• Welcome to Phoenix Rising!

    Created in 2008, Phoenix Rising is the largest and oldest forum dedicated to furthering the understanding of, and finding treatments for, complex chronic illnesses such as chronic fatigue syndrome (ME/CFS), fibromyalgia, long COVID, postural orthostatic tachycardia syndrome (POTS), mast cell activation syndrome (MCAS), and allied diseases.

    To become a member, simply click the Register button at the top right.

Article: British Medical Journal Published: 11th Feb 2010

Don't forget to post comments on the BMJ website http://www.bmj.com/cgi/eletter-submit/340/feb11_1/c738 . It isn't easy of course to get into the print version but it's not to hard to get a comment up on the site.It probably helps to make it look at least a little like a medical letter e.g. have at least one reference. Of course, one easy reference is the article itself (1). Or even a website (2).References:1. Santhouse AM, Hotopf M, David AS. Chronic Fatigue Syndrome. BMJ 2010;340:c738 2. www.samplewebsite.com (last accessed: 11 February 2010)
 
M
Doctors are not getting an accurate diagnosis, as some things are not 'what the numbers' indicate. They are dealing with multiple autoimmune issues.Consider gamma globulin, Rituxan, whole blood cell transfusions and glyconutrients for help.Another cause of very high white blood cell counts is when there is AIHA. The autoimmune action on the red blood cells stimulates production of white blood cells. Autoimmune Hemolytic Anemia is more common than we realize http://www.valdezlink.com/re/health/anemia/comment.htm#ofExposure to glycol ether 'looks like' the flu.
 
It is interesting how often 'chronic fatigue' is used in place of CFS. IMHO, the only reason there is unclear treatments is because there is no valid scientific research looking for contributing factors; there is only an assumption of psychological factors, not born out by double-blinded control studies. It is not acknowledged that even if a PWC/ME is depressed, they many times are adversely affected by the doses required to treat it, solely because of the underlying CFS/ME. This is all psychobabble to me.
 
BMJ editorial in Irish Medical Times

http://www.imt.ie/clinical/infections-immunology/defeatism-undermines-treatment.html

The Irish MedicalTimes is a free weekly newspaper sent to Irish doctors.

People can comment online.

If you want to send a letter, send it to: editor@imt.ie.
Letters start: "Dear Editor".
Don't forget to put your name and contact number (although most times they won't ring).
400 words is about the max words I think but probably as you decrease from that, the chances it will be published will increase, especially if you're not a doctor and don't have any fancy title.