Jonathan sits down with Dr. Tommy Martin: a doctor of Internal Medicine and Pediatrics, a husband, and a father to Oliver, who has Lamb Shaffer Syndrome. This episode has been a year in the making!  Jonathan talks to Tommy about fatherhood, being a caregiver to his son, Lamb Shaffer Syndrome, being a physician, and everything in between.   

Dr. Tommy is one of Jonathan's role models, and he is so excited to have this opportunity!   

Dr. Tommy's Social Media:    

Instagram: dr.tommymartin  

TikTok: dr.tommymartin  

YouTube: https://www.youtube.com/c/TommyMartinMD/

In today’s episode, Jonathan sits down with  Ella Balasa,  a patient advocate and a person living with Cystic Fibrosis. She shares her experience with her disease and the opportunities she has had as a patient advocate. She is insightful, resourceful, and a champion in the face of adversity.

To learn more about Cystic Fibrosis, visit: https://www.cff.org/

To learn about Ella and her work, visit: www.ellabalasa.com

After an extended break, the 1 of 20 Podcast is back to school!  Jonathan sits down with “The Northern Nerd” Mr. Dalton Hessel, a second-grade teacher from Wisconsin, and discusses all things back to school. This time of year can be exciting but for students who have challenges and are differently abled, it can be a nightmare. Tune in to see how Dalton fosters a safe inclusive environment for his students.   

Dalton's Social Media:  

Jonathan sits down with Madison Bopp, who suffers from Psoriasis. They have an open conversation about the disease and her day-to-day with it. 

Jonathan sits down with Aubrey, a Girl Scout who has made her Gold Award all about Rare Diseases. Tune into see how she is making a difference in the rare community!

On the Season 2 premiere of the 1 of 20 Podcast- Jonathan sits down with Whitney Frost, who has two children with INAD.

Infantile neuroaxonal dystrophy (INAD) is a rare inherited neurological disorder. It affects axons, the part of a nerve cell that carries messages from the brain to other parts of the body, and causes progressive loss of vision, muscular control, and mental skills.

Whitney has over 1.3 million followers on TikTok, where she shares her life with her family and two young children that have INAD. 

Tune in to Spotify, Google Podcasts, or wherever you get your podcasts to listen to Jonathan and Whitney discuss the ups and downs of chronic illness, having a platform, and living and caring with those who have rare diseases.

In this abbreviated episode of the 1 of 20 podcast, Jonathan takes the time to reflect on life as a college graduate. Tune in, and stay tuned for Season 2 in September!

In this episode, Jonathan and special guest Sydney Reynolds, talk about mental health during the global pandemic. They reminisce on the ups and downs, their daily struggles, and their lifestyle during these tough times.

In this episode, Jonathan and special guest Georgina Lloyd talk about the differences between Diabetes and Hypoglycemia. They reminisce on the ups and downs, their daily struggles, and their lifestyle. Please tune in on YouTube, Spotify, Google Podcasts and wherever you get your podcasts!  #chronicillness​ #rare​ #raredisease​ #rarediseaseawareness​ #healthyliving​ #cleaneating​ #fastfood​ #recovery​ #podcasts​ #podcastersofyoutube​ #content​ #contentcreation​ #podernfamily​ #life​ #newepisode​ #entertainment​ #business​ #follow​ #movies​ #rap​ #funny​ #live​ #inspiration​ #sports​ #instagram​ #film​ #podcastlove​ #horror​ #media​ #podcastinglife​ #instagood​ #podcastaddict​ #podcastsofinstagram​ #podcasthost​ #coronavirus​ #quarantine​ #news​ #explorepage​ #googlepodcasts​ #mentalhealth​ #artist​ #diabetes​ #diabetic

On this episode, Jonathan sits down in the studio and talks all about his safe foods. He explores nutrition labels and has a candid conversation about his relationship with food and healthy eating.