Roth discusses the importance of clinical trials, fearlessly tackling her bucket list and educating the world about #phaware-ness. Learn more about pulmonary hypertension trials at www.phaware.global/clinicaltrials. Never miss an episode with the phaware® podcast app. Follow us @phaware on Facebook, Twitter, Instagram, YouTube & Linkedin Engage for a cure: www.phaware.global/donate #phaware @antidote_me @phacanada
Kristen Wieneke - phaware® interview 197
October 12, 2018 12:00Kristen Wieneke is a long term pulmonary hypertension survivor. She was diagnosed in 2003 during open heart surgery to repair an ASD. She discusses the stigma that comes with rare disease, the importance of clinical trials and why patients must be their own advocate. I'm Kristen Wieneke, and I'm a pulmonary hypertension patient. I was diagnosed with pulmonary hypertension back in 2003 during open heart surgery to repair an ASD. They confirmed the pulmonary hypertension during surgery when...
Episode 197 - Kristen Wieneke
October 11, 2018 12:00 - 7 minutes - 6.74 MBKristen Wieneke is a long term pulmonary hypertension survivor. She was diagnosed in 2003 during open heart surgery to repair an ASD. She discusses the stigma that comes with rare disease, the importance of clinical trials and why patients must be their own advocate. Learn more about pulmonary hypertension trials at www.phaware.global/clinicaltrials. Never miss an episode with the phaware® podcast app. Follow us @phaware on Facebook, Twitter, Instagram, YouTube & Linkedin Engage for a cure...
Abby Sherwood - phaware® interview 196
October 09, 2018 12:00Abby Sherwood discusses navigating life with pulmonary hypertension on the 15th anniversary of her PH diagnosis. My name is Abby Sherwood, and I am a pulmonary hypertension patient. From what I've been told, I think I was probably starting to slow down. Two-year-olds, they're very energetic and they like to play, and they like to run around and everything. What probably happened was I probably started slowing down, and my parents probably noticed that I was more out of breath than usual...
Episode 196 - Abby Sherwood
October 08, 2018 12:00 - 6 minutes - 7.64 MBAbby Sherwood discusses navigating life with pulmonary hypertension on the 15th anniversary of her PH diagnosis. Learn more about pulmonary hypertension trials at www.phaware.global. Never miss an episode with the phaware® podcast app. Follow us @phaware on Facebook, Twitter, Instagram, YouTube & Linkedin Engage for a cure: www.phaware.global/donate #phaware #pottsshunt #YoungwithPAH
Laurie WItherwax - phaware® interview 195
October 05, 2018 12:00Laurie Witherwax is the Vice President of Project Management at Worldwide Clinical Trials, which provides drug development services from Early Phase and Bioanalytical Sciences, through Phase II, III and IV. In this episode, Laurie discusses the role of CROs (clinical research organizations). Laurie was the Program Director for global Phase III cardiovascular trials encompassing 38 countries across 620 sites, including 3,400 patients, and other trials involving complex and rare diseases. Her...
Episode 195 - Laurie Witherwax
October 04, 2018 12:00 - 5 minutes - 4.97 MBLaurie Witherwax is the Vice President of Project Management at Worldwide Clinical Trials, which provides drug development services from Early Phase and Bioanalytical Sciences, through Phase II, III and IV. In this episode, Laurie discusses the role of CROs (clinical research organizations). Laurie was the Program Director for global Phase III cardiovascular trials encompassing 38 countries across 620 sites, including 3,400 patients, and other trials involving complex and rare diseases. Her ...
Vinicio de Jesus Perez, MD - phaware® interview 194
October 02, 2018 12:00In this episode, Dr. Perez discusses genetic markers in a population of Iberian gypsies, who are afflicted with a very severe form of pulmonary hypertension that is called pulmonary veno-occlusive disease. Vinicio de Jesus Perez, MD is Assistant Professor of Medicine (Pulmonary and Critical Care Medicine) at the Stanford Adult PH Clinic where he trains fellows pursuing careers in PH and IPF. My name is Vinicio de Jesus Perez. I am an assistant professor in the Division of Pulmonary Crit...
Episode 194 - Vinicio A de Jesus Perez, MD
October 01, 2018 12:00 - 8 minutes - 7.7 MBIn this episode, Dr. Perez discusses genetic markers in a population of Iberian gypsies, who are afflicted with a very severe form of pulmonary hypertension that is called pulmonary veno-occlusive disease. Vinicio de Jesus Perez, MD is Assistant Professor of Medicine (Pulmonary and Critical Care Medicine) at the Stanford Adult PH Clinic where he trains fellows pursuing careers in PH and IPF. Learn more about clinical trials at: www.phaware.global/clinicaltrials. Never miss an episode with...
Jessica York - phaware® interview 193
September 28, 2018 12:00Jessica York is a pediatric pulmonary hypertension caregiver to her 6 year old daughter Haylee. In this episode she discusses Hay's diagnosis and the importance of pediatric PH research. Haylee lost her battle with PH on 2/11/2020 Click here to visit Haylee's PHun Walk 4 Hay page. My name is Jessica York and I'm a pulmonary hypertension caregiver. We knew nothing was wrong with Haylee until age three. At her three year old checkup her doctor heard a heart murmur for the first tim...
Episode 193 - Jessica York
September 27, 2018 12:00 - 2 minutes - 2.87 MBJessica York is a pediatric pulmonary hypertension caregiver to her 6 year old daughter Haylee. In this episode she discusses Hay's diagnosis and the importance of pediatric PH research. Haylee York lost her battle with PH on 2/11/2020 Click here to visit Haylee's PHun Walk 4 Hay page. Learn more about clinical trials at: www.phaware.global/clinicaltrials Never miss an episode with the phaware® podcast app. Follow us @phaware on Facebook, Twitter, Instagram, YouTube & Linkedin Engage...
Tom Krohn - phaware® interview 192
September 25, 2018 12:00Tom Krohn is the Chief Development Officer at Antidote. In this episode, Tom details a collaboration between phaware global association® and Antidote Technologies to accelerate lung disease research. This partnership provides pharmaceutical companies with end-to-end clinical trial recruitment services through an extensive network of patients with chronic lung diseases. Tom is an experienced executive leader in multiple healthcare and IT settings including sub-Saharan Africa development, U...
Episode 192 - Tom Krohn
September 24, 2018 12:00 - 10 minutes - 9.46 MBTom Krohn is the Chief Development Officer at Antidote. In this episode, Tom details a collaboration between phaware global association® and Antidote Technologies to accelerate lung disease research. This partnership provides pharmaceutical companies with end-to-end clinical trial recruitment services through an extensive network of patients with chronic lung diseases. Tom is an experienced executive leader in multiple healthcare and IT settings including sub-Saharan Africa development, US...
Maleen Fischer - phaware® interview 191
September 21, 2018 12:00At the age of three, Maleen Fischer was diagnosed with pulmonary hypertension and, as there was no treatment for this fatal disease at the time in Austria, doctors sent her home. Her life expectancy was only a few years. Now, 20 years later, Maleen discusses early diagnosis, the joy of graduating college and the importance of global awareness. My name is Maleen Fischer. I'm from Vienna, Austria. When I was very little, my mom, early on, she noticed when she was breastfeeding me - she just...
Episode 191 - Maleen Fischer
September 20, 2018 12:00 - 10 minutes - 9.43 MBAt the age of three, Maleen Fischer was diagnosed with pulmonary hypertension and, as there was no treatment for this fatal disease at the time in Austria, doctors sent her home. Her life expectancy was only a few years. Now, 20 years later, Maleen discusses early diagnosis, the joy of graduating college and the importance of global awareness. Click here to learn more about Maleen's book: As If There Were No Tomorrow: Hope Springs Eternal. Learn more about pulmonary hypertension at www.p...
Victor F. Tapson, MD - phaware® interview 190
September 18, 2018 12:00Victor F. Tapson, MD discusses the PERT Consortium, a network of multidisciplinary pulmonary embolism response teams working to improve the care of pts w severe PE. The PERT Consortium intends to guide and influence pulmonary embolism (PE) care and research in institutions across the U.S. and will be the driving force behind increased survival rates and the future of PE treatment. I'm Vic Tapson. I'm at Cedar Sinai Medical Center in Los Angeles. I'm in pulmonary critical care medicine and...
Episode 190 - Victor F. Tapson, MD
September 17, 2018 12:00 - 4 minutes - 4.59 MBVictor F. Tapson, MD discusses the PERT Consortium, a network of multidisciplinary pulmonary embolism response teams working to improve the care of pts w severe PE. The PERT Consortium intends to guide and influence pulmonary embolism (PE) care and research in institutions across the U.S. and will be the driving force behind increased survival rates and the future of PE treatment. Learn more about pulmonary hypertension at www.phaware365.global. Never miss an episode with the phaware® podc...
Vallerie McLaughlin, MD - phaware® interview 189
September 14, 2018 12:00Vallerie McLaughlin, MD from Michigan Medicine's Cardiovascular Center explains the basics of clinical trials in part 2 of her discussion. Dr. McLaughlin is the Director of the Pulmonary Hypertension Program at the University of Michigan in Ann Arbor. She is a Fellow of the American College of Cardiology, American College of Chest Physicians, and American Heart Association (AHA). Dr. McLaughlin has been the Principal Investigator of several major clinical trials of drug therapies for pulmon...
Episode 189 - Vallerie McLaughlin, MD
September 13, 2018 12:00 - 11 minutes - 10.6 MBVallerie McLaughlin, MD from Michigan Medicine's Cardiovascular Center explains the basics of clinical trials in part 2 of her discussion. Dr. McLaughlin is the Director of the Pulmonary Hypertension Program at the University of Michigan in Ann Arbor. She is a Fellow of the American College of Cardiology, American College of Chest Physicians, and American Heart Association (AHA). Dr. McLaughlin has been the Principal Investigator of several major clinical trials of drug therapies for pulmona...
Vallerie McLaughlin, MD - phaware® interview 188
September 11, 2018 12:00Vallerie McLaughlin, MD from Michigan Medicine's Cardiovascular Center breaks down the different phases of clinical trials in part 1 of her discussion. Dr. McLaughlin is the Director of the Pulmonary Hypertension Program at the University of Michigan in Ann Arbor. She is a Fellow of the American College of Cardiology, American College of Chest Physicians, and American Heart Association (AHA). Dr. McLaughlin has been the Principal Investigator of several major clinical trials of drug therapi...
Episode 188 - Vallerie McLaughlin, MD
September 10, 2018 12:00 - 7 minutes - 6.92 MBVallerie McLaughlin, MD from Michigan Medicine's Cardiovascular Center breaks down the different phases of clinical trials in part 1 of her discussion. Dr. McLaughlin is the Director of the Pulmonary Hypertension Program at the University of Michigan in Ann Arbor. She is a Fellow of the American College of Cardiology, American College of Chest Physicians, and American Heart Association (AHA). Dr. McLaughlin has been the Principal Investigator of several major clinical trials of drug therapie...