In this mini-episode special, I speak with NY-based writer and director JB Bruno.  JB is presenting a live performance of A Demon on My Life this June. This online performance will raise funds for #MEAction, a charity and advocacy group focused on myalgic encephalomyelitis (ME), commonly referred to as chronic fatigue syndrome (CFS). The story revolves around Liz and her husband Mark, two dancers who have to navigate the physical and emotional challenges of Liz's ME/CFS. RSVP for the event here: https://bit.ly/2Azywxk

Spoonie Radio

Ep 18.5: JB Bruno

12.6.19   In this episode, Dr. Myhill discusses why nutrition is the number #1 step for treatment of chronic fatigue syndrome and ME. She talks her fight against the PACE authors, critique of the ACUMEN mitochondrial function test, and more...

Ep 18: Dr. Sarah Myhill

11.12.19  Ever thought to crowd source your chronic condition? In episode 17, I sit down with Evan Golub & Nicole Krinick, founders of WANA--a new app that fosters hope, direction, & healing for those with chronic, invisible illness. Hear how a dating app and a diagnosis of Lyme brought these two together to build a community-driven platform to connect patients suffering with otherwise isolating conditions. Download WANA here

Ep 17: Evan & Nicole from WANA

09.16.19  In the long awaited Ep 16, Ken and I take a deep dive into microbiome shifts as primary contributors to the myriad symptoms of CFS and similar conditions. He walks us through how using an AI-tool allows for a deeper understanding of our microbiome, symptoms, & effectiveness of treatments.

Ep 16: Ken Lassesen

11.1.15 In Ep 15, Dr. Younger talks inflammation as it relates to the symptoms of ME/CFS and fibromyalgia. He talks about his research findings, treatment options, testing, and more

Ep 15 Jarred Younger

10.1.15  Dr. Kerr describes his recent mitochondrial findings in functional diseases, ways to protect mitochondria, what ME/CFS patients can learn from Weston Price, and the complex pathogenesis of the illness

Ep 14 Dr. Jonathan Kerr

9.1.15 In Episode 13 I talk to Josh Grant, founder of MENDUS--an online research lab dedicated to patient's exploration of their own health. Inspired by the quantified self movement, Josh aims to garner ME/CFS research interest with this innovative project.

Ep 13: Josh Grant of MENDUS

7.1.15  Dan describes his ME/CFS journey, how to reset HPA axis dysfunction, the wonders of neuroplasticity, and more...

Ep 12 Dan Neuffer

6.1.15 In Ep 11 Toni Bernard talks how to be sick and how to live well with chronic illness. We talk fear and suffering, and how her new book will address the many challenges the chronically ill face every day...

Ep 11: Toni Bernhard

5.1.15 Dr. Bateman and I talk patient autonomy and 5 clinical pearls from years in practice: pacing, emotional resilience, sleep, pain, & treating comorbid conditions

Ep 10: Dr. Lucinda Bateman

4.1.15 Suzanne talks the ME/CFS Biobank, future research, the IOM Report, and more...

Ep 09: Suzanne Vernon

2.4.15 In Part II, Judy and I talk moving forward after XMRV, repurposing drugs, taking a multidisciplinary approach, and how the ME/CFS community can make strides.

Ep 08: Judy Mikovits Part II

2.4.15 Dr. Judy Mikovits talks about her new book Plague, the discovery of gamma retroviruses in ME/CFS, smarter vaccination, scientific censorship, and more

Ep 07: Judy Mikovits Part I

12.17.14 Dr. Nathan talks of his 40 years of being a Chronic Illness Detective, how to approach the complexity of ME/CFS, DHEA, mold, anti-virals, and more...

Ep 06: Dr. Neil Nathan

11.6.14 Dr. Brady talks how chronic infections cause molecular mimicry in the immune system, problems with defining vague conditions like CFS and Fibromyalgia, evidenced-based approaches to viral infections & pain, and more

Ep 05: Dr. David Brady

Spoonie Radio is a Chronic Fatigue Syndrome & Fibromyalgia Podcast highlighting effective treatment strategies as well as insight from clinicians, researchers, & advocates. Each show focuses on evidenced-based, practical information to spread hope and understanding about an otherwise invisible illness. This show is brought to you by Dr. Courtney Craig, recovered CFS patient, clinician, and creator of www.drCourtneyCraig.com

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