Dan Neuffer answers questions posted by the ME/CFS community in this interview
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.
Invisible Illness – 7 Ways To Get Past The Injustices and Challenges!
Coping with invisible illness can be difficult, for sick people as well as those supporting them. Here are some tips to help.
Support During Crisis
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 or POTS?
What is recovery from fibromyalgia, ME/CFS, POTS or related syndromes? Given that there is no cure, what does "recovery" even mean?
Making Decisions and Taking Actions for Recovery from Fibromyalgia, ME/CFS and POTS
Exploring how you make decisions for your CFS/Fibro/POTS recovery may be the most important first step of your recovery to health journey.
After 6 years it’s time I make a change
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.
Lessons from my life-saving surgery that might save your life!
FLASHBACK: It was Sunday morning at around 3.30 am. As I drifted back into consciousness, I realised I was lying[...]
3 Problems Chronically Ill people can avoid by STOPPING this
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.
Diagnosis of ME/CFS Fibromyalgia POTS – How acceptance could impact your life
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.
How Recovery From ME/CFS and POTS Was Enabled By Psychotherapy For The Family
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.
Is this powerful instinct our body’s message to help us treat & overcome MECFS, Fibromyalgia & POTS?
Please note that this article was originally published on Health Rising with the title "When Retreat Means Advance: A Recovered[...]
Neuroplasticity & Recovery From Fibromyalgia and MECFS
The Key For Fibromyalgia/ME/CFS RecoveryDan NeufferAuthor of CFS UnravelledAs I write this, I wonder if this is perhaps my most[...]
Others don’t understand what you’re going through with ME/CFS, Fibromyalgia or POTS, but do you?
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!
Choosing the Right Fibromyalgia Treatments or ME/CFS Treatments for your Recovery Action Plan
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 Recovery from Fibromyalgia & MECFS
A Central Strategy for RecoveryGiven that during my 6+ years of illness, I never met any person either with ME/CFS/Fibromyalgia,[...]
2 Explosive Realisations About the Suffering with MECFS and Fibromyalgia
2 Explosive Realisations About the Suffering with MECFS and FibromyalgiaThe pain was suddenly so severe, that I screamed, “Call an[...]
Why are others recovering from ME/CFS and Fibromyalgia and not I?
“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 and FMS Friend or Foe
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 ME-CFS & Fibromyalgia
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 MECFS, Fibromyaliga & MCS
The Loss We Experience When We Have ME/CFS, Fibromyalgia or MCS CLICK THE VIDEO BELOW TO LISTEN TO THE VIDEO[...]
3 Crucial Components for Recovery from Fibromyalgia Syndrome, ME/CFS and Multiple Chemical Sensitivities
Everyone fancies offering us their grand advice about exactly how we need to manage, or heal from Fibromyalgia, ME/CFS or[...]
The truth about cures for fibromyalgia, ME/CFS & POTS and what recovery means
Cure, Remission, Recovery – Not Just a Play on Words! There is much information out there on how to diagnose[...]
Can you Tranform Feeling Frustrated with Fibromyalgia or ME/CFS into Opportunity?
Are You Frustrated?Frustrated with Fibromyalgia? Frustrated with Chronic Fatigue SyndromeFrustrated with Myalgic Encephalomyelitis?Being frustrated with Fibromyalgia or being frustrated with ME/CFS[...]
My talk about Hope for Fibromyalgia Recovery & Chronic Fatigue Syndrome Recovery – VIDEO
Talk About Hope for Fibromyalgia Recovery & CFS RecoveryRecently I was invited to speak at a Gold Coast CFS/FM Support[...]