Deans' stroke musings

Changing stroke rehab and research worldwide now.Time is Brain!Just think of all the trillions and trillions of neurons that DIE each day because there are NO effective hyperacute therapies besides tPA(only 12% effective). I have 493 posts on hyperacute therapy, enough for researchers to spend decades proving them out. These are my personal ideas and blog on stroke rehabilitation and stroke research. Do not attempt any of these without checking with your medical provider. Unless you join me in agitating, when you need these therapies they won't be there.

What this blog is for:

Shortly after getting out of the hospital and getting NO information on the process or protocols of stroke rehabilitation and recovery I started searching on the internet and found that no other survivor received useful information. This is an attempt to cover all stroke rehabilitation information that should be readily available to survivors so they can talk with informed knowledge to their medical staff. It's quite disgusting that this information is not available from every stroke association and doctors group.
My back ground story is here:

Tuesday, August 1, 2017

Study sheds light on chronic fatigue syndrome

Would this help solve the stroke fatigue problem? We'll never know since we have NO stroke leadership and NO stroke strategy to get all survivors 100% recovered.
50% of stroke survivors have fatigue. What the fuck are your doctors doing to cure that?
A new study by a team of researchers from Stanford University sheds light on chronic fatigue syndrome, an ailment estimated to affect over 836,000 Americans that has no known cure or cause, according to the U.S. Centers for Disease Control and Prevention.
Chronic fatigue syndrome (sometimes referred to in medical literature by the acronym ME/CFS for myalgic encephalomyelitis/chronic fatigue syndrome) is a debilitating illness characterized by overwhelming fatigue that is not improved by rest, according to the CDC.
The cause of ME/CFS has baffled researchers for decades, and the CDC estimates that approximately 90 percent of people with ME/CFS have not been diagnosed.
“Chronic fatigue syndrome can turn a life of productive activity into one of dependency and desolation,” Jose Montoya, M.D., lead author of the new study, published Monday in the Proceedings of the National Academy of Sciences, said in a statement.
The study found that people with chronic fatigue syndrome had substantially higher levels of certain cytokines, substances from the immune system, in their blood. Researchers found that the higher the levels of certain pro-inflammatory cytokines, the more severe the symptoms of chronic fatigue syndrome symptom were in a patient, and suggested there is a link between excess inflammation and the disease.
“There’s been a great deal of controversy and confusion surrounding ME/CFS -- even whether it is an actual disease,” the study's senior author, Mark Davis, Ph.D. said in a statement, adding that the new research provides "a solid basis for a diagnostic blood test."
ABC News' senior medical contributor Dr. Jennifer Ashton said that the study should encourage patients with ME/CFS that researchers have not ignored their pain, even if many questions surrounding the disease still remain.
The new research may also encourage patients who have felt like the disease was all in their heads.
“I have seen the horrors of this disease, multiplied by hundreds of patients,” Montoya said in a statement. “It’s been observed and talked about for 35 years now, sometimes with the onus of being described as a psychological condition. But chronic fatigue syndrome is by no means a figment of the imagination. This is real.”

No comments:

Post a Comment