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
Episode 237 - Alejandra Hernandez
April 11, 2019 12:30 - 9 minutes - 10.3 MBPulmonary hypertension patient, Alejandra Hernandez discusses being diagnosed with PH in the 9th week of pregnancy and the power of acceptance while battling this rare disease. 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 #ClinicalTrials @antidote_me
Samantha Ramirez - phaware® interview 236
April 09, 2019 12:30Former pulmonary hypertension patient and lung transplant recipient, Samantha Ramirez discusses her PH diagnosis because of over-the-counter diet pills and the need for continued need for PH awareness. Hi, my name is Samantha Ramirez and I'm from Orange County, California. I was diagnosed with pulmonary hypertension back in April, 2006. My weight has always been a battle for me since I was a teenager. Off and on through high school, I used diet pills. Back in that time, lots of young la...
Episode 236 - Samantha Ramirez
April 08, 2019 12:30 - 9 minutes - 10.7 MBFormer pulmonary hypertension patient and lung transplant recipient, Samantha Ramirez discusses her PH diagnosis because of over-the-counter diet pills and the need for continued need for PH awareness. 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 #ClinicalTrials @antidote_me
Aryeh Copperman - phaware® interview 235
April 05, 2019 12:00CEO of Pulmonary Hypertension Association Israel, Aryeh Cooperman on his role as a caregiver for his wife and why advocating and raising awareness is important for pulmonary hypertension patients. http://www.phisrael.org.il/ My name is Aryeh Cooperman. I'm the CEO of the PH Association in Israel, and I'm a caregiver of my wife. In Israel, most of the patients, nearly 100% of the patients when they came the first time to a physician and they had symptoms of PH, their physician told them th...
Episode 235 - Aryeh Cooperman
April 04, 2019 13:45 - 8 minutes - 10.1 MBCEO of Pulmonary Hypertension Association Israel, Aryeh Cooperman on his role as a caregiver for his wife and why advocating and raising awareness is important for pulmonary hypertension patients. http://www.phisrael.org.il/ 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 #Clini...
David Stott - phaware® interview 234
April 02, 2019 12:00David Stott is a 42 year old musician and operating theatre practitioner from north west England. David was diagnosed with IPAH in August 2013. He discusses his road to diagnosis and how it led to his band Ward XVI. My name is David Stott. I'm from Northwest of England. I was diagnosed 5-1/2 years ago with idiopathic pulmonary hypertension, and it came out of the blue. I was 36. I was diagnosed quite quickly, really. I'd been quite active and quite very fit for all my life playing lots...
Episode 234 - David Stott
April 01, 2019 12:00 - 5 minutes - 7.23 MBDavid Stott is a 42 year old musician and operating theatre practitioner from north west England. David was diagnosed with IPAH in August 2013. He discusses his road to diagnosis and how it led to his band Ward XVI. 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 #ClinicalTrials...
Stacey Barta - phaware® interview 233
March 29, 2019 12:00Pulmonary hypertension patient, Stacey Barta discusses how she refused to give up on being a preschool teacher after being put on disability following her diagnosis and why early diagnosis and PH awareness is critical for medical professionals. My name is Stacey Barta, and I'm a pulmonary hypertension patient. In 2004, I was diagnosed with an autoimmune disease, they kind of went back and forth between lupus and mixed connective tissue disease, and every time I saw a new doctor they'd c...
Episode 233 - Stacey Barta
March 28, 2019 12:00 - 7 minutes - 7.23 MBPulmonary hypertension patient, Stacey Barta discusses how she refused to give up on being a preschool teacher after being put on disability following her diagnosis and why early diagnosis and PH awareness is critical for medical professionals. 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/do...
Sarah Brackett - phaware® interview 232
March 26, 2019 12:00Pulmonary hypertension patient Sarah Brackett discusses her devastating road to diagnosis, busting CTEPH through surgery and the importance of educating medical professions in rural areas to raise rare disease awareness. My name is Sarah Brackett. I live in Manassas, Virginia. In my life, as far back as 1985, I've had 3 pulmonary emboluses, two of them following surgeries after a Greenfield filter was put in to prevent them. And within six months of the last one in 2004, I started getting...
Episode 232 - Sarah Brackett
March 25, 2019 12:00 - 12 minutes - 13 MBIn this episode, pulmonary hypertension patient Sarah Brackett discusses her devastating road to diagnosis, busting CTEPH through surgery and the importance of educating medical professions in rural areas to raise rare disease awareness. 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 #p...
Joellen Brown - phaware® interview 231
March 22, 2019 12:00Pulmonary hypertension patient Joellen Brown discusses being born with a hole in her heart in 1956 that developed into a PH diagnosis in 2009 and the importance of support groups and PH research. My name is Joellen Brown, and I am a pulmonary hypertension patient. I am from Columbus, Ohio. I was diagnosed with PH 2009, but that's not where my journey started. I was born with a hole in my heart, back in 1956. So not a lot of treatment, not a lot of surgeries that went well. I was one of ...
Episode 231 - Joellen Brown
March 21, 2019 14:53 - 5 minutes - 7.22 MBIn this episode, pulmonary hypertension patient Joellen Brown discusses being born with a hole in her heart in 1956 that developed into a PH diagnosis in 2009 and the importance of support groups and PH research. My name is Joellen Brown, and I am a pulmonary hypertension patient. I am from Columbus, Ohio. I was diagnosed with PH 2009, but that's not where my journey started. I was born with a hole in my heart, back in 1956. So not a lot of treatment, not a lot of surgeries that went wel...
Hollie Satona - phaware® interview 230
March 19, 2019 12:00Pediatric pulmonary hypertension caregiver, Hollie Satona discusses her son Joelan's PH diagnosis and the challenge of juggling caregiving because three of her four children are impacted by rare disease and special needs. I'm Hollie Satona and I am the parent and caregiver of my son who is eight years old, Joelan, who has severe pulmonary hypertension. It's been kind of a whirlwind for JoJo since the day he was born. I didn't know about pulmonary hypertension until about two years ago. ...
Episode 230 - Hollie Satona
March 18, 2019 12:00 - 5 minutes - 7.33 MBIn this episode, pediatric pulmonary hypertension caregiver, Hollie Satona discusses her son Joelan's PH diagnosis and the challenge of juggling caregiving because three of her four children are impacted by rare disease and special needs. 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 #...
Barbara Thompson - phaware® interview 229
March 15, 2019 12:00Pulmonary hypertension patient Barbara Thompson discusses why she wears zebra clothing 365 days a year and her long road through 14 doctors before a young grad student gave her a proper PH diagnosis. Hi, I'm Barbara Thompson. I'm a pulmonary hypertension patient. We used to do weddings as a family business. We did everything: photography, video, cakes, catering, flowers, directing, reception hall, chapel. But the last thing I remember in April of 2000, was getting a bride down the aisle...
Episode 229 - Barbara Thompson
March 14, 2019 12:00 - 4 minutes - 6.24 MBIn this episode, pulmonary hypertension patient Barbara Thompson discusses why she wears zebra clothing 365 days a year and her long road through 14 doctors before a young grad student gave her a proper PH diagnosis. 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 #ClinicalTrial...
Diane Dauwalder - phaware® interview 228
March 12, 2019 12:00Pulmonary hypertension patient Diane Dauwalder discusses how she became symptomatic in 2002, preparing for the end of her life, and how thanks to PH research and new therapies how she adjusted to a new normal. Hi, my name's Diane Dauwalder. I'm a pulmonary hypertension patient, and I'm from Fort Worth, Texas. I'm the Fort Worth support group leader. I was confirmed diagnosed in February of 2005, but I started to become symptomatic around 2002 when I moved from Arizona to Colorado. Every...
Episode 228 - Diane Dauwalder
March 11, 2019 12:00 - 4 minutes - 3.98 MBIn this episode, pulmonary hypertension patient Diane Dauwalder discusses how she became symptomatic in 2002, preparing for the end of her life, and how thanks to PH research and new therapies how she adjusted to 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/donate #phaware #Cli...
Alleena Shiwdas - phaware® interview 227
March 08, 2019 13:00In this episode, pulmonary hypertension patient, Alleena Shiwdas discusses the importance of a good peer support network and how psychological care as critical part of a PH treatment plan. My name is Alleena Shiwdas, and I'm a pulmonary hypertension patient. It was the day after I had my second son. I was in the hospital. I had a C-section and they told me I had to get up and walk. I said okay. Besides the fact that I was in a lot of pain, I was unable to breath. I couldn't walk five fe...
Episode 227 - Alleena Shiwdas
March 07, 2019 13:00 - 5 minutes - 4.81 MBIn this episode, pulmonary hypertension patient, Alleena Shiwdas discusses the importance of a good peer support network and how psychological care as critical part of a PH treatment plan. 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 #ClinicalTrials @antidote_me
Alexis Trotter - phaware® interview 226
March 05, 2019 13:00Pulmonary hypertension patient Alexis Trotter discusses living on oxygen 24/7, her passion for hula dancing, what inspired her to become a cardiac sonographer and her love of Camp del Corazon. Hi. My name is Alexis Trotter, and I am a pulmonary hypertension patient. I was born with a congenital heart defect and I had my repair when I was four years old. However, after my surgery, I remained symptomatic. The doctors told my parents that I was just doing it for attention. Finally, my mom ...
Episode 226 - Alexis Trotter
March 04, 2019 13:00 - 5 minutes - 6.67 MBIn this episode, pulmonary hypertension patient Alexis Trotter discusses living on oxygen 24/7, her passion for hula dancing, what inspired her to become a cardiac sonographer and her love of Camp del Corazon. 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 #YoungwithPAH #Clinic...
Gwendolyn R. Brown - phaware® interview 225
March 01, 2019 13:00In this episode, 40 year long-term pulmonary hypertension survivor Gwendolyn R. Brown discusses the importance of clinical trials, building a great PH care team, and how THE LION KING is a perfect metaphor for PH. Hi, my name is Gwendolyn R. Brown, and I am a 40 year survivor with pulmonary hypertension. When I was diagnosed at that time, there was nothing out there. For three years prior, I was getting sick, I thought it was a cold. And I kept going to the doctor, and then they diagnos...
Episode 225 - Gwendolyn R. Brown
February 28, 2019 13:00 - 4 minutes - 6.22 MBIn this episode, 40 year long-term pulmonary hypertension survivor Gwendolyn R. Brown discusses the importance of clinical trials, building a great PH care team, and how THE LION KING is a perfect metaphor for PH. 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 #ClinicalTrials @...
Judith Moatti - phaware® interview 224
February 26, 2019 13:00In this episode, PHA Canada ambassador Judith Moatti discusses the importance of early diagnosis and awareness. Judith was first diagnosed with Pulmonary Arterial Hypertension (PAH) in 2009, at the young age of 25. After a long road to stability and coping with her new reality, she has become a strong advocate and spokesperson for those affected by PAH. Locally, she became a patient representative for Foundation HTAPQ (a Québec-based patient support organization) in 2012. And she also works...
Episode 224 - Judith Moatti
February 25, 2019 13:00 - 5 minutes - 5.19 MBIn this episode, PHA Canada ambassador Judith Moatti discusses the importance of early diagnosis and awareness. Judith was first diagnosed with Pulmonary Arterial Hypertension (PAH) in 2009, at the young age of 25. After a long road to stability and coping with her new reality, she has become a strong advocate and spokesperson for those affected by PAH. Locally, she became a patient representative for Foundation HTAPQ (a Québec-based patient support organization) in 2012. And she also works ...
Kathleen Richardson - phaware® interview 223
February 22, 2019 13:00Pulmonary hypertension patient, Kathleen Richardson, discusses exercise, Team PHenomenal Hope and why research is critical. Hi, I'm Kathleen Richardson, and I am a pulmonary hypertension patient. It was after my son was born, my youngest son, he was about two years old, and I was feeling some shortness of breath. It seemed odd to me, but it wasn't significant. I just figured it was after having three children and feeling a little bit short of breath. But then I went to SeaWorld with som...
Episode 223 - Kathleen Richardson
February 21, 2019 13:00 - 5 minutes - 5.6 MBIn this episode, pulmonary hypertension patient, Kathleen Richardson, discusses exercise, Team PHenomenal Hope and why research is critical. Learn more about pulmonary hypertension 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 @antidote_me @accpchest #phaware @TeamPHHope
Merle Reeseman - phaware® interview 222
February 19, 2019 13:00Pulmonary hypertension patient Merle Reeseman discusses her PH diagnosis and the importance of being seen by a PH specialist who understands the disease and can diagnose and prescribe the proper medication. I'm Merle Reeseman and a pulmonary hypertension patient. It was back probably in the late 90s. I wasn't feeling well, I was a very active person [who] went from this doctor to the next doctor. And one doctor says, "You need to see a specialist." I went to a cardiologist and he said,...
Episode 222 - Merle Reeseman
February 18, 2019 13:00 - 5 minutes - 7.41 MBIn this episode, pulmonary hypertension patient, Merle Reeseman, discusses her PH diagnosis and the importance of being seen by a PH specialist who understands the disease and can diagnose and prescribe the proper medication. Read Merle's Poem in the "Bonus Content" tab. Learn more about pulmonary hypertension 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.glo...
Kevin Burke - phaware® interview 221
February 15, 2019 13:00Australian pulmonary hypertension patient Kevin Burke discusses his PH diagnosis and dealing with depression. My name is Kevin Burke. I'm from Australia and I'm a pulmonary hypertension patient. In 2010, I was diagnosed with pulmonary hypertension. I just was getting short of breath, probably like most people do over a number of years. But being a man, never went to the doctor. I was old, unfit, not playing sport anymore and working shift work, so I put all those excuses together. It wa...
Episode 221 - Kevin Burke
February 14, 2019 13:00 - 7 minutes - 7.48 MBIn this episode, Australian pulmonary hypertension patient Kevin Burke discusses his PH diagnosis and dealing with depression. Learn more about pulmonary hypertension 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 @phaaustralia @antidote_me @accpchest #phaware
Scott Visovatti, MD - phaware® interview 220
February 12, 2019 13:00Scott Visovatti, MD discusses how early treatment of patients with abnormal exercise studies can delay, or even prevent, the development of pulmonary arterial hypertension. Dr. Visovatti is an Assistant Professor of Internal Medicine in the Division of Cardiology at the University of Michigan. As a physician-scientist in their Pulmonary Hypertension Program, he cares for patients in clinic, performs clinical research that investigates the role of exercise in the diagnosis of pulmonary hyper...
Episode 220 - Scott Visovatti, MD
February 11, 2019 13:00 - 9 minutes - 10.5 MBIn this episode, Scott Visovatti, MD discusses how early treatment of patients with abnormal exercise studies can delay, or even prevent, the development of pulmonary arterial hypertension. Dr. Visovatti is an Assistant Professor of Internal Medicine in the Division of Cardiology at the University of Michigan. As a physician-scientist in their Pulmonary Hypertension Program, he cares for patients in clinic, performs clinical research that investigates the role of exercise in the diagnosis of...
Valerie McLaughlin, MD - phaware® interview 219
February 08, 2019 13:00Vallerie McLaughlin, MD from Michigan Medicine's Cardiovascular Center discusses what a pulmonary hypertension patients should expect in their first visit to an expert PH Center. 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 clin...
Episode 219 - Vallerie McLaughlin, MD
February 07, 2019 13:00 - 6 minutes - 6.19 MBIn this episode, Vallerie McLaughlin, MD from Michigan Medicine's Cardiovascular Center discusses what a pulmonary hypertension patients should expect in their first visit to an expert PH Center. 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 se...
Valerie McLaughlin, MD - phaware® interview 218
February 05, 2019 13:00Vallerie McLaughlin, MD gives an overview of 6th World Symposium on Pulmonary Hypertension, which took place in Nice, France, in early 2018. 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 pulm...
Episode 218 - Vallerie McLaughlin, MD
February 04, 2019 13:00 - 10 minutes - 10.1 MBIn this episode, Vallerie McLaughlin, MD gives an overview of 6th World Symposium on Pulmonary Hypertension, which took place in Nice, France, in early 2018. 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 th...
Vikas Aggarwal, MBBS, MPH - phaware® interview 217
February 01, 2019 13:00In this episode, Dr. Vikas Aggarwal discusses balloon pulmonary angioplasty as a treatment for CTEPH patients. Dr. Aggarwal is a board certified interventional cardiologist and Endovascular Interventional specialist. He directs the interventional vascular medicine program within the division of cardiology at the University of Michigan Hospital in Ann Arbor. Dr. Aggarwal specializes in percutaneous therapies for Deep Vein and Pulmonary Thromboembolic disease including catheter based thrombus ...
Episode 217 - Vikas Aggarwal, MBBS MPH
January 31, 2019 13:00 - 7 minutes - 7.18 MBIn this episode, Dr. Vikas Aggarwal discusses balloon pulmonary angioplasty as a treatment for CTEPH patients. Dr. Aggarwal is a board certified interventional cardiologist and Endovascular Interventional specialist. He directs the interventional vascular medicine program within the division of cardiology at the University of Michigan Hospital in Ann Arbor. Dr. Aggarwal specializes in percutaneous therapies for Deep Vein and Pulmonary Thromboembolic disease including catheter based thrombus ...
Jonathan Haft, MD - phaware® interview 216
January 29, 2019 13:00Jonathan Haft, MD discusses PTE (pulmonary thromboendarterectomy) surgery, which is the potentially curative operation offered for some patients with chronic thromboembolic pulmonary hypertension (CTEPH). Dr. Haft has been the director of Michigan’s internationally recognized ECMO program since 2005. He is also the Associate Director of the Cardiovascular Intensive Care unit, and is the Chief of Cardiothoracic Surgery at the Ann Arbor VA Hospital. My name is Jonathan Haft. I am a physici...
Episode 216 - Jonathan Haft, MD
January 28, 2019 13:00 - 10 minutes - 9.77 MBIn this episode, Jonathan Haft, MD discusses PTE (pulmonary thromboendarterectomy) surgery, which is the potentially curative operation offered for some patients with chronic thromboembolic pulmonary hypertension (CTEPH). Dr. Haft has been the director of Michigan’s internationally recognized ECMO program since 2005. He is also the Associate Director of the Cardiovascular Intensive Care unit, and is the Chief of Cardiothoracic Surgery at the Ann Arbor VA Hospital. Learn more about pulmona...
Marc de Perrot, MD phaware® interview 215
January 25, 2019 13:00Dr. Marc de Perrot joined the Division of Thoracic Surgery as a staff surgeon and Assistant Professor at the University of Toronto in 2005. In 2009, he was appointed Associate Professor of Surgery based on his research and clinical work. Dr. de Perrot’s surgical expertise focuses on surgery for end-stage lung diseases such as lung and heart-lung transplantation as well as pulmonary endarterectomy for chronic thromboembolic pulmonary hypertension. He is also the Head of the Toronto Mesothe...
Episode 215 - Marc de Perrot, MD
January 24, 2019 13:00 - 9 minutes - 8.82 MBDr. Marc de Perrot joined the Division of Thoracic Surgery as a staff surgeon and Assistant Professor at the University of Toronto in 2005. In 2009, he was appointed Associate Professor of Surgery based on his research and clinical work. Dr. de Perrot’s surgical expertise focuses on surgery for end-stage lung diseases such as lung and heart-lung transplantation as well as pulmonary endarterectomy for chronic thromboembolic pulmonary hypertension. He is also the Head of the Toronto Mesothel...
Angela Bates, MD - phaware® interview 214
January 22, 2019 13:00Dr. Angela Bates is pediatric PH specialist from Stollery Children’s Hospital. She is committed to conducting research in pediatric patients in the areas of critical care, specifically those with congenital heart disease and those affected by infectious diseases in the critical care arena, as well as patients presenting with pulmonary hypertension of all etiologies. Her research is focused on improving diagnosis, treatment, outcomes and resources available to these patients. In this episode...
Angela Bates, MD - phaware® interview 214
January 22, 2019 13:00Dr. Angela Bates is pediatric PH specialist from Stollery Children’s Hospital. She is committed to conducting research in pediatric patients in the areas of critical care, specifically those with congenital heart disease and those affected by infectious diseases in the critical care arena, as well as patients presenting with pulmonary hypertension of all etiologies. Her research is focused on improving diagnosis, treatment, outcomes and resources available to these patients. In this episode...
Episode 214 - Angela Bates, MD
January 21, 2019 13:00 - 5 minutes - 5.43 MBDr. Angela Bates is pediatric PH specialist from Stollery Children’s Hospital. She is committed to conducting research in pediatric patients in the areas of critical care, specifically those with congenital heart disease and those affected by infectious diseases in the critical care arena, as well as patients presenting with pulmonary hypertension of all etiologies. Her research is focused on improving diagnosis, treatment, outcomes and resources available to these patients. In this episode,...
John Granton, MD - phaware® interview 213
January 18, 2019 13:00Dr. John Granton the head of Respirology at University Health Network, Mount Sinai Hospital and Women’s College Hospital. He is a consultant in respirology and critical care at the Toronto General Hospital and Professor of Medicine at the University of Toronto. He established and remains the director of the pulmonary hypertension (PH) program at the University Health Network. In this episode, Dr. Granton discusses the importance of early diagnosis. My name is John Granton. I'm a lung doc...
Episode 213 - John Granton, MD
January 17, 2019 13:00 - 6 minutes - 6.03 MBDr. John Granton the head of Respirology at University Health Network, Mount Sinai Hospital and Women’s College Hospital. He is a consultant in respirology and critical care at the Toronto General Hospital and Professor of Medicine at the University of Toronto. He established and remains the director of the pulmonary hypertension (PH) program at the University Health Network. In this episode, Dr. Granton discusses the importance of early diagnosis. Learn more about pulmonary hypertension ...