THE NICEGUIDELINES BLOG

Doctor Speedy and ME in search of medical honesty

Thursday, December 22, 2011

MRC misuse ME funding for other diseases

Medical Research Council announces ME/CFS research projects worth £1.6m: "Summary:

Researchers will analyse the immune systems of more than 500 patients with primary Sjögren syndrome"

Read more>>


See also: The main characteristic of ME is an abnormally delayed muscle recovery after doing trivial things, if you don't have that, you don't have ME

See also: Harvard Medical School: EEG spectral coherence data distinguish chronic fatigue syndrome patients from healthy controls and depressed patients 
See also: The putative agent of ME/CFS can be transferred to monkeys 
See also: Almost 5% of ME/CFS patients contracted ME/CFS from a blood transfusion
See also: Cerebrospinal fluid profiles can differentiate between Lyme disease, ME/CFS and healthy controls
See also: The main characteristic of ME is an abnormally delayed muscle recovery after doing trivial things, if you don't have that, you don't have ME
Posted by Dr Speedy at 3:41 AM
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Labels: CHRONIC DISEASE, Coping, GOBSART, Health, LIFE, ME, ME/CFS, Psycho blah blah, RESEARCH, Science

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# The main characteristic of ME is an abnormally delayed muscle recovery after doing trivial things, if you don't have that, you don't have ME
"Plenty of people are still dying of diseases which other people do not believe." (Dr. M.N.C. Dukes).
Dr SpeedyCBT and GET for ME: "There is no nonsense so gross that society will not, at some time, make a doctrine of it and defend it with every weapon of communal stupidity."

Robertson Davies

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THE NICEGUIDELINES BLOG VERSUS THE NICEGUIDELINES

These are NOT the NICEGuidelines. This is "The NICEGUIDELINES BLOG." What are the differences:

The NICE Guidelines are biased publications based on the GOBSART (Good Old Boys Sitting Around a Table) approach.

This Blog however is not only evidence based but also uses critical reading to judge papers and articles. I also use common sense and listen to others. And finally I read both psychiatric and medical evidence and opinions from around the world to come to a conclusion.

I’m not sponsored by anybody or paid by whatever company as seems to be the norm with many psycho people who publish the same article almost on a weekly base.

So if you value an opinion, formed as a result of participating in many ME activities, for example being bed bound for years, you have come to the right BLOG. All these activities have allowed me to form an opinion as a Doctor and as a Patient. And that is important as the voice of the latter is discarded by many including NICE.

If you don’t read this blog, you will miss out on “accredited” medical education. If you do read it, you may actually become a doctor who doesn’t stop thinking or forgets to ask critical questions. Many good things, including satisfied patients are at your command.

So, if you arrived here for the straightforward GOBSART approach, I will disappoint you. If you are interested in forming your own opinion about ME, and other interesting things, read on!

About Dr. Speedy.

I am a Family Physician or GP as it is called in Australia or the UK. I am also an ME patient unfortunately. Bedbound that is. So at the moment I’m in private practice so to speak. I’ve got only one patient, ME, or is it me?

I graduated as a doctor a long time ago, and I am the founder and editor of The NICEGUIDELINES BLOG, an internet based ME BLOG that is devoted to critical reading and cheering you or ME up.

I have the following conflict of interest: I would like to get better and see that the wasting of public money on CBT (talk therapy for a neurological disease, really helpful) and other silly therapies for ME stops, and will be used in better ways.

My goal has always been to help, and if possible, cure patients. With this disease you will soon find out that many psychiatrists and psychologists are only in it to make money and get their name in the spotlight. And what happens to and with the patients is irrelevant.

I stand to benefit both mentally, physically and also financially if this silliness would stop, and I would get my health back, and I can go back to work and have a normal life again. Please evaluate my postings with this in mind! And remember, there are also (lots of) psychiatrists and psychologists who haven’t switched their brain off.

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Important Sites to Check Out

  • 2010 Revised Canadian Myalgic Encephalomyelitis Chronic Fatigue Syndrome criteria.pdf
  • Article: The PACE Trial Invalidates the Use of Cognitive Behavioral and Graded Exercise Therapy in Myalgic Encephalomyelitis/ Chronic Fatigue Syndrome: A Review
  • Biomedical ME/CFIDS
  • CFS Central
  • CFS Patient Advocate
  • Cinder Bridge
  • Dr Simon Wessely, no not that one
  • Follow ME in Denmark
  • GP revalidation !!!
  • Glasbergen Cartoons
  • HOPE FOR FM AND CFIDS SUFFERERS
  • It's only ME, it's not my mind
  • Life as we know it
  • Living With Chronic Fatigue Syndrome
  • ME Agenda
  • Me Free For All
  • NMJ's velo gubbed legs
  • R.E.S.C.I.N.D.
  • SOPHIA AND M.E.
  • ahummingbirdsguide
  • blogging not jogging
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About Dr Speedy.

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Dr Speedy
I am a doctor. I am also an ME patient unfortunately. Bedbound that is. So at the moment I’m in private practice so to speak.
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