A CALL FOR ACTION: THE RECOGNITION OF MYALGIC ENCEPHALOMYELITIS AS A SERIOUS AND DEBILITATING DISEASE

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We, the undersigned, respectfully demand that Myalgic Encephalomyelitis (ME), an internationally recognized neurological disease, be also formally recognized as a distinct clinical entity in the United States by the National Institutes of Health and the Centers for Disease Control. It is time to make the case definition/diagnostic criteria explicit in the name.

Currently, most patients are diagnosed with Chronic Fatigue Syndrome, a poorly defined, misunderstood, controversial syndrome which remains underfunded and underresearched. The name Chronic Fatigue Syndrome itself has trivialized the illness and further subjected these patients to incredulity and ridicule. The CFS rubric has not only neglected and failed to help those with ME, it has harmed them. ME patients will not improve with cognitive behavioral therapy (CBT) or graded exercise (in fact, exercise will make them worse) - yet these are considered treatments for CFS. Simply "renaming" CFS will not solve this problem.

ME should not be considered a subset of CFS, for the hallmarks of ME will not be present in the population of CFS patients once the Ramsay criteria are established in the US. Patients with Myalgic Encephalomyelitis under the CFS criteria must wait for six (6) months before acquiring a diagnosis, a critical period in which possible recovery is diminished by lack of proper treatment. The ME definition does not require a six month wait. (See Ramsay Definition at: http://www.egroups.co.uk/message/ME-itis_NOW/2.)

We, the undersigned, are "tired of being sick, not sick of being tired."



To read a complete discussion of the points outlined here, we suggest you
visit http://www.egroups.co.uk/message/ME-itis_NOW/
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1,000 signatures
Goal: 5,000
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29 February 2016
1000. Deborah Lc | I support this petition
27 February 2016
999. Dave S | it is so painful losing your ability to live especially married with children Country/State usa
21 February 2016
998. Myra P | No one knows until they themselves have been there/ Country/State Alabama
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996. Judith A | also help fibromyalgia patients with their excrutiating pain from which I personally suffer. Country/State Dearborn Heights Michigan
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985. Karen M | We need Help! Country/State USA
20 December 2015
984. Diane M | I support this petition
19 December 2015
983. David K | I support this petition
18 December 2015
982. Gail B | I am a 16 year sufferer of this terrible illness. The indignation and humiliation I have suffered because of the name Chronic Fatigue is intolerable. Please change the name back to ME where it belongs. All of my symptoms are the symptoms of ME - NOT JUST
13 December 2015
981. Cynthia Lc | I support this petition
9 December 2015
980. Christine S | I support this petition
8 December 2015
979. Emma E | I support this petition
8 December 2015
978. Julie Em | I am one of the many who have suffered due to the trivialization of, and lack of adequate research and treatment resources for, this disease. Country/State USA/MA
1 December 2015
977. Sandra M | I support this petition
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976. Tammy W | I support this petition
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Petition target:
United States Department of Health and Human Services, National Institutes of Health, and Centers for Disease Control
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