Travel with us as we look back at a powerful season of Warrior stories. We’ll touch on some of the highlights, lessons learned, and memorable moments of the first-ever season of the Nephrotic Syndrome Foundation Podcast. Listen all the way through to hear the exciting new direction we’ll head as season 2 of the podcast kicks off this August.

Gratitude and vulnerability don’t usually come easily. But when Mikaela was diagnosed at 16, she didn’t waste any time exemplifying both qualities while still in the hospital. Listen in as she shares about attitude, meds, horseback riding, and a path towards helping others.

It takes most of us a lifetime to gain the wisdom, and insight Jasmine has earned in her early 20’s. Despite a diagnosis of Nephrotic Syndrome at 18, she courageously pursues her passion for professionally performing in the arts. In this upbeat but transparent conversation she shares about being grateful, choosing acceptance, and pursuing a stress-free, happy lifestyle.

No two journeys are alike—and this is particularly true in the world of Nephrotic Syndrome. Despite being put on several commonly used medications, Nicki did not find hope or healing until she had a mental shift and started working with a team of doctors that looked at all aspects of her health. In this episode, Nicki shares her story about the connectedness of health and lifestyle and the incredible power of a supportive community.

Sometimes one small kernel of truth can make all the difference in a person’s daily experience. Dr. Ryan Lazarus understands this personally and professionally. Battling chronic illness from the age of 18, his struggles became the fuel to discover the best functional solutions for each of his patients. In this episode, he opens up the world of integrative medicine and how it can significantly impact those challenged with chronic illness.

Facing a life of chronic illness with grace, determination, and courage might seem like an impossible feat. But Natalie Robinson is here to prove otherwise. In this episode, she candidly shares about community, accomplishments, and the personal choices she makes as she navigates Nephrotic Syndrome.

At times in life, we come across people that can’t help but inspire. They embolden us to face challenges with a new perspective and fresh attitude. Cynthia Niemeyer is one of those people. From the early age of 2, she has fought for her health. Facing several diagnoses—including minimal change disease—she was fondly nicknamed, “Miss Perky” by those who knew her best. In this episode, you’ll hear about the foundation of a healthy family, the importance of finding something you love, and the power of chasing your dreams.

At the young age of six, Wilson and his family were thrust into a world they knew nothing about. A diagnosis of Minimal Change Disease turned their “normal” into “navigating the unknown.” In this episode, Andi shares their story of understanding, courage, and connecting with others.

An inspiring story, a much-needed word of encouragement, or a well-placed bit of advice can make all the difference in a difficult journey. And sometimes, all it takes is knowing that you’re not alone. Hear from hosts Andi Callaway & Jeremy Bedig on the inspiration behind it all, the ups and downs of getting started and where they plan to go from here! Andi is the Founder and the President of the Nephrotic Syndrome Foundation and has a teenage son diagnosed with Minimal Change Disease (MCD) at age 6. Jeremy is a two time kidney transplant recipient and professional soccer coach initially diagnosed with Focal Segmental Glomerulosclerosis (FSGS) at age 14.