Mackenzie Doyle's guest appearances

Mackenzie Doyle

This is HCD - Human Centered Design Podcast

Bringing Design Closer with Gerry Scullion

Medical Error Interviews

The Human Centered Design Podcast 

Sarah Drummond

Josina Vink

Award Winner Producer

Amy Bucher

Tomer Sharon

Dana Chisnell

Georgie Smallwood

Belina Raffy

Victor Rodrigues

Sarah Richards

Kelly Ann McKercher

Patrick Quattlebaum

Jane Hession

Laura Kalbag

Greg Bernarda

OwlTail

Kim MacKenzie

This episode is brought to you by This is Doing - Learn Design and Innovation remotely via online classes Hello and welcome to another episode of Bringing Design Closer. My name is Gerry Scullion, and I’m a service designer, and founder of This is HCD and CEO of This is Doing - we provide live online design and innovation classes, providing training for service designers, design researchers, product managers, user experience designers and much more.Today on the show we have Kim Mackenzie Doyle, a name that will be familiar to all of the Irish Design community. Kim is the Former President of the Irish Design Institute and when I say this, I truly mean it, one of the most incredibly forward-thinking individuals in Ireland right now. Kim works tirelessly on projects that she initiated such as Mind Over Matter, and also Why Design - an initiative that aims to address and improve the ration of men and women in Design. We also speak about Kim’s latest project, The Big Idea, something I am involved with as a judge, and This is HCD and This is Doing are both right behind her on this one - working on the next generation of designers currently in School.  Let’s get into the episode...  The Big Idea Kim on LinkedIn Kim on Twitter      Learn more about your ad choices. Visit megaphone.fm/adchoices

This episode is brought to you by <a href="https://www.thisisdoing.com/?thisishcd" rel="nofollow" target="_blank">This is Doing - Learn Design and Innovation</a> remotely via online classes Hello and welcome to another episode of Bringing Design Closer. My name is Gerry Scullion, and I’m a service designer, and founder of This is HCD and CEO of This is Doing - we provide live online design and innovation classes, providing training for service designers, design researchers, product managers, user experience designers and much more. Today on the show we have Kim Mackenzie Doyle, a name that will be familiar to all of the Irish Design community. Kim is the Former President of the Irish Design Institute and when I say this, I truly mean it, one of the most incredibly forward-thinking individuals in Ireland right now.  Kim works tirelessly on projects that she initiated such as Mind Over Matter, and also Why Design - an initiative that aims to address and improve the ration of men and women in Design. We also speak about Kim’s latest project, The Big Idea, something I am involved with as a judge, and This is HCD and This is Doing are both right behind her on this one - working on the next generation of designers currently in School.  Let’s get into the episode... <ul> <li><a href="https://www.thebigidea.ie" rel="nofollow" target="_blank">The Big Idea</a></li> <li><a href="https://www.linkedin.com/in/kim-mackenzie-doyle-fidi-4a2b6650/?originalSubdomain=ie" rel="nofollow" target="_blank">Kim on LinkedIn</a></li> <li><a href="https://www.twitter.com/kimmacdoy" rel="nofollow" target="_blank">Kim on Twitter</a></li> </ul> Learn more about your ad choices. Visit <a href="https://megaphone.fm/adchoices" rel="nofollow" target="_blank">megaphone.fm/adchoices</a>

Kim Mackenzie Doyle 'Designing for the future with children and schools at the Center'

This episode is brought to you by This is Doing - Learn Design and Innovation remotely via online classes Hello and welcome to another episode of Bringing Design Closer. My name is Gerry Scullion, and I’m a service designer, and founder of This is HCD and CEO of This is Doing - we provide live online design and innovation classes, providing training for service designers, design researchers, product managers, user experience designers and much more.Today on the show we have Kim Mackenzie Doyle, a name that will be familiar to all of the Irish Design community. Kim is the Former President of the Irish Design Institute and when I say this, I truly mean it, one of the most incredibly forward-thinking individuals in Ireland right now. Kim works tirelessly on projects that she initiated such as Mind Over Matter, and also Why Design - an initiative that aims to address and improve the ration of men and women in Design. We also speak about Kim’s latest project, The Big Idea, something I am involved with as a judge, and This is HCD and This is Doing are both right behind her on this one - working on the next generation of designers currently in School.  Let’s get into the episode...  The Big Idea Kim on LinkedIn Kim on Twitter     See omnystudio.com/listener for privacy information.

This episode is brought to you by <a href="https://www.thisisdoing.com/?thisishcd" rel="nofollow" target="_blank">This is Doing - Learn Design and Innovation</a> remotely via online classes Hello and welcome to another episode of Bringing Design Closer. My name is Gerry Scullion, and I’m a service designer, and founder of This is HCD and CEO of This is Doing - we provide live online design and innovation classes, providing training for service designers, design researchers, product managers, user experience designers and much more. Today on the show we have Kim Mackenzie Doyle, a name that will be familiar to all of the Irish Design community. Kim is the Former President of the Irish Design Institute and when I say this, I truly mean it, one of the most incredibly forward-thinking individuals in Ireland right now.  Kim works tirelessly on projects that she initiated such as Mind Over Matter, and also Why Design - an initiative that aims to address and improve the ration of men and women in Design. We also speak about Kim’s latest project, The Big Idea, something I am involved with as a judge, and This is HCD and This is Doing are both right behind her on this one - working on the next generation of designers currently in School.  Let’s get into the episode... <ul> <li><a href="https://www.thebigidea.ie" rel="nofollow" target="_blank">The Big Idea</a></li> <li><a href="https://www.linkedin.com/in/kim-mackenzie-doyle-fidi-4a2b6650/?originalSubdomain=ie" rel="nofollow" target="_blank">Kim on LinkedIn</a></li> <li><a href="https://www.twitter.com/kimmacdoy" rel="nofollow" target="_blank">Kim on Twitter</a></li> </ul> See <a href="https://omnystudio.com/listener" rel="nofollow" target="_blank">omnystudio.com/listener</a> for privacy information.

Mack Doyle has been sickly since birth -- and along the way medicine gave her numerous diagnoses to explain her symptoms, none of which turned out to be correct. When Mack’s allergy skin tests showed her positive to over 140 foods, grasses, and pollen, the doctor didn’t believe it. “Impossible” he said.  He told Mack she wasn’t allergic to anything, she just had irritable bowel syndrome. But Mack had ‘been there, done’ that with an IBS misdiagnosis before and was adamant she had allergies. Turns out the patient was right -- she just needed a doctor who could connect the dots of Mack’s various symptoms that pointed to mast cell activation syndrome (MCAS), essentially an overactive immune response by our mast cells. Part of the problem of getting a diagnosis was that MCAS was not officially recognized until 2007, so even today very few physicians are aware of the disease. That means patients spend many years and a lot of money trying to get a diagnosis and treatment.  It also means a lot of undiagnosed MCAS patients face repeated gaslighting by physicians in a health care system that quickly defaults to the harmful trope ‘in your head’ for illnesses they can’t immediately diagnose. Mack not only shares her health care journey experiences in finally getting a correct diagnosis, but also what she’s learned about the myriad ways MCAS can manifest.  If -- like me -- you have weird symptoms that doctors couldn’t explain or dismissed as ‘in your head’ -- then you’ll want to hear what Mack has learned about our mast cells and how you can manage them better. Connect with Mack: Twitter: https://twitter.com/MackWithMast GoFundMe:  https://gofundme.com/f/help-mackenzie-fight-mast-cell-disease… Facebook Group: https://facebook.com/groups/MastCell Personal Facebook: https://facebook.com/mackenzie.doyle.12 Be a podcast patron Support Medical Error Interviews on Patreon by becoming a Patron for $2 / month for audio versions.  Premium Patrons get access to video versions of podcasts for $5 / month. Be my Guest I am always looking for guests to share their medical error experiences so we help bring awareness and make patients safer. If you are a survivor, a victim’s surviving family member, a health care worker, advocate, researcher or policy maker and you would like to share your experiences, please send me an email with a brief description:  RemediesPodcast@gmail.com  Need a Counsellor? Like me, many of my clients at Remedies Counseling have experienced the often devastating effects of medical error. If you need a counsellor for your experience with medical error, or living with a chronic illness(es), I offer online video counseling appointments. **For my health and life balance, I limit my number of counseling clients.**  Email me to learn more or book an appointment:  RemediesOnlineCounseling@gmail.com  Scott Simpson:  Counsellor + Patient Advocate + (former) Triathlete I am a counsellor, patient advocate, and - before I became sick and disabled - a passionate triathlete. Work hard. Train hard. Rest hard. I have been living with HIV since 1998. I was the first person living with HIV to compete at the triathlon world championships. Thanks to research and access to medications, HIV is not a problem in my life. I have been living with ME (myalgic encephalomyelitis) since 2012, and thanks in part to medical error, it is a big problem in my life. Counseling / Research I first became aware of the ubiquitousness of medical error during a decade of community based research working with the HIV Prevention Lab at Ryerson University, where I co-authored two research papers on a counseling intervention for people living with HIV, here and here.  Patient participants would often report varying degrees of medical neglect, error and harms as part of their counseling sessions. Patient Advocacy I am co-founder of the ME patient advocacy non-profit Millions Missing Canada, and on the Executive Committee of the Interdisciplinary Canadian Collaborative Myalgic Encephalomyelitis Research Network. I am also a patient advisor for Health Quality Ontario’s Patient and Family Advisory Council, and member of Patients for Patient Safety Canada. Medical Error Interviews podcast and vidcast emerged to give voice to victims, witnesses and participants in this hidden epidemic so we can create change toward a safer health care system. My golden retriever Gladys is a constant source of love and joy. I hope to be well enough again one day to race triathlons again. Or even shovel the snow off the sidewalk.

Mack Doyle has been sickly since birth -- and along the way medicine gave her numerous diagnoses to explain her symptoms, none of which turned out to be correct. When Mack’s allergy skin tests showed her positive to over 140 foods, grasses, and pollen, the doctor didn’t believe it. “Impossible” he said.  He told Mack she wasn’t allergic to anything, she just had irritable bowel syndrome. But Mack had ‘been there, done’ that with an IBS misdiagnosis before and was adamant she had allergies. Turns out the patient was right -- she just needed a doctor who could connect the dots of Mack’s various symptoms that pointed to mast cell activation syndrome (MCAS), essentially an overactive immune response by our mast cells. Part of the problem of getting a diagnosis was that MCAS was not officially recognized until 2007, so even today very few physicians are aware of the disease. That means patients spend many years and a lot of money trying to get a diagnosis and treatment.  It also means a lot of undiagnosed MCAS patients face repeated gaslighting by physicians in a health care system that quickly defaults to the harmful trope ‘in your head’ for illnesses they can’t immediately diagnose. Mack not only shares her health care journey experiences in finally getting a correct diagnosis, but also what she’s learned about the myriad ways MCAS can manifest.  If -- like me -- you have weird symptoms that doctors couldn’t explain or dismissed as ‘in your head’ -- then you’ll want to hear what Mack has learned about our mast cells and how you can manage them better. Connect with Mack: Twitter:<a href="https://twitter.com/MackWithMast" rel="nofollow" target="_blank"> https://twitter.com/MackWithMast</a> GoFundMe: <a href="https://t.co/iKQt1MYwON?amp=1" rel="nofollow" target="_blank"> https://gofundme.com/f/help-mackenzie-fight-mast-cell-disease…</a> Facebook Group:<a href="https://t.co/xsOYDVoavv?amp=1" rel="nofollow" target="_blank"> https://facebook.com/groups/MastCell</a> Personal Facebook:<a href="https://t.co/sudmb6vFJP?amp=1" rel="nofollow" target="_blank"> https://facebook.com/mackenzie.doyle.12</a> Be a podcast patron Support <a href="https://www.patreon.com/rss/MedicalErrorInterviews?auth=2eY8hVY9bd5o78a8cmpNSURYZ2VrqXrq" rel="nofollow" target="_blank">Medical Error Interviews on Patreon</a> by becoming a Patron for $2 / month for audio versions.  Premium Patrons get access to video versions of podcasts for $5 / month. Be my Guest I am always looking for guests to share their medical error experiences so we help bring awareness and make patients safer. If you are a survivor, a victim’s surviving family member, a health care worker, advocate, researcher or policy maker and you would like to share your experiences, please send me an email with a brief description:  <a href="mailto:RemediesPodcast@gmail.com">RemediesPodcast@gmail.com</a> Need a Counsellor? Like me, many of my clients at <a href="https://remediescounseling.com/" rel="nofollow" target="_blank">Remedies Counseling</a> have experienced the often devastating effects of medical error. If you need a counsellor for your experience with medical error, or living with a chronic illness(es), I offer online video counseling appointments. **For my health and life balance, I limit my number of counseling clients.**  Email me to learn more or book an appointment:  <a href="mailto:RemediesOnlineCounseling@gmail.com">RemediesOnlineCounseling@gmail.com</a> Scott Simpson:  Counsellor + Patient Advocate + (former) Triathlete I am a counsellor, patient advocate, and - before I became sick and disabled - a passionate triathlete. Work hard. Train hard. Rest hard. I have been living with HIV since 1998. I was the <a href="https://dignitasinternational.org/2006/08/30/antiretroviral-drugs-keep-hiv-positive-triathlete-on-track-for-world-event-canadian-press/" rel="nofollow" target="_blank">first person living with HIV</a> to compete at the triathlon world championships. Thanks to research and access to medications, HIV is not a problem in my life. I have been living with ME (<a href="https://me-pedia.org/wiki/Myalgic_encephalomyelitis" rel="nofollow" target="_blank">myalgic encephalomyelitis</a>) since 2012, and thanks in part to medical error, it is a big problem in my life. Counseling / Research I first became aware of the ubiquitousness of medical error during a decade of community based research working with the <a href="https://hivprevlab.ca/" rel="nofollow" target="_blank">HIV Prevention Lab</a> at Ryerson University, where I co-authored two research papers on a counseling intervention for people living with HIV, <a href="https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0152762https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0152762" rel="nofollow" target="_blank">here</a> and <a href="https://www.researchgate.net/publication/289366372_Gay_Poz_Sex_A_Sexual_Health_Promotion_Intervention_for_HIV-Positive_Gay_and_Bisexual_Men" rel="nofollow" target="_blank">here</a>.  Patient participants would often report varying degrees of medical neglect, error and harms as part of their counseling sessions. Patient Advocacy I am co-founder of the ME patient advocacy non-profit <a href="https://www.millionsmissingcanada.ca/" rel="nofollow" target="_blank">Millions Missing Canada</a>, and on the Executive Committee of the <a href="https://www.canada.ca/en/institutes-health-research/news/2019/08/government-of-canada-invests-14m-in-biomedical-research-to-improve-the-quality-of-life-of-people-living-with-myalgic-encephalomyelitis.html" rel="nofollow" target="_blank">Interdisciplinary Canadian Collaborative Myalgic Encephalomyelitis Research Network</a>. I am also a patient advisor for <a href="https://www.hqontario.ca/Patient-Partnering/Health-Quality-Ontarios-Patient-Family-and-Public-Advisors-Council" rel="nofollow" target="_blank">Health Quality Ontario’s Patient and Family Advisory Council</a>, and member of <a href="https://www.patientsafetyinstitute.ca/en/About/Programs/PPSC/Pages/default.aspx" rel="nofollow" target="_blank">Patients for Patient Safety Canada</a>. <a href="https://medicalerrorinterviews.podbean.com/" rel="nofollow" target="_blank">Medical Error Interviews</a> podcast and vidcast emerged to give voice to victims, witnesses and participants in this hidden epidemic so we can create change toward a safer health care system. My golden retriever Gladys is a constant source of love and joy. I hope to be well enough again one day to race triathlons again. Or even shovel the snow off the sidewalk.

Mackenzie Doyle: 20 years to get correct diagnosis - mast cell activation syndrome (MCAS)