In My Words

Valerie Davis shares her experience with lung cancer and treatment and we talk about immunotherapy and chemotherapy with A/Prof Clay, an expert on cancer and its treatment. This episode is part of a 4-part miniseries talking about lung cancer treatment; side effects; struggles and mental health; and relationships and support networks. We also talk about support resources that are available to people living with lung cancer. This episode was created using excerpts from our interviews with Valerie Davis and A/Prof Clay. This episode has been kindly supported by Lung Foundation Australia and sponsored by Bristol Myers Squibb.©2021 Bristol-Myers Squibb. Bristol-Myers Squibb Australia Pty Ltd, ABN 33 004 333 322, 4 Nexus Court, Mulgrave, VIC 3170.ONC-AU-2100089. Date of preparation: April 2021

Terri Byrne shares the struggles she has faced living in a region in Australia with limited access to medical treatments and support, her mental health, and what helps her cope. We are also joined by Nicole Parkinson from Lung Foundation Australia, who talked with us about common struggles for people living with lung cancer and what people can do to help them cope. This episode is part of a 4-part miniseries talking about lung cancer treatment; side effects; struggles and mental health; and relationships and support networks. We also talk about support resources that are available to people living with lung cancer. This episode was created using excerpts from our interviews with Terri Byrne and Lung Foundation Support Nurse Nicole Parkinson. This episode has been kindly supported by Lung Foundation Australia and sponsored by Bristol Myers Squibb. 

Valerie Davis shares her experience with immunotherapy side effects and A/Prof Clay talks about what immunotherapy is and how it helps restore the immune system so the body can better fight lung cancer. This episode is part of a 4-part miniseries talking about lung cancer treatment; side effects; struggles and mental health; and relationships and support networks. We also talk about support resources that are available to people living with lung cancer. This episode was created using excerpts from our interviews with Valerie Davis and A/Prof Clay. This episode has been kindly supported by Lung Foundation Australia and sponsored by Bristol Myers Squibb.©2021 Bristol-Myers Squibb. Bristol-Myers Squibb Australia Pty Ltd, ABN 33 004 333 322, 4 Nexus Court, Mulgrave, VIC 3170. ONC-AU-2100090. Date of preparation: April 2021

Michel Itel shares his experience living with lung cancer and relationships and support networks. We are also joined by Nicole Parkinson from Lung Foundation Australia, who provides insights and tips on how people living with lung cancer can manage their relationships. This episode is part of a 4-part miniseries talking about lung cancer treatment; side effects; struggles and mental health; and relationships and support networks. We also talk about support resources that are available to people living with lung cancer. This episode was created using excerpts from our interviews with Michel Itel and Lung Foundation Support Nurse Nicole Parkinson. This episode has been kindly supported by Lung Foundation Australia and sponsored by Bristol Myers Squibb.

Type 2 Diabetes: Managing Your Diabetes, part 2Trudy shares the challenges she faced controlling sugar levels. This episode is part of a 3-part series focusing on a different aspects of managing life with type 2 diabetes and is kindly supported by Diabetes New Zealand and sponsored by Sanofi New Zealand. MAT-NZ-2100010. Date of preparation March 2021. TAPS PP7426.

Type 2 Diabetes: Managing Your Diabetes, part 1Trudy shares how she managed her type 2 diabetes with medication, focusing on insulin. This episode is part of a 3-part series focusing on a different aspects of managing life with type 2 diabetes and is kindly supported by Diabetes New Zealand and sponsored by Sanofi New Zealand. MAT-NZ-2100010. Date of preparation March 2021. TAPS PP7426.

Type 2 Diabetes: Health and LifestyleTrudy shares how type 2 diabetes has impacted health and lifestyle and how she made changes to her life after her diagnosis. This episode is part of a 3-part series focusing on a different aspects of managing life with type 2 diabetes and is kindly supported by Diabetes New Zealand and sponsored by Sanofi New Zealand. MAT-NZ-2100010. Date of preparation March 2021. TAPS PP7426.

This episode has been translated for a Spanish-speaking audience. Support for this episode comes from Novo Nordisk. Please click here for prescribing information. Cathy shares what it is like to live with Glanzmann's thrombasthenia and how a treatment has helped her manage her condition. Some topics discussed in this podcast may not be appropriate for children.

Multiple sclerosis, or MS, is a topic we've covered in the past. But, everyone's experience with the condition is unique. In our next two episodes, we hear from Astrid, an MS advocate who has been living with the condition for over six years. In this episode, we hear her diagnosis story, as she provides some helpful advice she's learned over the years. We also hear from Dr. John Parratt, a neurologist at Royal North Shore Hospital in Sydney, Australia, who provides a clinical perspective and advice from his years treating MS patients. This episode is kindly supported by MS Australia and is sponsored by Roche Australia (Sydney). Material number EC-AU-9369, prepared Apr2020. Episode References:  MS Australia. Understanding Multiple Sclerosis – An Introductory Guide. Available at: https://www.msaustralia.org.au/publications/understanding-ms-introductory-guide Chwastiak LA, Ehde DM. Psychiatric issues in multiple sclerosis. Psychiatr Clin North Am. 2007;30(4):803–817. 

Managing a chronic condition like multiple sclerosis can be complicated. In the second part of Astrid’s story, we hear about her experiences with disease symptoms and complications, treatment, supportive therapies, lifestyle changes, and support networks, all of which play a part in helping her and others with MS live well. We’ll again hear from Dr. John Parratt about what it’s like managing the condition, including explanations of treatment types and strategies for getting the support you need as a person living with MS.  This episode is kindly supported by MS Australia and is sponsored by Roche Australia (Sydney). Material number EC-AU-9437, prepared Apr2020. Episode References: MS Australia. Symptoms. Available at: https://www.msaustralia.org.au/about-ms/symptoms. Accessed April 2020. MedicineNet. Medical Definition of Proprioception. Available at: https://www.medicinenet.com/script/main/art.asp?articlekey=6393. Accessed April 2020. International Association for the study of pain. IASP Terminology – Neuropathic pain. Available at: https://www.iasp-pain.org/terminology?navItemNumber=576#Neuropathicpain. Accessed April 2020. WebMD. What Are the Side Effects of Pain Medication? Available at: https://www.webmd.com/pain-management/pain-medication-side-effects#2. Accessed April 2020. MS Australia. Medications & Treatments. Available at: https://www.msaustralia.org.au/about-ms/medications-treatments. Accessed April 2020. MS Australia. Understanding Multiple Sclerosis – An Introductory Guide. Available at: https://www.msaustralia.org.au/publications/understanding-ms-introductory-guide. Accessed March 2020. MS Australia. Diet & Nutrition. Available at: https://www.msaustralia.org.au/wellbeing-ms/diet-nutrition. Accessed April 2020. Exercise is Medicine Australia Factsheet. Available at: http://exerciseismedicine.com.au/wp-content/uploads/2019/12/Factsheet-MS-BRIEF-VERSION-2014.pdf. Accessed April 2020. Chwastiak LA, Ehde DM. Psychiatric issues in multiple sclerosis. Psychiatr Clin North Am. 2007;30(4):803–817. MS Research Australia. MS Treatments. Available at: https://msra.org.au/treatments/. Accessed April 2020. Broadley SA, Barnett MH, Boggild M, Brew BJ, Butzkueven H, Heard R, Hodgkinson S, Kermode AG, Lechner-Scott J, Macdonell RA, Marriott M, Mason DF, Parratt J, Reddel SW, Shaw CP, Slee M, Spies JM, Taylor BV, Carroll WM, Kilpatrick TJ, King J, McCombe PA, Pollard JD, Willoughby E. A new era in the treatment of multiple sclerosis. Medical Journal of Australia 2015; 203(3): 139-141. Clanet MC, Wolinsky JS, Ashton RJ, Hartung HP, Reingold SC. Risk evaluation and monitoring in multiple sclerosis therapeutics. Mult Scler 2014; 20(10): 1306-1311. Halabchi F, Alizadeh Z, Sahraian MA, Abolhasani M. Exercise prescription for patients with multiple sclerosis; potential benefits and practical recommendations. BMC Neurol 2017; 17(1): 185. Klotz L, Havla J, Schwab N, Hohlfeld R, Barnett M, Reddel S, Wiendl H. Risks and risk management in modern multiple sclerosis immunotherapeutic treatment. Ther Adv Neurol Disord 2019; 12: 1756286419836571. Mokhtarzade M, Ranjbar R, Majdinasab N, Patel D, Molanouri Shamsi M. Effect of aerobic interval training on serum IL-10, TNFalpha, and adipokines levels in women with multiple sclerosis: possible relations with fatigue and quality of life. Endocrine 2017; 57(2): 262-271. Tintore M, Vidal-Jordana A, Sastre-Garriga J. Treatment of multiple sclerosis - success from bench to bedside. Nat Rev Neurol 2019; 15(1): 53-58. Zimmer P, Bloch W, Schenk A, Oberste M, Riedel S, Kool J, Langdon D, Dalgas U, Kesselring J, Bansi J. High-intensity interval exercise improves cognitive performance and reduces matrix metalloproteinases-2 serum levels in persons with multiple sclerosis: A randomized controlled trial. Mult Scler 2018; 24(12): 1635-1644.

Support for this episode comes from Novo Nordisk. Please click here for prescribing information. Cathy shares what it is like to live with Glanzmann's thrombasthenia and how a treatment has helped her manage her condition. Some topics discussed in this podcast may not be appropriate for children.

Luka goes on an adventure to learn how vernal keratoconjunctivitis affects the eyes and what he can do to manage it.

Support for this episode comes from Novo Nordisk. Vaughn shares what it was like growing up with hemophilia and how medicine has helped him manage his condition. You can also watch a video to learn more about the Ripley family.

Robbie takes a trip to the kidneys to learn more about how the kidneys work, what happens when they are damaged, and what treatments are available.

Daron shares the little things he does to help keep his blood sugars under control, while maintaining his university workload to avoid burnout. Nurse Joanna Naylor talks about the importance of informing your employers and co-workers about your condition, and of having a job you’re passionate about. Finally, Daron offers tips for diabetes management while travelling. This episode is part of a 5-part series focusing on a different aspects of managing life with type 1 or type 2 diabetes and is kindly supported by Diabetes New Zealand and sponsored by Sanofi New Zealand. Disclaimer: These episodes are intended for a non-US audience. Units of measurement for blood glucose are referred to in mmol/L rather than the standard US mg/dL.

Daron and diabetes nurse, Joanna Naylor, discuss healthy relationships and the importance of educating family, friends, and flatmates on diabetes so they can provide extra support. They also talk about the transition period from parents managing your blood sugars to taking care of yourself. This episode is part of a 5-part series focusing on a different aspects of managing life with type 1 or type 2 diabetes and is kindly supported by Diabetes New Zealand and sponsored by Sanofi New Zealand. Disclaimer: These episodes are intended for a non-US audience. Units of measurement for blood glucose are referred to in mmol/L rather than the standard US mg/dL.

Cody and Lexi learn about their father's lung cancer - how lung cancer affects the body, common symptoms, and how lung cancer is treated. 

Daron shares how type 1 diabetes has impacted his exercise routines and how he keeps a positive mindset. Diabetes nurse, Joanna Naylor, explains how working with a diabetes practitioner can help improve mental health and overall blood sugar management. Daron and Joanna also discuss the potential dangers of drinking alcohol as a person living with T1D. This episode is part of a 5-part series focusing on a different aspects of managing life with type 1 or type 2 diabetes and is kindly supported by Diabetes New Zealand and sponsored by Sanofi New Zealand. Disclaimer: These episodes are intended for a non-US audience. Units of measurement for blood glucose are referred to in mmol/L rather than the standard US mg/dL.

In his words, Karl shares his experience of being diagnosed with type 2 diabetes in his 30’s and how it has changed his life. Doctor Murphy debunks common myths and offers advice on successful T2D management. This episode is part of a 5-part series focusing on a different aspects of managing life with type 1 or type 2 diabetes and is kindly supported by Diabetes New Zealand and sponsored by Sanofi New Zealand. Disclaimer: These episodes are intended for a non-US audience. Units of measurement for blood glucose are referred to in mmol/L rather than the standard US mg/dL.

Daron tells us the story of his diagnosis with type 1 diabetes at age 12 and how he’s learned to manage life after diagnosis. Diabetes nurse, Joanna Naylor, shares her clinical perspective and debunks some of the misconceptions and challenges surrounding living with the condition. This episode is part of a 5-part series focusing on a different aspects of managing life with type 1 or type 2 diabetes and is kindly supported by Diabetes New Zealand and sponsored by Sanofi New Zealand. Disclaimer: These episodes are intended for a non-US audience. Units of measurement for blood glucose are referred to in mmol/L rather than the standard U.S. mg/dL.

Jenny aprende cómo el asma afecta los pulmones, cómo manejar los ataques de asma, y qué médicas pueden ayudar a controlar el asma.

Samantha and her mom learn what to expect during a clinical trial, what permission is needed, and how participating in a clinical trial can help others.

Today we’re talking with Art Director Marcelo Ferreira about the work he does, the impact of bringing the stories of real kids and real families to life, and the evolution of creating comic books at Jumo Health.

Maggie learns about what happens before, during, and after an operation, and the surgical team who will be taking care of her.

T1D affects everyone differently, but often the 24/7 burden of diabetes management is not fully understood. Today we’re talking with two of our very own employees here at Jumo Health about their everyday reality of living with Type 1 diabetes.

Amy learns how ulcerative colitis affects your digestive system, what symptoms to expect, how to avoid triggers, and what treatment options are available to reduce flare-ups.

Jumo and the JED Foundation are teaming up to create more mental health resources for teens and young adults. We spoke with JED Foundation's executive director, John MacPhee, and psychiatrist, Dr. Victor Schwartz about what they are doing to expand the conversation, and about the resources available to help young people with mental health issues.

Tim learns how type 1 diabetes works in the body, what symptoms to expect and how to manage his blood glucose levels with insulin.

Through Dr. Dave, we learn the story of Alexandra, who shares her experiences living with cystic fibrosis and how her palliative care team made treatments easier for her and her family in the comfort of their own home.

Cody learns how cancer affects the body and how chemotherapy treatment works.

Thomas and Bridget learn how metastatic breast cancer affects the body, and how chemotherapy, targeted biological therapy, hormone therapy, radiation therapy, surgery, palliative care, or clinical trials can help.

Learn how each member of your health care team takes care of you before, during, and after your hospital stay.

Corey learns about how the heart works, different types of congenital heart defects, and how heart defect symptoms are treated.

Medical procedures may sound scary. The Medikidz help Melissa conquer her fears by taking her on a journey through the human body to understand how PICC lines work and how to keep it clean and dry to avoid infection.

Jett learns how stem cells work and what happens before and after an autologous or allogeneic transplant.

Julia a high schooler with epilepsy is going off to college. She meets Brian, a college kid who has conquered this fear before. He shares his experiences of transitioning from a pediatrician to a new epilepsy team geared toward adults, and becoming more independent in epilepsy management.

Duke learns more about his appendix, appendicitis, and appendectomy procedure.

Vincent learns more about how attention deficit hyperactivity disorder works in the brain and how ADHD is treated.

The Medikidz take Dean on a journey to the bone marrow to learn more about how blood cells work, symptoms and treatment of chronic myeloid leukemia (CML), possible side effects, and how to find more support.

Jenny learns more about how the ovaries work, how ovarian cancer affects the body, and how ovarian cancer is treated.

Charlie learns how leukemia is diagnosed, what it does to the body, and what to expect with leukemia treatment. 

Melanie learns more about how concussions affect the brain and concussion recovery.

Rafeeq learns how MRIs work, and what happens during an MRI.

Kevin learns how blood transfusions work, when they are needed and how blood donors are chosen.

The Medikidz take Lucas on a journey through the bladder to learn more about how clean intermittent catheterization (CIC) works in boys, how to use a catheter properly, and how to avoid infections.

Kerianne, diagnosed with Crohn's disease as a teen, shares the ups and downs of her journey, incuding the side effects of medications, how her diet changed after surgery, what it was like living with a chronic illness in high school, and advice for other young adults living with Crohn's disease. Learn more about Crohn's disease and another patient's story in our Understanding Crohn’s Disease comic book.

The Medikidz take Jackie on a journey through the bladder to learn more about how clean intermittent catheterization (CIC) works in girls, how to use a catheter properly, and how to avoid infections.

Chris takes a journey through the human body to learn more about his adrenal glands, hormone imbalance, and the symptoms and treatment of congenital adrenal hyperplasia (CAH).

Continuing our conversation with MS advocate Adriana, MS nurse Belinda Bardsley, and neurologist Dr. Boggild, we talk about what treatments and supportive therapies are available to people with MS and how MS treatment decisions are made. Listen to Part 2 of Adriana's story Watch a day in the life of Adriana in her In My Shoes video here. This episode has kindly been supported by MS Australia and sponsored by Roche Australia, material number 37562681 and prepared in May 2018.

Adriana shares how MS has impacted her career and lifestyle. MS nurse Belinda Bardsley, and neurologist Dr. Boggild share their expertise on maintaining a career and making healthy lifestyle choices after a diagnosis of MS. Listen to Part 3 of Adriana's story. Watch a day in the life of Adriana in her In My Shoes video here. This episode has kindly been supported by MS Australia and sponsored by Roche Australia, material number 37562681 and prepared in May 2018.

Adriana talks to us about the ups and downs she faces as a parent living with MS. MS nurse Belinda Bardsley, and neurologist Dr. Boggild share their professional advice on family management. Listen to Part 4 of Adriana's story. Watch a day in the life of Adriana in her In My Shoes video here. This episode has kindly been supported by MS Australia and sponsored by Roche Australia, material number 37562681 and prepared in May 2018.