Join our team in a discussion about diagnosis and treatment of glomerulonephritis, a common cause of kidney failure. We explore new treatment options and ways to engage patients in conversations about these options. Additionally, we unpack how to diagnose and monitor glomerulonephritis. This discussion also includes challenges faced both by patients and providers with regard to glomerulonephritis, especially for women of child-bearing age.

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The management of patients living with kidney disease is evolving as the complexity of patient care evolves. Join us as we discuss the team of clinicians who are involved in the care of patients with kidney disease, including nephrologists and advanced practice providers (APPs) - advanced practice registered nurses (APRNs) and physician assistants (PAs). This episode will review the roles of each provider type and what each brings to the team as well as the patients. It will also highlight the strengths of team-based care as well as what patients and their families can expect from an APP during clinic visits, hospitalizations, transplant workups, and on dialysis units. 

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Many people start the year full of hope and ready to start anew. Join our team in a discussion about the best times to implement new goals relative to CKD. We also explore home dialysis modalities and ways to engage patients in conversations about this option. Additionally, we unpack how and when to implement exercise programs and include tips on tackling social isolation. We hope you enjoy this podcast as you continue in this new year. 

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Join us for a robust discussion surrounding the ever-growing field of vitamins and supplements.  This episode dives into the indications and contraindications for people with all stages of chronic kidney disease, including those on dialysis as well as those who have had a transplant.  The panelists will also review the potential drug interactions and side effect profiles of the most commonly inquired about supplements.  Which vitamins may be appropriate and when will be included in this episode as well.   

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Having a chronic illness can be difficult for anyone. Patients with Kidney disease have to restrict their diet and also balance out restrictions associated with other medical illnesses. Considering diet and fluid restrictions while planning family meals can be physically and emotionally taxing. In this episode, you will gain insight into the patient experience of planning around the holidays and professional teams knowledge in providing the best education for patients and the best holiday outcomes.

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Hypertensive disorders of pregnancy impact many pregnancies and are associated with significant maternal and fetal morbidity and even mortality. In this episode of the kidney commute, we are joined by a maternal fetal medicine (high risk obstetrics) expert, as well as a nephrologist, pharmacist, and patient to discuss these disorders. Patients with kidney disease are at elevated risk of developing hypertensive disorders of pregnancy and it is important that members of the kidney community be able to recognize and treat these conditions, as well as to know when to refer for more help.

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The National Kidney Foundation is excited bring to you an important conversation about awareness, sensitivity and understanding of the LGBTQ+ community. In this episode, we will discuss how the use of appropriate intake forms, use of pronouns and having open conversations can create an inclusive healthcare environment and create a shared decision making environment. Participants will receive education on what considerations should be made when exploring gender affirmation hormone therapy or surgery in their patient population. Gender-affirming hormone therapy can be taken as pills, patches, gels, or by injection.  Hormone therapy can be given alone or with preparation for gender-affirming surgery.  Want to learn more? Hop in and enjoy this episode of the Kidney Commute!

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In this episode, we discuss the process of working towards a kidney transplant. Exploring the steps from the perspective of the patient and the different members of the healthcare team. We find out when a referral for transplant is appropriate, as well as the testing required before a patient is deemed a good candidate for a kidney transplant.

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Transplant is the preferred modality for many people with end-stage renal disease. There are approximately 100,000 people waiting for a kidney transplant, with wait times exceeding 10 years in some regions. Join us on this ride as we discuss ways to find living donors as an alternative to a deceased donor kidney transplant. We will discuss the experience of living donors through the work up phase, the surgical phase, and throughout the emotional and physical healing phase of this life-saving gift.

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Sexual dysfunction (SD) is incredibly common in patients with kidney disease. In women, SD is classified as sexual interest/arousal disorder, orgasmic disorder, and genitopelvic pain/penetration disorder. For men, SD is classified as erectile disorder, hypoactive disorder, premature ejaculation, and delayed ejaculation. Studies have shown rates of SD as high as 92% of women with CKD and 70-85% of men, with increasing rates as kidney disease progresses. In this episode, our interdisciplinary team discusses why SD is so prevalent in patients with CKD, how it is discussed and diagnosed, some treatment options, and our thoughts on how to improve communication about this important but often neglected aspect of overall health.

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Access our resources here:

“Sexuality and Kidney Disease” from NKF Website: https://www.kidney.org/atoz/content/sexuality

Rosy App

https://meetrosy.com/