With Dan having been a thought leader on the autonomic nervous system and chronic illness for over a decade now, Liz asks him about new research showing a procedure blunting the sympathetic nervous system is helping patients with Long Covid.

In this video, Dan Neuffer, a ME/CFS and Fibromyalgia recovery pioneer from Australia, is back to talk about why some people plateau in their recovery from ME/CFS and how to overcome it.

In part 4 of this interview series, I ask Dan about patterns in people who don’t recover from ME/CFS, Fibromyalgia, POTS and MCS. Are there people for whom recovery simply isn’t possible? We explore mental health impacts on the illness and recovery and predispositions. There were some interesting comments about who does and doesn’t recover more quickly!

In part 3 of this interview series, I ask Dan about people who don’t recover from ME/CFS, Fibromyalgia, POTS, and MCS. Are there people for whom recovery simply isn’t possible? Dan shares some fascinating insights and experiences and has some surprising views on the term ‘mind-body medicine’.

In part 2 of this interview series, we discuss what Dan Neuffer calls ‘the wrong model of health’. We talk about the elusive search for a cure with some surprising views from Dan. We explore how to define partial and full recoveries from ME/CFS, Fibromyalgia, POTS, and MCS and we really dig into some details about Dan’s experience with other people’s recoveries from these conditions.

This interview with Dan Neuffer covers his journey over the last 20 years; his personal experience with ME/CFS, Fibromyalgia, and POTS, his advocacy work, his book and then the creation of his recovery program ANS REWIRE.

Hi Guys, Being bedbound can be a scary place that leaves us feeling helpless. Often we experience sensitivities to any[...]

Explaining the conundrum of how people overcome ME/CFS, Fibromyalgia, POTS, PVFS and MCS when there is no cure. We discuss triggers how people make recovery progress.

In this short video Dan talks about what to do when things go wrong when we are chronically ill with illnesses like Fibromyalgia, ME/CFS, POTS or MCS.

Chronic illness complicates everything in life, including recovery. Dan & Raelan discuss strategies for staying on track for recovery from CFS Fibromyalgia POTS or MCS

Does what triggered your chronic illness like CFS Fibromyalgia POTS or MCS matter? Raelan Agle asks Dan Neuffer in this interview.

Is brain training the answer for recovery from ME/CFS, Fibromyalgia and POTS, and related syndromes? Raelan Agle asks Dan Neuffer in this interview.

In another interview by Raelan Agle, we delve more deeply into the Autonomic Nervous System in the context of recovery from ME/CFS, Fibromyalgia and POTS.

Raelan Agle reached out to her followers about questions they would like to ask Dan Neuffer, and the response was massive. This interview is the result of that response where Dan talks about the recovery process, the pathogenesis of the illness and what answers the many questions about ANS REWIRE.

Coping with invisible illness can be difficult, for sick people as well as those supporting them. Here are some tips to help.

With the onset of the 2020 coronavirus pandemic and economic crisis, I have started a new separate video blog (VLOG) to support all people in the chronic illness community, but especially those people that are experiencing ME/CFS, Fibromyalgia, POTS and related conditions.

What is recovery from fibromyalgia, ME/CFS, POTS or related syndromes? Given that there is no cure, what does "recovery" even mean?

People often think that ME/CFS is just about fatigue. This video is to help educate the wider community and make[...]

Exploring how you make decisions for your CFS/Fibro/POTS recovery may be the most important first step of your recovery to health journey.

My recent health scare has made me reflect about what happens when one day, I will no longer be here. Accordingly, I have reflected on my advocacy efforts for ME/CFS/Fibromyalgia/POTS and come to a big decision that change is warranted after 6 years of effort.

FLASHBACK: It was Sunday morning at around 3.30 am.  As I drifted back into consciousness, I realised I was lying[...]

If you have ME/CFS, Fibromyalgia, POTS or other invisible illness, then chances are you find it frustrating trying to get other people to believe and take your choices seriously, especially family and friends. Here is my advice on how to handle this. For years I have been giving people advice and find myself getting annoyed after all these years when I hear the suffering and frustration that people endure because their choices are not respected.

Getting newly diagnosed with ME/CFS, Fibromyalgia, POTS or similar syndrome can bring up all kinds of emotions. But the decisions we make when we are diagnosed can have both an immediate and ongoing impact on our lives, our health and our chances of recovery. In this video, I talk about my own experience and seeing others experience with this syndrome and how their decisions have impacted their lives. What are your thoughts about the questions I pose in the video? Let's have a discussion and please share this with others experiencing ME/CFS, Fibromyalgia, POTS or related syndrome. I look forward to your thoughts.

A Positive Prognosis For ME/CFS, Fibromyalgia, POTS or MCSPlease note that this article was originally published on Health Rising with[...]

The husband of a former ME/CFS/POTS sufferer describes the impact on the family and how psychotherapy helped the family move forward and for his wife to regain hope and take action to move forward and recover.

Please note that this article was originally published on Health Rising with the title "When Retreat Means Advance: A Recovered[...]

The Key For Fibromyalgia/ME/CFS/POTS/MCS RecoveryDan NeufferAuthor of CFS Unra​​velledAs I write this, I wonder if this is perhaps my most[...]

Frustration that others don't understand what you're going through with ME/CFS, Fibromyalgia and POTS is high, but perhaps you don't understand either!

When we first get sick with ME/CFS or Fibromyalgia, we often get bombarded with a million and one treatment options[...]

A Central Strategy for RecoveryGiven that during my 6+ years of illness, I never met any person either with ME/CFS/Fibromyalgia,[...]

Ever since CFS Unravelled was published, I have been contacted by people diagnosed with Chronic Lyme Disease wondering if they[...]

2 Explosive Realisations About the Suffering with MECFS and FibromyalgiaThe pain was suddenly so severe, that I screamed, “Call an[...]

​“I feel like I am doing all the things I am supposed to do, but I am still not getting[...]

Graded Exercise Therapy for CFS /ME & FMS; Friend or Foe?Most don’t understand WHY graded exercise therapy for CFS /ME/FMS reverses[...]

Alex Howard of OHC Discusses His Experience with Treating ME/CFS EffectivelyAfter I published CFS Unravelled, I have continued to receive[...]

The Loss We Experience When We Have ME/CFS, Fibromyalgia or MCS CLICK THE VIDEO BELOW TO LISTEN TO THE VIDEO[...]

​Everyone fancies offering us their grand advice about exactly how we need to manage, or heal from Fibromyalgia, ME/CFS or[...]

​Cure, Remission, Recovery – Not Just a Play on Words! There is much information out there on how to diagnose[...]

Are You Frustrated?Frustrated with Fibromyalgia? Frustrated with Chronic Fatigue SyndromeFrustrated with Myalgic Encephalomyelitis?Being frustrated with Fibromyalgia or being frustrated with ME/CFS[...]

 David Goding recently interviewed me for an article in Australia Natural Health Magazine.  It's a great article to bring more[...]

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