The fifth and final article in a series attempting to explain the science behind fairly common topics and exploring how they relate to ME/CFS. This time the topic is the nervous system – by Andrew Gladman. The nervous system, specifically the autonomic nervous system, is frequently discussed in relation to ME/CFS, with quite a plethora of research being targeted in this
ContinueYour Chance to Endorse Tom Kindlon’s Nomination in the WEGO Health Activist Awards
Tom Kindlon has been nominated in two categories for his herculean efforts with regard to health activism on the internet and in particular his work in disseminating the reality of the PACE Trial and GET/CBT as ‘effective’ treatments for ME/CFS. By Firestormm. The other day, I happened to notice a link posted on the Phoenix Rising Facebook page to the
ContinueWriting as Therapy: My ME/CFS Story
Jody Smith reflects on how vital she has found the slow return of her writing ability – how it has helped with the expression of feelings and experiences, contributed to reestablishing a sense of self, and has proved such an important and productive means of social interaction… In my life before ME/CFS, I did a lot of writing. I kept
ContinueLyme on my mind
Astrid13 recalls the alarming mental confusion associated with her life of chronic illness and explains how her own search for answers may finally be yielding results – though she still has a long road to travel… In 2006, following a miscarriage, I began to suffer the most horrible cognitive decline. A D&C had been performed under general anesthesia and after
ContinueLiving the Half-life of ME/CFS
Jody Smith relates how tiny victories helped her regain a life despite her limitations. What is it about situations that are unfamiliar that make our brains feel lumpy and our bodies feel like they are moving (or trying to) in another dimension? When I was at my sickest with ME/CFS, this wasn’t much of a problem, because I was spending
ContinueAm I “Allergic to Life”?
Janis Bell (JanisB) reviews her personal journey of chronic illness after being inspired by a new article written by Jill Neimark and appearing online today in Discover magazine. It highlights the work of Dr Claudia Miller (pictured) and her theories relating to extreme chemical sensitivity and toxicants, a condition she terms, Toxicant-induced Loss of Tolerance or TILT. By the time
ContinueDeath Contract? ME/CFS Experts and Advocates Unite to Oppose US ‘Case Definition’ Contract
Mark Berry asks why the US HHS contract with the Institute of Medicine (IOM) to re-define ME/CFS has provoked such an unprecedented storm of protest, and explores the reactions of patients, organizations, experts and bloggers to the so-called ‘Death Contract’. On September 23rd, 2013, the US Department Of Health and Human Services (HHS) made an announcement that was to send
ContinueThe Nightmare Scenario – IOM Case Definition Contract Terrifies ME/CFS Advocates
Gabby (Nielk) presents a nightmare vision of what the future might hold for ME/CFS patients in the US, if the Institute of Medicine (IOM) contract to redefine ME/CFS turns out as badly as many patients and advocates fear. Imagine that you magically wake up to a day in October of 2015. Unfortunately you are still ill with ME/CFS and it’s
ContinueIn Brief: The Cardiovascular System and ME
The fourth in a series of short articles attempting to explain the science behind fairly common topics and exploring how they relate to ME. This time the topic is the Cardiovascular System – by Andrew Gladman. The cardiovascular system is not one that is commonly discussed in relation to ME, and yet it is an area that research has shown displays
ContinueCanary in a Coalmine – Exclusive interview and film trailer help launch Kickstarter campaign!
Filmmaker Jennifer Brea launches the Kickstarter campaign today with the trailer of her forthcoming documentary Canary in a Coal Mine – a film that will help change the face of ME. Interview and article by Russell Fleming (Firestormm). When did you first get sick and why did you decide to make a film? “It started with the worst flu of
ContinueIn Brief: Mitochondria and ME
The third in a series of short articles attempting to explain the science behind fairly common topics and exploring how they relate to ME. This time the topic is Mitochondria – by Andrew Gladman. Over the years it is fairly safe to say that finding consistent physiological abnormalities in ME has proven difficult for researchers, and that this has likely reinforced
ContinueHow Do You Handle Autumn?
Jody Smith explains how autumn sends her body into hibernation mode, and it’s time to slow down – or else. I read recently that the term “autumn” is predominantly used in the U.K. “Fall” is more commonly used in the U.S. I’m Canadian, though, so I guess I can use either one. And I choose “autumn” simply because it causes
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